Project acronym 2DHIBSA
Project Nanoscopic and Hierachical Materials via Living Crystallization-Driven Self-Assembly
Researcher (PI) Ian MANNERS
Host Institution (HI) UNIVERSITY OF BRISTOL
Call Details Advanced Grant (AdG), PE5, ERC-2017-ADG
Summary A key synthetic challenge of widespread interest in chemical science involves the creation of well-defined 2D functional materials that exist on a length-scale of nanometers to microns. In this ambitious 5 year proposal we aim to tackle this issue by exploiting the unique opportunities made possible by recent developments with the living crystallization-driven self-assembly (CDSA) platform. Using this solution processing approach, amphiphilic block copolymers (BCPs) with crystallizable blocks, related amphiphiles, and polymers with charged end groups will be used to predictably construct monodisperse samples of tailored, functional soft matter-based 2D nanostructures with controlled shape, size, and spatially-defined chemistries. Many of the resulting nanostructures will also offer unprecedented opportunities as precursors to materials with hierarchical structures through further solution-based “bottom-up” assembly methods. In addition to fundamental studies, the proposed work also aims to make important impact in the cutting-edge fields of liquid crystals, interface stabilization, catalysis, supramolecular polymers, and hierarchical materials.
Summary
A key synthetic challenge of widespread interest in chemical science involves the creation of well-defined 2D functional materials that exist on a length-scale of nanometers to microns. In this ambitious 5 year proposal we aim to tackle this issue by exploiting the unique opportunities made possible by recent developments with the living crystallization-driven self-assembly (CDSA) platform. Using this solution processing approach, amphiphilic block copolymers (BCPs) with crystallizable blocks, related amphiphiles, and polymers with charged end groups will be used to predictably construct monodisperse samples of tailored, functional soft matter-based 2D nanostructures with controlled shape, size, and spatially-defined chemistries. Many of the resulting nanostructures will also offer unprecedented opportunities as precursors to materials with hierarchical structures through further solution-based “bottom-up” assembly methods. In addition to fundamental studies, the proposed work also aims to make important impact in the cutting-edge fields of liquid crystals, interface stabilization, catalysis, supramolecular polymers, and hierarchical materials.
Max ERC Funding
2 499 597 €
Duration
Start date: 2018-05-01, End date: 2023-04-30
Project acronym 3DIMAGE
Project 3D Imaging Across Lengthscales: From Atoms to Grains
Researcher (PI) Paul Anthony Midgley
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Advanced Grant (AdG), PE4, ERC-2011-ADG_20110209
Summary "Understanding structure-property relationships across lengthscales is key to the design of functional and structural materials and devices. Moreover, the complexity of modern devices extends to three dimensions and as such 3D characterization is required across those lengthscales to provide a complete understanding and enable improvement in the material’s physical and chemical behaviour. 3D imaging and analysis from the atomic scale through to granular microstructure is proposed through the development of electron tomography using (S)TEM, and ‘dual beam’ SEM-FIB, techniques offering complementary approaches to 3D imaging across lengthscales stretching over 5 orders of magnitude.
We propose to extend tomography to include novel methods to determine atom positions in 3D with approaches incorporating new reconstruction algorithms, image processing and complementary nano-diffraction techniques. At the nanoscale, true 3D nano-metrology of morphology and composition is a key objective of the project, minimizing reconstruction and visualization artefacts. Mapping strain and optical properties in 3D are ambitious and exciting challenges that will yield new information at the nanoscale. Using the SEM-FIB, 3D ‘mesoscale’ structures will be revealed: morphology, crystallography and composition can be mapped simultaneously, with ~5nm resolution and over volumes too large to tackle by (S)TEM and too small for most x-ray techniques. In parallel, we will apply 3D imaging to a wide variety of key materials including heterogeneous catalysts, aerospace alloys, biomaterials, photovoltaic materials, and novel semiconductors.
We will collaborate with many departments in Cambridge and institutes worldwide. The personnel on the proposal will cover all aspects of the tomography proposed using high-end TEMs, including an aberration-corrected Titan, and a Helios dual beam. Importantly, a postdoc is dedicated to developing new algorithms for reconstruction, image and spectral processing."
Summary
"Understanding structure-property relationships across lengthscales is key to the design of functional and structural materials and devices. Moreover, the complexity of modern devices extends to three dimensions and as such 3D characterization is required across those lengthscales to provide a complete understanding and enable improvement in the material’s physical and chemical behaviour. 3D imaging and analysis from the atomic scale through to granular microstructure is proposed through the development of electron tomography using (S)TEM, and ‘dual beam’ SEM-FIB, techniques offering complementary approaches to 3D imaging across lengthscales stretching over 5 orders of magnitude.
We propose to extend tomography to include novel methods to determine atom positions in 3D with approaches incorporating new reconstruction algorithms, image processing and complementary nano-diffraction techniques. At the nanoscale, true 3D nano-metrology of morphology and composition is a key objective of the project, minimizing reconstruction and visualization artefacts. Mapping strain and optical properties in 3D are ambitious and exciting challenges that will yield new information at the nanoscale. Using the SEM-FIB, 3D ‘mesoscale’ structures will be revealed: morphology, crystallography and composition can be mapped simultaneously, with ~5nm resolution and over volumes too large to tackle by (S)TEM and too small for most x-ray techniques. In parallel, we will apply 3D imaging to a wide variety of key materials including heterogeneous catalysts, aerospace alloys, biomaterials, photovoltaic materials, and novel semiconductors.
We will collaborate with many departments in Cambridge and institutes worldwide. The personnel on the proposal will cover all aspects of the tomography proposed using high-end TEMs, including an aberration-corrected Titan, and a Helios dual beam. Importantly, a postdoc is dedicated to developing new algorithms for reconstruction, image and spectral processing."
Max ERC Funding
2 337 330 €
Duration
Start date: 2012-01-01, End date: 2017-12-31
Project acronym ADOR
Project Assembly-disassembly-organisation-reassembly of microporous materials
Researcher (PI) Russell MORRIS
Host Institution (HI) THE UNIVERSITY COURT OF THE UNIVERSITY OF ST ANDREWS
Call Details Advanced Grant (AdG), PE5, ERC-2017-ADG
Summary Microporous materials are an important class of solid; the two main members of this family are zeolites and metal-organic frameworks (MOFs). Zeolites are industrial solids whose applications range from catalysis, through ion exchange and adsorption technologies to medicine. MOFs are some of the most exciting new materials to have been developed over the last two decades, and they are just beginning to be applied commercially.
Over recent years the applicant’s group has developed new synthetic strategies to prepare microporous materials, called the Assembly-Disassembly-Organisation-Reassembly (ADOR) process. In significant preliminary work the ADOR process has shown to be an extremely important new synthetic methodology that differs fundamentally from traditional solvothermal methods.
In this project I will look to overturn the conventional thinking in materials science by developing methodologies that can target both zeolites and MOF materials that are difficult to prepare using traditional methods – the so-called ‘unfeasible’ materials. The importance of such a new methodology is that it will open up routes to materials that have different properties (both chemical and topological) to those we currently have. Since zeolites and MOFs have so many actual and potential uses, the preparation of materials with different properties has a high chance of leading to new technologies in the medium/long term. To complete the major objective I will look to complete four closely linked activities covering the development of design strategies for zeolites and MOFs (activities 1 & 2), mechanistic studies to understand the process at the molecular level using in situ characterisation techniques (activity 3) and an exploration of potential applied science for the prepared materials (activity 4).
Summary
Microporous materials are an important class of solid; the two main members of this family are zeolites and metal-organic frameworks (MOFs). Zeolites are industrial solids whose applications range from catalysis, through ion exchange and adsorption technologies to medicine. MOFs are some of the most exciting new materials to have been developed over the last two decades, and they are just beginning to be applied commercially.
Over recent years the applicant’s group has developed new synthetic strategies to prepare microporous materials, called the Assembly-Disassembly-Organisation-Reassembly (ADOR) process. In significant preliminary work the ADOR process has shown to be an extremely important new synthetic methodology that differs fundamentally from traditional solvothermal methods.
In this project I will look to overturn the conventional thinking in materials science by developing methodologies that can target both zeolites and MOF materials that are difficult to prepare using traditional methods – the so-called ‘unfeasible’ materials. The importance of such a new methodology is that it will open up routes to materials that have different properties (both chemical and topological) to those we currently have. Since zeolites and MOFs have so many actual and potential uses, the preparation of materials with different properties has a high chance of leading to new technologies in the medium/long term. To complete the major objective I will look to complete four closely linked activities covering the development of design strategies for zeolites and MOFs (activities 1 & 2), mechanistic studies to understand the process at the molecular level using in situ characterisation techniques (activity 3) and an exploration of potential applied science for the prepared materials (activity 4).
Max ERC Funding
2 489 220 €
Duration
Start date: 2018-10-01, End date: 2023-09-30
Project acronym AFRIGOS
Project African Governance and Space: Transport Corridors, Border Towns and Port Cities in Transition
Researcher (PI) Paul Christopher Nugent
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Advanced Grant (AdG), SH2, ERC-2014-ADG
Summary AFRIGOS investigates the process of 'respacing' Africa, a political drive towards regional and continental integration, on the one hand, and the re-casting of Africa's engagement with the global economy, on the other. This is reflected in unprecedented levels of investment in physical and communications infrastructure, and the outsourcing of key functions of Customs, Immigration and security agencies. AFRIGOS poses the question of how far respacing is genuinely forging institutions that are facilitating or obstructing the movement of people and goods; that are enabling or preventing urban and border spaces from being more effectively and responsively governed; and that take into account the needs of African populations whose livelihoods are rooted in mobility and informality. The principal research questions are approached through a comparative study of port cities, border towns and other strategic nodes situated along the busiest transport corridors in East, Central, West and Southern Africa. These represent sites of remarkable dynamism and cosmopolitanism, which reflects their role in connecting African urban centres to each other and to other global cities.
AFRIGOS considers how governance 'assemblages' are forged at different scales and is explicitly comparative. It works through 5 connected Streams that address specific questions: 1. AGENDA-SETTING is concerned with policy (re-)formulation. 2. PERIPHERAL URBANISM examines governance in border towns and port cities. 3. BORDER WORKERS addresses everyday governance emerging through the interaction of officials and others who make their livelihoods from the border. 4. CONNECTIVE INFRASTRUCTURE looks as the transformative effects of new technologies. 5. PEOPLE & GOODS IN MOTION traces the passage of people and goods and the regimes of regulation to which they are subjected. AFRIGOS contributes to interdisciplinary research on borderland studies, multi-level governance and the everyday state.
Summary
AFRIGOS investigates the process of 'respacing' Africa, a political drive towards regional and continental integration, on the one hand, and the re-casting of Africa's engagement with the global economy, on the other. This is reflected in unprecedented levels of investment in physical and communications infrastructure, and the outsourcing of key functions of Customs, Immigration and security agencies. AFRIGOS poses the question of how far respacing is genuinely forging institutions that are facilitating or obstructing the movement of people and goods; that are enabling or preventing urban and border spaces from being more effectively and responsively governed; and that take into account the needs of African populations whose livelihoods are rooted in mobility and informality. The principal research questions are approached through a comparative study of port cities, border towns and other strategic nodes situated along the busiest transport corridors in East, Central, West and Southern Africa. These represent sites of remarkable dynamism and cosmopolitanism, which reflects their role in connecting African urban centres to each other and to other global cities.
AFRIGOS considers how governance 'assemblages' are forged at different scales and is explicitly comparative. It works through 5 connected Streams that address specific questions: 1. AGENDA-SETTING is concerned with policy (re-)formulation. 2. PERIPHERAL URBANISM examines governance in border towns and port cities. 3. BORDER WORKERS addresses everyday governance emerging through the interaction of officials and others who make their livelihoods from the border. 4. CONNECTIVE INFRASTRUCTURE looks as the transformative effects of new technologies. 5. PEOPLE & GOODS IN MOTION traces the passage of people and goods and the regimes of regulation to which they are subjected. AFRIGOS contributes to interdisciplinary research on borderland studies, multi-level governance and the everyday state.
Max ERC Funding
2 491 364 €
Duration
Start date: 2016-01-01, End date: 2020-12-31
Project acronym AFTERTHEGOLDRUSH
Project Addressing global sustainability challenges by changing perceptions in catalyst design
Researcher (PI) Graham John Hutchings
Host Institution (HI) CARDIFF UNIVERSITY
Call Details Advanced Grant (AdG), PE4, ERC-2011-ADG_20110209
Summary One of the greatest challenges facing society is the sustainability of resources. At present, a step change in the sustainable use of resources is needed and catalysis lies at the heart of the solution by providing new routes to carbon dioxide mitigation, energy security and water conservation. It is clear that new high efficiency game-changing catalysts are required to meet the challenge. This proposal will focus on excellence in catalyst design by learning from recent step change advances in gold catalysis by challenging perceptions. Intense interest in gold catalysts over the past two decades has accelerated our understanding of gold particle-size effects, gold-support and gold-metal interactions, the interchange between atomic and ionic gold species, and the role of the gold-support interface in creating and maintaining catalytic activity. The field has also driven the development of cutting-edge techniques, particularly in microscopy and transient kinetics, providing detailed structural characterisation on the nano-scale and probing the short-range and often short-lived interactions. By comparison, our understanding of other metal catalysts has remained relatively static.
The proposed programme will engender a step change in the design of supported-metal catalysts, by exploiting the learning and the techniques emerging from gold catalysis. The research will be set out in two themes. In Theme 1 two established key grand challenges will be attacked; namely, energy vectors and greenhouse gas control. Theme 2 will address two new and emerging grand challenges in catalysis namely the effective low temperature activation of primary carbon hydrogen bonds and CO2 utilisation where instead of treating CO2 as a thermodynamic endpoint, the aim will be to re-use it as a feedstock for bulk chemical and fuel production. The legacy of the research will be the development of a new catalyst design approach that will provide a tool box for future catalyst development.
Summary
One of the greatest challenges facing society is the sustainability of resources. At present, a step change in the sustainable use of resources is needed and catalysis lies at the heart of the solution by providing new routes to carbon dioxide mitigation, energy security and water conservation. It is clear that new high efficiency game-changing catalysts are required to meet the challenge. This proposal will focus on excellence in catalyst design by learning from recent step change advances in gold catalysis by challenging perceptions. Intense interest in gold catalysts over the past two decades has accelerated our understanding of gold particle-size effects, gold-support and gold-metal interactions, the interchange between atomic and ionic gold species, and the role of the gold-support interface in creating and maintaining catalytic activity. The field has also driven the development of cutting-edge techniques, particularly in microscopy and transient kinetics, providing detailed structural characterisation on the nano-scale and probing the short-range and often short-lived interactions. By comparison, our understanding of other metal catalysts has remained relatively static.
The proposed programme will engender a step change in the design of supported-metal catalysts, by exploiting the learning and the techniques emerging from gold catalysis. The research will be set out in two themes. In Theme 1 two established key grand challenges will be attacked; namely, energy vectors and greenhouse gas control. Theme 2 will address two new and emerging grand challenges in catalysis namely the effective low temperature activation of primary carbon hydrogen bonds and CO2 utilisation where instead of treating CO2 as a thermodynamic endpoint, the aim will be to re-use it as a feedstock for bulk chemical and fuel production. The legacy of the research will be the development of a new catalyst design approach that will provide a tool box for future catalyst development.
Max ERC Funding
2 279 785 €
Duration
Start date: 2012-04-01, End date: 2017-03-31
Project acronym AISMA
Project An anthropological investigation of muscular politics in South Asia
Researcher (PI) Lucia Michelutti
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary Over the past decade, the media, international organisations, as well as policy-making bodies have voiced increasing concern about a growing overlap between the criminal and political spheres in South Asia. Many 'criminal politicians' are accused not simply of embezzlement, but of burglary, kidnapping and murder, so that the observed political landscape emerges not only as a 'corrupt', but also a highly violent sphere. This project is a collaborative and cross-national ethnographic study of the criminalisation of politics in India, Pakistan and Bangladesh. Bringing together local-level investigation, surveys and historical analysis, the project will produce comprehensive political ethnographies in sixteen sites across the subcontinent, providing empirical material and theoretical directives for further charting of the virtually unexplored terrain of extra-legal muscular politics in the region. Central to the proposed programme of research are the following interrelated objectives: 1) To further develop the method of collaborative political ethnography by designing, collecting and producing case studies which will allow us to write thematically across sites; 2) To generate policy relevant research in the fields of security, conflict, democracy and development; 3) To produce capability by forging an international network of scholars on issues related to democratisation, violence, crime and support the work and careers of the project's 4 Post-docs. The study capitalises on previous research and skills of the PI in the cross-cultural study of democracy and muscular politics in the global South. All members of the research team have expertise in ethnographic research in the difficult spheres of criminal politics, informal economies, and political violence and are hence well and sometimes uniquely equipped to pursue this challenging research thematic.
Summary
Over the past decade, the media, international organisations, as well as policy-making bodies have voiced increasing concern about a growing overlap between the criminal and political spheres in South Asia. Many 'criminal politicians' are accused not simply of embezzlement, but of burglary, kidnapping and murder, so that the observed political landscape emerges not only as a 'corrupt', but also a highly violent sphere. This project is a collaborative and cross-national ethnographic study of the criminalisation of politics in India, Pakistan and Bangladesh. Bringing together local-level investigation, surveys and historical analysis, the project will produce comprehensive political ethnographies in sixteen sites across the subcontinent, providing empirical material and theoretical directives for further charting of the virtually unexplored terrain of extra-legal muscular politics in the region. Central to the proposed programme of research are the following interrelated objectives: 1) To further develop the method of collaborative political ethnography by designing, collecting and producing case studies which will allow us to write thematically across sites; 2) To generate policy relevant research in the fields of security, conflict, democracy and development; 3) To produce capability by forging an international network of scholars on issues related to democratisation, violence, crime and support the work and careers of the project's 4 Post-docs. The study capitalises on previous research and skills of the PI in the cross-cultural study of democracy and muscular politics in the global South. All members of the research team have expertise in ethnographic research in the difficult spheres of criminal politics, informal economies, and political violence and are hence well and sometimes uniquely equipped to pursue this challenging research thematic.
Max ERC Funding
1 200 000 €
Duration
Start date: 2012-03-01, End date: 2016-02-29
Project acronym AlCat
Project Bond activation and catalysis with low-valent aluminium
Researcher (PI) Michael James COWLEY
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Starting Grant (StG), PE5, ERC-2016-STG
Summary This project will develop the principles required to enable bond-modifying redox catalysis based on aluminium by preparing and studying new Al(I) compounds capable of reversible oxidative addition.
Catalytic processes are involved in the synthesis of 75 % of all industrially produced chemicals, but most catalysts involved are based on precious metals such as rhodium, palladium or platinum. These metals are expensive and their supply limited and unstable; there is a significant need to develop the chemistry of non-precious metals as alternatives. On toxicity and abundance alone, aluminium is an attractive candidate. Furthermore, recent work, including in our group, has demonstrated that Al(I) compounds can perform a key step in catalytic cycles - the oxidative addition of E-H bonds.
In order to realise the significant potential of Al(I) for transition-metal style catalysis we urgently need to:
- establish the principles governing oxidative addition and reductive elimination reactivity in aluminium systems.
- know how the reactivity of Al(I) compounds can be controlled by varying properties of ligand frameworks.
- understand the onward reactivity of oxidative addition products of Al(I) to enable applications in catalysis.
In this project we will:
- Study mechanisms of oxidative addition and reductive elimination of a range of synthetically relevant bonds at Al(I) centres, establishing the principles governing this fundamental reactivity.
- Develop new ligand frameworks to support of Al(I) centres and evaluate the effect of the ligand on oxidative addition/reductive elimination at Al centres.
- Investigate methods for Al-mediated functionalisation of organic compounds by exploring the reactivity of E-H oxidative addition products with unsaturated organic compounds.
Summary
This project will develop the principles required to enable bond-modifying redox catalysis based on aluminium by preparing and studying new Al(I) compounds capable of reversible oxidative addition.
Catalytic processes are involved in the synthesis of 75 % of all industrially produced chemicals, but most catalysts involved are based on precious metals such as rhodium, palladium or platinum. These metals are expensive and their supply limited and unstable; there is a significant need to develop the chemistry of non-precious metals as alternatives. On toxicity and abundance alone, aluminium is an attractive candidate. Furthermore, recent work, including in our group, has demonstrated that Al(I) compounds can perform a key step in catalytic cycles - the oxidative addition of E-H bonds.
In order to realise the significant potential of Al(I) for transition-metal style catalysis we urgently need to:
- establish the principles governing oxidative addition and reductive elimination reactivity in aluminium systems.
- know how the reactivity of Al(I) compounds can be controlled by varying properties of ligand frameworks.
- understand the onward reactivity of oxidative addition products of Al(I) to enable applications in catalysis.
In this project we will:
- Study mechanisms of oxidative addition and reductive elimination of a range of synthetically relevant bonds at Al(I) centres, establishing the principles governing this fundamental reactivity.
- Develop new ligand frameworks to support of Al(I) centres and evaluate the effect of the ligand on oxidative addition/reductive elimination at Al centres.
- Investigate methods for Al-mediated functionalisation of organic compounds by exploring the reactivity of E-H oxidative addition products with unsaturated organic compounds.
Max ERC Funding
1 493 679 €
Duration
Start date: 2017-03-01, End date: 2022-02-28
Project acronym ALIGN
Project Ab-initio computational modelling of photovoltaic interfaces
Researcher (PI) Feliciano Giustino
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), PE5, ERC-2009-StG
Summary The aim of the ALIGN project is to understand, predict, and optimize the photovoltaic energy conversion in third-generation solar cells, starting from an atomic-scale quantum-mechanical modelling of the photovoltaic interface. The quest for photovoltaic materials suitable for low-cost synthesis, large-area production, and functional architecture has driven substantial research efforts towards third-generation photovoltaic devices such as plastic solar cells, organic-inorganic cells, and photo-electrochemical cells. The physical and chemical processes involved in the harvesting of sunlight, the transport of electrical charge, and the build-up of the photo-voltage in these devices are fundamentally different from those encountered in traditional semiconductor heterojunction solar cells. A detailed atomic-scale quantum-mechanical description of such processes will lay down the basis for a rational approach to the modelling, optimization, and design of new photovoltaic materials. The short name of the proposal hints at one of the key materials parameters in the area of photovoltaic interfaces: the alignment of the quantum energy levels between the light-absorbing material and the electron acceptor. The level alignment drives the separation of the electron-hole pairs formed upon absorption of sunlight, and determines the open circuit voltage of the solar cell. The energy level alignment not only represents a key parameter for the design of photovoltaic devices, but also constitutes one of the grand challenges of modern computational materials science. Within this project we will develop and apply new ground-breaking computational methods to understand, predict, and optimize the energy level alignment and other design parameters of third-generation photovoltaic devices.
Summary
The aim of the ALIGN project is to understand, predict, and optimize the photovoltaic energy conversion in third-generation solar cells, starting from an atomic-scale quantum-mechanical modelling of the photovoltaic interface. The quest for photovoltaic materials suitable for low-cost synthesis, large-area production, and functional architecture has driven substantial research efforts towards third-generation photovoltaic devices such as plastic solar cells, organic-inorganic cells, and photo-electrochemical cells. The physical and chemical processes involved in the harvesting of sunlight, the transport of electrical charge, and the build-up of the photo-voltage in these devices are fundamentally different from those encountered in traditional semiconductor heterojunction solar cells. A detailed atomic-scale quantum-mechanical description of such processes will lay down the basis for a rational approach to the modelling, optimization, and design of new photovoltaic materials. The short name of the proposal hints at one of the key materials parameters in the area of photovoltaic interfaces: the alignment of the quantum energy levels between the light-absorbing material and the electron acceptor. The level alignment drives the separation of the electron-hole pairs formed upon absorption of sunlight, and determines the open circuit voltage of the solar cell. The energy level alignment not only represents a key parameter for the design of photovoltaic devices, but also constitutes one of the grand challenges of modern computational materials science. Within this project we will develop and apply new ground-breaking computational methods to understand, predict, and optimize the energy level alignment and other design parameters of third-generation photovoltaic devices.
Max ERC Funding
1 000 000 €
Duration
Start date: 2010-03-01, End date: 2016-02-29
Project acronym ALREG
Project Analysing Learning in Regulatory Governance
Researcher (PI) Claudio Radaelli
Host Institution (HI) THE UNIVERSITY OF EXETER
Call Details Advanced Grant (AdG), SH2, ERC-2008-AdG
Summary This four-year interdisciplinary project addresses the question what has been learned through the use of better regulation ? Better regulation is a flagship policy on the Lisbon agenda for growth and jobs. Its aims are to provide new governance architectures for law-making, to increase the competitiveness of the regulatory environment, and to secure wide social legitimacy for multi-level systems of rules. Whilst most of the research has looked at how better regulation is changing, this project will produce findings on what has changed because of better regulation. Theoretically, the project will use (and significantly improve on) theories of policy learning. Empirically, it will cover Denmark, Italy, the Netherlands, Poland, the UK and the EU including multi-level analysis and analysis by sector of regulation. Methodologically, the project will draw on comparative analysis of types of learning, experiments with regulatory policy-makers in six countries and the European Commission, large-n analysis of impact assessments, backward-mapping of legislation (to appraise the role played by better regulation in the formulation or laws in the UK and the EU), meta-analysis of case-studies and co-production of knowledge with better regulation officers. Dissemination will target both stakeholders (i.e., policy officers, civil society organizations, and business federations) and academic conferences in political science, law, and risk analysis, with a major research monograph to be completed in year 4 and a final interdisciplinary conference.
Summary
This four-year interdisciplinary project addresses the question what has been learned through the use of better regulation ? Better regulation is a flagship policy on the Lisbon agenda for growth and jobs. Its aims are to provide new governance architectures for law-making, to increase the competitiveness of the regulatory environment, and to secure wide social legitimacy for multi-level systems of rules. Whilst most of the research has looked at how better regulation is changing, this project will produce findings on what has changed because of better regulation. Theoretically, the project will use (and significantly improve on) theories of policy learning. Empirically, it will cover Denmark, Italy, the Netherlands, Poland, the UK and the EU including multi-level analysis and analysis by sector of regulation. Methodologically, the project will draw on comparative analysis of types of learning, experiments with regulatory policy-makers in six countries and the European Commission, large-n analysis of impact assessments, backward-mapping of legislation (to appraise the role played by better regulation in the formulation or laws in the UK and the EU), meta-analysis of case-studies and co-production of knowledge with better regulation officers. Dissemination will target both stakeholders (i.e., policy officers, civil society organizations, and business federations) and academic conferences in political science, law, and risk analysis, with a major research monograph to be completed in year 4 and a final interdisciplinary conference.
Max ERC Funding
948 448 €
Duration
Start date: 2009-09-01, End date: 2013-09-30
Project acronym AMPRO
Project Advanced Electronic Materials and Devices through Novel Processing Paradigms
Researcher (PI) Thomas Anthopoulos
Host Institution (HI) IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Call Details Starting Grant (StG), PE5, ERC-2011-StG_20101014
Summary "I propose a structured multidisciplinary research programme that seeks to combine advanced materials, such as metal oxides and organics, with novel fabrication methods to develop devices for application in: (1) large area electronics, (2) integrated nanoelectronics and (3) sensors. At the heart of this programme lies the development of novel oxide semiconductors. These will be synthesised from solution using precursors. Chemical doping via physical blending will be explored for the tuning of the electronic properties of these compounds. This simple approach will enable the rapid development of a library of materials far beyond those accessible by traditional methods. Oxides will then be combined with inorganic/organic dielectrics to demonstrate low power transistors. Ultimate target for application area (1) is the development of transistors with hole/electron mobilities exceeding 20/200 cm^2/Vs respectively. For application area (2) I will combine the precursor formulations with advanced scanning thermochemical nanolithography. A heated atomic force microscope tip will be used for the local chemical conversion of the precursor to oxide with sub-50 nm resolution. This will enable patterning of nanostructures with desirable shape and size. Sequential patterning of semi/conductive layers combined with SAM dielectrics would enable fabrication of nano-sized devices and circuits. For application area (3), research effort will focus on novel hybrid phototransistors. Use of different light absorbing organic dyes functionalised onto the oxide channel will be explored as a mean for developing high sensitivity phototransistors and full colour sensing arrays. Organic dyes will also be combined with nano-sized transistors to demonstrate integrated nano-scale optoelectronics. The unique combination of bottom-up and top-down strategies adopted in this project will lead to the development of novel high performance devices with a host of existing and new applications."
Summary
"I propose a structured multidisciplinary research programme that seeks to combine advanced materials, such as metal oxides and organics, with novel fabrication methods to develop devices for application in: (1) large area electronics, (2) integrated nanoelectronics and (3) sensors. At the heart of this programme lies the development of novel oxide semiconductors. These will be synthesised from solution using precursors. Chemical doping via physical blending will be explored for the tuning of the electronic properties of these compounds. This simple approach will enable the rapid development of a library of materials far beyond those accessible by traditional methods. Oxides will then be combined with inorganic/organic dielectrics to demonstrate low power transistors. Ultimate target for application area (1) is the development of transistors with hole/electron mobilities exceeding 20/200 cm^2/Vs respectively. For application area (2) I will combine the precursor formulations with advanced scanning thermochemical nanolithography. A heated atomic force microscope tip will be used for the local chemical conversion of the precursor to oxide with sub-50 nm resolution. This will enable patterning of nanostructures with desirable shape and size. Sequential patterning of semi/conductive layers combined with SAM dielectrics would enable fabrication of nano-sized devices and circuits. For application area (3), research effort will focus on novel hybrid phototransistors. Use of different light absorbing organic dyes functionalised onto the oxide channel will be explored as a mean for developing high sensitivity phototransistors and full colour sensing arrays. Organic dyes will also be combined with nano-sized transistors to demonstrate integrated nano-scale optoelectronics. The unique combination of bottom-up and top-down strategies adopted in this project will lead to the development of novel high performance devices with a host of existing and new applications."
Max ERC Funding
1 497 798 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym AnCon
Project A Comparative Anthropology of Conscience, Ethics and Human Rights
Researcher (PI) Tobias William Kelly
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Consolidator Grant (CoG), SH2, ERC-2014-CoG
Summary This project is a comparative anthropology of conscience, ethics and human rights. Numerous international human rights documents formally declare their commitment to protect freedom of conscience. But, what is conscience and how do we know it when we see it? How do we distinguish it from self-interest or fanaticism? And what happens when the concept, often associated with a distinct Christian or liberal history, travels across cultural boundaries? The project will examine the cultural conditions under which claims to conscience are made possible, and the types of claims that are most persuasive when doing so. The project addresses these issues through the comparative analysis of three case studies: British pacifists, Sri Lankan activists, and Soviet dissidents. These case studies have been carefully chosen to provide globally significant, but contrasting examples of contests over the implications of claims to conscience. If claims of conscience are often associated with a specifically liberal and Christian tradition, mid-twentieth century Britain can be said to stand at the centre of that tradition. Sri Lanka represents a particularly fraught post-colonial South Asian counterpoint, wracked by nationalist violence, and influenced by ethical traditions associated with forms of Hinduism and Buddhism. Soviet Russia represents a further contrast, a totalitarian regime, where atheism was the dominant ethical language. Finally, the project will return specifically to international human rights institutions, examining the history of the category of conscience in the UN human rights system. This project will be ground breaking, employing novel methods and analytical insights, in order to producing the first comparative analysis of the cultural and political salience of claims of conscience. In doing so, the research aims to transform our understandings of the limits and potentials of attempts to protect freedom of conscience.
Summary
This project is a comparative anthropology of conscience, ethics and human rights. Numerous international human rights documents formally declare their commitment to protect freedom of conscience. But, what is conscience and how do we know it when we see it? How do we distinguish it from self-interest or fanaticism? And what happens when the concept, often associated with a distinct Christian or liberal history, travels across cultural boundaries? The project will examine the cultural conditions under which claims to conscience are made possible, and the types of claims that are most persuasive when doing so. The project addresses these issues through the comparative analysis of three case studies: British pacifists, Sri Lankan activists, and Soviet dissidents. These case studies have been carefully chosen to provide globally significant, but contrasting examples of contests over the implications of claims to conscience. If claims of conscience are often associated with a specifically liberal and Christian tradition, mid-twentieth century Britain can be said to stand at the centre of that tradition. Sri Lanka represents a particularly fraught post-colonial South Asian counterpoint, wracked by nationalist violence, and influenced by ethical traditions associated with forms of Hinduism and Buddhism. Soviet Russia represents a further contrast, a totalitarian regime, where atheism was the dominant ethical language. Finally, the project will return specifically to international human rights institutions, examining the history of the category of conscience in the UN human rights system. This project will be ground breaking, employing novel methods and analytical insights, in order to producing the first comparative analysis of the cultural and political salience of claims of conscience. In doing so, the research aims to transform our understandings of the limits and potentials of attempts to protect freedom of conscience.
Max ERC Funding
1 457 869 €
Duration
Start date: 2015-08-01, End date: 2020-07-31
Project acronym ANGLE
Project Accelerated design and discovery of novel molecular materials via global lattice energy minimisation
Researcher (PI) Graeme Matthew Day
Host Institution (HI) UNIVERSITY OF SOUTHAMPTON
Call Details Starting Grant (StG), PE4, ERC-2012-StG_20111012
Summary The goal of crystal engineering is the design of functional crystalline materials in which the arrangement of basic structural building blocks imparts desired properties. The engineering of organic molecular crystals has, to date, relied largely on empirical rules governing the intermolecular association of functional groups in the solid state. However, many materials properties depend intricately on the complete crystal structure, i.e. the unit cell, space group and atomic positions, which cannot be predicted solely using such rules. Therefore, the development of computational methods for crystal structure prediction (CSP) from first principles has been a goal of computational chemistry that could significantly accelerate the design of new materials. It is only recently that the necessary advances in the modelling of intermolecular interactions and developments in algorithms for identifying all relevant crystal structures have come together to provide predictive methods that are becoming reliable and affordable on a timescale that could usefully complement an experimental research programme. The principle aim of the proposed work is to establish the use of state-of-the-art crystal structure prediction methods as a means of guiding the discovery and design of novel molecular materials.
This research proposal both continues the development of the computational methods for CSP and, by developing a computational framework for screening of potential molecules, develops the application of these methods for materials design. The areas on which we will focus are organic molecular semiconductors with high charge carrier mobilities and, building on our recently published results in Nature [1], the development of porous organic molecular materials. The project will both deliver novel materials, as well as improvements in the reliability of computational methods that will find widespread applications in materials chemistry.
[1] Nature 2011, 474, 367-371.
Summary
The goal of crystal engineering is the design of functional crystalline materials in which the arrangement of basic structural building blocks imparts desired properties. The engineering of organic molecular crystals has, to date, relied largely on empirical rules governing the intermolecular association of functional groups in the solid state. However, many materials properties depend intricately on the complete crystal structure, i.e. the unit cell, space group and atomic positions, which cannot be predicted solely using such rules. Therefore, the development of computational methods for crystal structure prediction (CSP) from first principles has been a goal of computational chemistry that could significantly accelerate the design of new materials. It is only recently that the necessary advances in the modelling of intermolecular interactions and developments in algorithms for identifying all relevant crystal structures have come together to provide predictive methods that are becoming reliable and affordable on a timescale that could usefully complement an experimental research programme. The principle aim of the proposed work is to establish the use of state-of-the-art crystal structure prediction methods as a means of guiding the discovery and design of novel molecular materials.
This research proposal both continues the development of the computational methods for CSP and, by developing a computational framework for screening of potential molecules, develops the application of these methods for materials design. The areas on which we will focus are organic molecular semiconductors with high charge carrier mobilities and, building on our recently published results in Nature [1], the development of porous organic molecular materials. The project will both deliver novel materials, as well as improvements in the reliability of computational methods that will find widespread applications in materials chemistry.
[1] Nature 2011, 474, 367-371.
Max ERC Funding
1 499 906 €
Duration
Start date: 2012-10-01, End date: 2017-09-30
Project acronym Arctic Domus
Project Arctic Domestication: Emplacing Human-Animal Relationships in the Circumpolar North
Researcher (PI) David George Anderson
Host Institution (HI) THE UNIVERSITY COURT OF THE UNIVERSITY OF ABERDEEN
Call Details Advanced Grant (AdG), SH2, ERC-2011-ADG_20110406
Summary This 6-year project aims to co-ordinate field research in each of these fields to elaborate a new model of emplaced human-animal relations evoking recent theoretical concerns of the definition of the person, the attribution of agency, and renewed attention to ‘built environments’. The project will work inductively from empirical observations in seven field sites across the circumpolar Arctic from the Russian Federation, to Fennoscandia, to Canada. The circumpolar Arctic originally provided many of the primary thought experiments for classic models of cultural evolution. It has now again become the focus of powerful debates over the balance between the protection of cultural heritage and the development of natural resources to fuel a future for industrial economies. The human-non-human relationships chosen for study cover the full range of theoretical and political discourse within the sciences today from primary encounters in domination to contemporary bio-technical innovations in farming. The team will transcend typical ‘existential’ models of domination between people and animals by describing complex social settings where more than one species interact with the cultural landscape. The team will also challenge existing definitions between wild and tame by instead examining what links these behaviour types together. Further, the team members will examine how domestication was never a sudden, fleeting intuition but rather a process wherein people and domesticates are sometimes closer and sometimes farther from each other. Finally, the research team, working within the above mentioned literatures, will develop a renewed model – a new way of describing – these relationships which does not necessarily rely upon metaphors of domination, competition, individual struggle, origins, or hybridity. The strength of the team, and the principle investigator, is their demonstrated ability to carry out fieldwork in this often difficult to access region.
Summary
This 6-year project aims to co-ordinate field research in each of these fields to elaborate a new model of emplaced human-animal relations evoking recent theoretical concerns of the definition of the person, the attribution of agency, and renewed attention to ‘built environments’. The project will work inductively from empirical observations in seven field sites across the circumpolar Arctic from the Russian Federation, to Fennoscandia, to Canada. The circumpolar Arctic originally provided many of the primary thought experiments for classic models of cultural evolution. It has now again become the focus of powerful debates over the balance between the protection of cultural heritage and the development of natural resources to fuel a future for industrial economies. The human-non-human relationships chosen for study cover the full range of theoretical and political discourse within the sciences today from primary encounters in domination to contemporary bio-technical innovations in farming. The team will transcend typical ‘existential’ models of domination between people and animals by describing complex social settings where more than one species interact with the cultural landscape. The team will also challenge existing definitions between wild and tame by instead examining what links these behaviour types together. Further, the team members will examine how domestication was never a sudden, fleeting intuition but rather a process wherein people and domesticates are sometimes closer and sometimes farther from each other. Finally, the research team, working within the above mentioned literatures, will develop a renewed model – a new way of describing – these relationships which does not necessarily rely upon metaphors of domination, competition, individual struggle, origins, or hybridity. The strength of the team, and the principle investigator, is their demonstrated ability to carry out fieldwork in this often difficult to access region.
Max ERC Funding
2 497 830 €
Duration
Start date: 2012-07-01, End date: 2018-06-30
Project acronym ARTEFACT
Project The Global as Artefact: Understanding the Patterns of Global Political History Through an Anthropology of Knowledge -- The Case of Agriculture in Four Global Systems from the Neolithic to the Present
Researcher (PI) INANNA HAMATI-ATAYA
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Consolidator Grant (CoG), SH2, ERC-2016-COG
Summary Knowledge is an anthropological constant that is indissociable from the birth and interactions of human societies, but is at best a secondary concern for scholars of international relations and globalization. Contemporary global studies are thus unable to account for the co-constitution of knowledge and politics at a macro-scale, and remain especially blind to the historical patterns of epistemic development that operate at the level of the species as a whole and have shaped its global political history in specific, path-dependent ways up to now.
ARTEFACT is the first project to pursue a knowledge-centered investigation of global politics. It is uniquely grounded in an anthropological approach that treats globalization and human knowledges beyond their modern manifestations, from the longue-durée perspective of our species’ social history. 'The global as artefact' is more than a metaphor. It reflects the premise that human collectives 'make' the political world not merely through ideas, language, or norms, but primordially through the material infrastructures, solutions, objects, practices, and skills they develop in response to evolving structural challenges.
ARTEFACT takes agriculture as an exemplary and especially timely case-study to illuminate the entangled global histories of knowledge and politics, analyzing and comparing four increasingly inclusive 'global political systems' of the Ancient, Medieval, Modern, and Contemporary eras and their associated agrarian socio-epistemic revolutions.
ARTEFACT ultimately aims to 1) develop an original theory of the global, 2) launch Global Knowledge Studies as a new cross-disciplinary domain of systematic empirical and theoretical study, and 3) push the respective boundaries of the anthropology of knowledge, global history, and international theory beyond the state-of-the-art and toward a holistic understanding that can illuminate how past trends of socio-epistemic evolution might shape future paths of global life.
Summary
Knowledge is an anthropological constant that is indissociable from the birth and interactions of human societies, but is at best a secondary concern for scholars of international relations and globalization. Contemporary global studies are thus unable to account for the co-constitution of knowledge and politics at a macro-scale, and remain especially blind to the historical patterns of epistemic development that operate at the level of the species as a whole and have shaped its global political history in specific, path-dependent ways up to now.
ARTEFACT is the first project to pursue a knowledge-centered investigation of global politics. It is uniquely grounded in an anthropological approach that treats globalization and human knowledges beyond their modern manifestations, from the longue-durée perspective of our species’ social history. 'The global as artefact' is more than a metaphor. It reflects the premise that human collectives 'make' the political world not merely through ideas, language, or norms, but primordially through the material infrastructures, solutions, objects, practices, and skills they develop in response to evolving structural challenges.
ARTEFACT takes agriculture as an exemplary and especially timely case-study to illuminate the entangled global histories of knowledge and politics, analyzing and comparing four increasingly inclusive 'global political systems' of the Ancient, Medieval, Modern, and Contemporary eras and their associated agrarian socio-epistemic revolutions.
ARTEFACT ultimately aims to 1) develop an original theory of the global, 2) launch Global Knowledge Studies as a new cross-disciplinary domain of systematic empirical and theoretical study, and 3) push the respective boundaries of the anthropology of knowledge, global history, and international theory beyond the state-of-the-art and toward a holistic understanding that can illuminate how past trends of socio-epistemic evolution might shape future paths of global life.
Max ERC Funding
1 428 165 €
Duration
Start date: 2017-09-01, End date: 2022-08-31
Project acronym ARYLATOR
Project New Catalytic Reactions and Exchange Pathways: Delivering Versatile and Reliable Arylation
Researcher (PI) Guy Charles Lloyd-Jones
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Advanced Grant (AdG), PE5, ERC-2013-ADG
Summary This proposal details the mechanism-based discovery of ground-breaking new catalyst systems for a broad range of arylation processes that will be of immediate and long-lasting utility to the pharmaceutical, agrochemical, and materials chemistry industries. These industries have become highly dependent on coupling technologies employing homogeneous late transition metal catalysis and this reliance will grow further, particularly if the substrate scope can be broadened, the economics, in terms of reagents and catalyst, made more favourable, the reliability at scale-up improved, and the generation of side-products, of particular importance for optical and electronic properties of materials, minimized or eliminated.
This proposal addresses these issues by conducting a detailed and comprehensive mechanistic investigation of direct arylation, so that a substantial expansion of the reaction scope can be achieved. At present, the regioselectivity can be very high, however catalyst turnover rates are moderate, and the arene is required to be in a fairly narrow window of activity. Specific aspects to be addressed in terms of mechanistic study are: catalyst speciation and pathways for deactivation; pathways for homocoupling; influence of anions and dummy ligands; protodemetalloidation pathways. Areas proposed for mechanism-informed development are: expansion of metalloid tolerance; expansion of arene scope; use of traceless activators and directors, new couplings via ligand exchange, the evolution of simpler / cheaper and more selective / active catalysts; expansion to oxidative double arylations (Ar-H + Ar’-H) with control, and without resort to super-stoichiometric bias.
The long-term legacy of these studies will be detailed insight for current and emerging systems, as well as readily extrapolated information for the design of new, more efficient catalyst systems in academia, and their scaleable application in industry
Summary
This proposal details the mechanism-based discovery of ground-breaking new catalyst systems for a broad range of arylation processes that will be of immediate and long-lasting utility to the pharmaceutical, agrochemical, and materials chemistry industries. These industries have become highly dependent on coupling technologies employing homogeneous late transition metal catalysis and this reliance will grow further, particularly if the substrate scope can be broadened, the economics, in terms of reagents and catalyst, made more favourable, the reliability at scale-up improved, and the generation of side-products, of particular importance for optical and electronic properties of materials, minimized or eliminated.
This proposal addresses these issues by conducting a detailed and comprehensive mechanistic investigation of direct arylation, so that a substantial expansion of the reaction scope can be achieved. At present, the regioselectivity can be very high, however catalyst turnover rates are moderate, and the arene is required to be in a fairly narrow window of activity. Specific aspects to be addressed in terms of mechanistic study are: catalyst speciation and pathways for deactivation; pathways for homocoupling; influence of anions and dummy ligands; protodemetalloidation pathways. Areas proposed for mechanism-informed development are: expansion of metalloid tolerance; expansion of arene scope; use of traceless activators and directors, new couplings via ligand exchange, the evolution of simpler / cheaper and more selective / active catalysts; expansion to oxidative double arylations (Ar-H + Ar’-H) with control, and without resort to super-stoichiometric bias.
The long-term legacy of these studies will be detailed insight for current and emerging systems, as well as readily extrapolated information for the design of new, more efficient catalyst systems in academia, and their scaleable application in industry
Max ERC Funding
2 114 223 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym ASA
Project Understanding Statehood through Architecture: a comparative study of Africa's state buildings
Researcher (PI) Julia Catherine GALLAGHER
Host Institution (HI) SCHOOL OF ORIENTAL AND AFRICAN STUDIES ROYAL CHARTER
Call Details Consolidator Grant (CoG), SH2, ERC-2017-COG
Summary The project will develop a new ethnography of statehood through architecture. It goes beyond conventional approaches to statehood, which describe states as an objectively existing set of tools used to run a country, and critical approaches that understand them as discursive constructs. Instead, this research understands statehood as a result of the relationship between functions and symbols, and will read it through an innovative new methodology, namely a study of state architecture.
The study will focus on state buildings in Africa. African statehood, uncertain and often ambiguous, in many cases profoundly shaped by colonial heritages and post-colonial relationships, is reflected in classical-colonial, modernist-nationalist and post-modern or vernacular styles of architecture. African state buildings reveal the complex interplay of ideas, activities and relationships that together constitute an often uncomfortable statehood. They symbolise the state, embodying and projecting ideas of it through their aesthetics; they enable its concrete functions and processes; and they reveal what citizens think about the state in the ways they describe and negotiate them.
The study is comparative, multi-layered and interdisciplinary. It focuses on seven countries (South Africa, Tanzania, DR Congo, Ethiopia, Ghana, Côte d’Ivoire and Guinea Bissau), exploring politics and statehood on domestic, regional and international levels, and drawing on theory and methods from political science, history, sociology, art and architecture theory. It employs innovative ethnographic methods, including the collection and display of photographs in interactive exhibitions staged in Africa to explore the ways citizens think about and use state buildings.
This project will provide an innovative reading of how African statehood is expressed and how it looks and feels to African citizens. In doing this, it will make a distinctive new contribution to understanding how statehood works everywhere.
Summary
The project will develop a new ethnography of statehood through architecture. It goes beyond conventional approaches to statehood, which describe states as an objectively existing set of tools used to run a country, and critical approaches that understand them as discursive constructs. Instead, this research understands statehood as a result of the relationship between functions and symbols, and will read it through an innovative new methodology, namely a study of state architecture.
The study will focus on state buildings in Africa. African statehood, uncertain and often ambiguous, in many cases profoundly shaped by colonial heritages and post-colonial relationships, is reflected in classical-colonial, modernist-nationalist and post-modern or vernacular styles of architecture. African state buildings reveal the complex interplay of ideas, activities and relationships that together constitute an often uncomfortable statehood. They symbolise the state, embodying and projecting ideas of it through their aesthetics; they enable its concrete functions and processes; and they reveal what citizens think about the state in the ways they describe and negotiate them.
The study is comparative, multi-layered and interdisciplinary. It focuses on seven countries (South Africa, Tanzania, DR Congo, Ethiopia, Ghana, Côte d’Ivoire and Guinea Bissau), exploring politics and statehood on domestic, regional and international levels, and drawing on theory and methods from political science, history, sociology, art and architecture theory. It employs innovative ethnographic methods, including the collection and display of photographs in interactive exhibitions staged in Africa to explore the ways citizens think about and use state buildings.
This project will provide an innovative reading of how African statehood is expressed and how it looks and feels to African citizens. In doing this, it will make a distinctive new contribution to understanding how statehood works everywhere.
Max ERC Funding
1 870 665 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym ASPIRE
Project Aqueous Supramolecular Polymers and Peptide Conjugates in Reversible Systems
Researcher (PI) Oren Alexander Scherman
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Starting Grant (StG), PE5, ERC-2009-StG
Summary Supramolecular polymers are of major interest in the field of self assembly with a promising outlook in areas of viscosity modification, compartmentalized architectures, bio-conjugates and drug-delivery applications. They are dynamic macromolecular materials prepared by simple mixing of relatively small components bearing complementary or self-complementary recognition motifs. A major limitation in the field, however, has been access to synthetic systems capable of undergoing self assembly in an aqueous environment. This research proposal develops well-defined, self-organizing macromolecular structures that will overcome this limitation by focusing on systems that rely on several non-covalent interactions occurring in concert rather than on single interactions alone. The envisioned supramolecular polymers and bio-conjugates are designed as dynamic water-soluble smart materials, whose architectures can be controlled and exhibit reversibility upon exposure to external stimuli such as electrochemical, temperature or pH changes. Molecular recognition events occurring between functional handles on both synthetic and bio-polymers will be investigated in order to control the formation of desired functional architectures through stoichiometrically controlled complexation. Preparation of synthetic core motifs to assemble discrete peptide aggregates such as the dimeric through hexameric oligomers of amyloid-beta(40/42) will lead to structural elucidation and insight into several peptide misfolding pathologies like Alzheimer's or Parkinson's disease.
Summary
Supramolecular polymers are of major interest in the field of self assembly with a promising outlook in areas of viscosity modification, compartmentalized architectures, bio-conjugates and drug-delivery applications. They are dynamic macromolecular materials prepared by simple mixing of relatively small components bearing complementary or self-complementary recognition motifs. A major limitation in the field, however, has been access to synthetic systems capable of undergoing self assembly in an aqueous environment. This research proposal develops well-defined, self-organizing macromolecular structures that will overcome this limitation by focusing on systems that rely on several non-covalent interactions occurring in concert rather than on single interactions alone. The envisioned supramolecular polymers and bio-conjugates are designed as dynamic water-soluble smart materials, whose architectures can be controlled and exhibit reversibility upon exposure to external stimuli such as electrochemical, temperature or pH changes. Molecular recognition events occurring between functional handles on both synthetic and bio-polymers will be investigated in order to control the formation of desired functional architectures through stoichiometrically controlled complexation. Preparation of synthetic core motifs to assemble discrete peptide aggregates such as the dimeric through hexameric oligomers of amyloid-beta(40/42) will lead to structural elucidation and insight into several peptide misfolding pathologies like Alzheimer's or Parkinson's disease.
Max ERC Funding
1 700 000 €
Duration
Start date: 2009-11-01, End date: 2015-10-31
Project acronym ASSIMILES
Project Advanced Spectroscopy and Spectrometry for Imaging Metabolism using Isotopically-Labeled Endogenous Substrates
Researcher (PI) Arnaud Comment
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Consolidator Grant (CoG), PE4, ERC-2015-CoG
Summary A technological revolution is currently taking place making it possible to noninvasively study metabolism in mammals (incl. humans) in vivo with unprecedented temporal and spatial resolution. Central to these developments is the phenomenon of hyperpolarization, which transiently enhances the magnetic resonance (MR) signals so much that real-time metabolic imaging and spectroscopy becomes possible. The first clinical translation of hyperpolarization MR technology has recently been demonstrated with prostate cancer patients.
I have played an active role in these exciting developments, through design and construction of hyperpolarization MR setups that are defining the cutting-edge for in vivo preclinical metabolic studies. However, important obstacles still exist for the technology to fulfill its enormous potential.
With this highly interdisciplinary proposal, I will overcome the principal drawbacks of current hyperpolarization technology, namely: 1) A limited time window for hyperpolarized MR detection; 2) The conventional use of potentially toxic polarizing agents; 3) The necessity to use supra-physiological doses of metabolic substrates to reach detectable MR signal
I will develop a novel hyperpolarization instrument making use of photoexcited compounds as polarizing agents to produce hyperpolarized solutions containing exclusively endogenous compounds. It will become possible to deliver hyperpolarized solutions in a quasi-continuous manner, permitting infusion of physiological doses and greatly increasing sensitivity. I will also use a complementary isotope imaging technique, the so-called CryoNanoSIMS (developed at my institution over the last year), which can image isotopic distributions in frozen tissue sections and reveal the localization of injected substrates and their metabolites with subcellular spatial resolution. Case studies will include liver and brain cancer mouse models. This work is pioneering and will create a new frontier in molecular imaging.
Summary
A technological revolution is currently taking place making it possible to noninvasively study metabolism in mammals (incl. humans) in vivo with unprecedented temporal and spatial resolution. Central to these developments is the phenomenon of hyperpolarization, which transiently enhances the magnetic resonance (MR) signals so much that real-time metabolic imaging and spectroscopy becomes possible. The first clinical translation of hyperpolarization MR technology has recently been demonstrated with prostate cancer patients.
I have played an active role in these exciting developments, through design and construction of hyperpolarization MR setups that are defining the cutting-edge for in vivo preclinical metabolic studies. However, important obstacles still exist for the technology to fulfill its enormous potential.
With this highly interdisciplinary proposal, I will overcome the principal drawbacks of current hyperpolarization technology, namely: 1) A limited time window for hyperpolarized MR detection; 2) The conventional use of potentially toxic polarizing agents; 3) The necessity to use supra-physiological doses of metabolic substrates to reach detectable MR signal
I will develop a novel hyperpolarization instrument making use of photoexcited compounds as polarizing agents to produce hyperpolarized solutions containing exclusively endogenous compounds. It will become possible to deliver hyperpolarized solutions in a quasi-continuous manner, permitting infusion of physiological doses and greatly increasing sensitivity. I will also use a complementary isotope imaging technique, the so-called CryoNanoSIMS (developed at my institution over the last year), which can image isotopic distributions in frozen tissue sections and reveal the localization of injected substrates and their metabolites with subcellular spatial resolution. Case studies will include liver and brain cancer mouse models. This work is pioneering and will create a new frontier in molecular imaging.
Max ERC Funding
2 199 146 €
Duration
Start date: 2016-09-01, End date: 2021-08-31
Project acronym ATMEN
Project Atomic precision materials engineering
Researcher (PI) Toma SUSI
Host Institution (HI) UNIVERSITAT WIEN
Call Details Starting Grant (StG), PE5, ERC-2017-STG
Summary Despite more than fifty years of scientific progress since Richard Feynman's 1959 vision for nanotechnology, there is only one way to manipulate individual atoms in materials: scanning tunneling microscopy. Since the late 1980s, its atomically sharp tip has been used to move atoms over clean metal surfaces held at cryogenic temperatures. Scanning transmission electron microscopy, on the other hand, has been able to resolve atoms only more recently by focusing the electron beam with sub-atomic precision. This is especially useful in the two-dimensional form of hexagonally bonded carbon called graphene, which has superb electronic and mechanical properties. Several ways to further engineer those have been proposed, including by doping the structure with substitutional heteroatoms such as boron, nitrogen, phosphorus and silicon. My recent discovery that the scattering of the energetic imaging electrons can cause a silicon impurity to move through the graphene lattice has revealed a potential for atomically precise manipulation using the Ångström-sized electron probe. To develop this into a practical technique, improvements in the description of beam-induced displacements, advances in heteroatom implantation, and a concerted effort towards the automation of manipulations are required. My project tackles these in a multidisciplinary effort combining innovative computational techniques with pioneering experiments in an instrument where a low-energy ion implantation chamber is directly connected to an advanced electron microscope. To demonstrate the power of the method, I will prototype an atomic memory with an unprecedented memory density, and create heteroatom quantum corrals optimized for their plasmonic properties. The capability for atom-scale engineering of covalent materials opens a new vista for nanotechnology, pushing back the boundaries of the possible and allowing a plethora of materials science questions to be studied at the ultimate level of control.
Summary
Despite more than fifty years of scientific progress since Richard Feynman's 1959 vision for nanotechnology, there is only one way to manipulate individual atoms in materials: scanning tunneling microscopy. Since the late 1980s, its atomically sharp tip has been used to move atoms over clean metal surfaces held at cryogenic temperatures. Scanning transmission electron microscopy, on the other hand, has been able to resolve atoms only more recently by focusing the electron beam with sub-atomic precision. This is especially useful in the two-dimensional form of hexagonally bonded carbon called graphene, which has superb electronic and mechanical properties. Several ways to further engineer those have been proposed, including by doping the structure with substitutional heteroatoms such as boron, nitrogen, phosphorus and silicon. My recent discovery that the scattering of the energetic imaging electrons can cause a silicon impurity to move through the graphene lattice has revealed a potential for atomically precise manipulation using the Ångström-sized electron probe. To develop this into a practical technique, improvements in the description of beam-induced displacements, advances in heteroatom implantation, and a concerted effort towards the automation of manipulations are required. My project tackles these in a multidisciplinary effort combining innovative computational techniques with pioneering experiments in an instrument where a low-energy ion implantation chamber is directly connected to an advanced electron microscope. To demonstrate the power of the method, I will prototype an atomic memory with an unprecedented memory density, and create heteroatom quantum corrals optimized for their plasmonic properties. The capability for atom-scale engineering of covalent materials opens a new vista for nanotechnology, pushing back the boundaries of the possible and allowing a plethora of materials science questions to be studied at the ultimate level of control.
Max ERC Funding
1 497 202 €
Duration
Start date: 2017-10-01, End date: 2022-09-30
Project acronym AtoFun
Project Atomic Scale Defects: Structure and Function
Researcher (PI) Felix HOFMANN
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), PE5, ERC-2016-STG
Summary Atomic scale defects play a key role in determining the behaviour of all crystalline materials, profoundly modifying mechanical, thermal and electrical properties. Many current technological applications make do with phenomenological descriptions of these effects; yet myriad intriguing questions about the fundamental link between defect structure and material function remain.
Transmission electron microscopy revolutionised the study of atomic scale defects by enabling their direct imaging. The novel coherent X-ray diffraction techniques developed in this project promise a similar advancement, making it possible to probe the strain fields that govern defect interactions in 3D with high spatial resolution (<10 nm). They will allow us to clarify the effect of impurities and retained gas on dislocation strain fields, shedding light on opportunities to engineer dislocation properties. The exceptional strain sensitivity of coherent diffraction will enable us to explore the fundamental mechanisms governing the behaviour of ion-implantation-induced point defects that are invisible to TEM. While we concentrate on dislocations and point defects, the new techniques will apply to all crystalline materials where defects are important. Our characterisation of defect structure will be combined with laser transient grating measurements of thermal transport changes due to specific defect populations. This unique multifaceted perspective of defect behaviour will transform our ability to devise modelling approaches linking defect structure to material function.
Our proof-of-concept results highlight the feasibility of this ambitious research project. It opens up a vast range of exciting possibilities to gain a deep, fundamental understanding of atomic scale defects and their effect on material function. This is an essential prerequisite for exploiting and engineering defects to enhance material properties.
Summary
Atomic scale defects play a key role in determining the behaviour of all crystalline materials, profoundly modifying mechanical, thermal and electrical properties. Many current technological applications make do with phenomenological descriptions of these effects; yet myriad intriguing questions about the fundamental link between defect structure and material function remain.
Transmission electron microscopy revolutionised the study of atomic scale defects by enabling their direct imaging. The novel coherent X-ray diffraction techniques developed in this project promise a similar advancement, making it possible to probe the strain fields that govern defect interactions in 3D with high spatial resolution (<10 nm). They will allow us to clarify the effect of impurities and retained gas on dislocation strain fields, shedding light on opportunities to engineer dislocation properties. The exceptional strain sensitivity of coherent diffraction will enable us to explore the fundamental mechanisms governing the behaviour of ion-implantation-induced point defects that are invisible to TEM. While we concentrate on dislocations and point defects, the new techniques will apply to all crystalline materials where defects are important. Our characterisation of defect structure will be combined with laser transient grating measurements of thermal transport changes due to specific defect populations. This unique multifaceted perspective of defect behaviour will transform our ability to devise modelling approaches linking defect structure to material function.
Our proof-of-concept results highlight the feasibility of this ambitious research project. It opens up a vast range of exciting possibilities to gain a deep, fundamental understanding of atomic scale defects and their effect on material function. This is an essential prerequisite for exploiting and engineering defects to enhance material properties.
Max ERC Funding
1 610 231 €
Duration
Start date: 2017-03-01, End date: 2022-02-28
Project acronym Autocat
Project Autocatalysis: A bottom-up approach to understanding the origins of life
Researcher (PI) Stephen Patrick Fletcher
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Consolidator Grant (CoG), PE5, ERC-2015-CoG
Summary "The origin of life is not well understood, and is one of the great remaining questions in science. Autocatalytic chemical reactions have been extensively studied with the aim of providing insight into the principles underlying living systems. In biology, organisms can be thought of as imperfect self-replicators, which produce closely related species, allowing for selection and evolution. Autocatalysis is also an important part of many other biological processes.
This project aims to develop new autocatalytic reactions where two simple chemical building blocks come together to give a more complex product, and then the product aggregates to give primitive cell-like structures or "protocells" such as micelles or vesicles. The protocells allow the starting materials to mix more efficiently, speeding up the reaction in time and giving rise to complex behaviour of the protocells. These reactions will serve as models that I hope will contribute to understanding how cell-like systems can emerge from simpler chemicals and be relevant to how life started on earth.
This project will give the opportunity to study chemical systems that may be able to evolve in time, allow development of useful chemical models of important biological processes, and provide ‘bottom-up’ approaches to synthetic biology. This research will potential allow the study evolution in a new ways, develop technology useful to a number of scientific fields, and potentially shed light on the processes that allowed chemistry to become biology on the primitive Earth."
Summary
"The origin of life is not well understood, and is one of the great remaining questions in science. Autocatalytic chemical reactions have been extensively studied with the aim of providing insight into the principles underlying living systems. In biology, organisms can be thought of as imperfect self-replicators, which produce closely related species, allowing for selection and evolution. Autocatalysis is also an important part of many other biological processes.
This project aims to develop new autocatalytic reactions where two simple chemical building blocks come together to give a more complex product, and then the product aggregates to give primitive cell-like structures or "protocells" such as micelles or vesicles. The protocells allow the starting materials to mix more efficiently, speeding up the reaction in time and giving rise to complex behaviour of the protocells. These reactions will serve as models that I hope will contribute to understanding how cell-like systems can emerge from simpler chemicals and be relevant to how life started on earth.
This project will give the opportunity to study chemical systems that may be able to evolve in time, allow development of useful chemical models of important biological processes, and provide ‘bottom-up’ approaches to synthetic biology. This research will potential allow the study evolution in a new ways, develop technology useful to a number of scientific fields, and potentially shed light on the processes that allowed chemistry to become biology on the primitive Earth."
Max ERC Funding
2 278 073 €
Duration
Start date: 2016-05-01, End date: 2021-04-30
Project acronym BANK-LASH
Project Banks, Popular Backlash, and the Post-Crisis Politics of Financial Regulation
Researcher (PI) Pepper CULPEPPER
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Advanced Grant (AdG), SH2, ERC-2017-ADG
Summary Driven by public outrage at bank bailouts during the financial crisis, many governments have since then tried to rewrite the rules governing finance. Yet the anger provoked by the bailouts has not subsided. In Europe and in North America, citizen fury against bankers continues to structure battles over financial regulation. It also affects broader perceptions of fairness in the political system and feeds anti-elite populism. Scholars of political economy have chronicled the clashes between states and large banks, and scholars of political behaviour have noted the failings of governments to respond to the will of democratic majorities. No one has explored the feedback loops between policies regulating banks, the public anger towards banking elites, and media discussions of finance. BANK-LASH fills this gap, using a cutting-edge, high-risk research design comprising three work packages to link policy outcomes with public opinion and media coverage. BANK-LASH 1will collect the first cross-nationally comparable data on public attitudes towards finance, including a series of innovative survey experiments that assess how different media frames affect emotions and preferences. BANK-LASH 2 will use supervised machine learning to measure the overall media environment of these countries for the last decade, assessing how much different national media systems discuss finance and how different national media systems frame the discussion of banking regulation. BANK-LASH 3 links the micro-level study of attitudes and macro-level media coverage with episodes of policy intervention in each country in order to determine when democracies have imposed significant new regulation on their banks. By harnessing these different intellectual tools within a single study, BANK-LASH brings together the concerns of political economy, behavioral research and policy studies to untangle the relationship between banks, public policy, and anti-elite sentiment in the wake of the financial crisis.
Summary
Driven by public outrage at bank bailouts during the financial crisis, many governments have since then tried to rewrite the rules governing finance. Yet the anger provoked by the bailouts has not subsided. In Europe and in North America, citizen fury against bankers continues to structure battles over financial regulation. It also affects broader perceptions of fairness in the political system and feeds anti-elite populism. Scholars of political economy have chronicled the clashes between states and large banks, and scholars of political behaviour have noted the failings of governments to respond to the will of democratic majorities. No one has explored the feedback loops between policies regulating banks, the public anger towards banking elites, and media discussions of finance. BANK-LASH fills this gap, using a cutting-edge, high-risk research design comprising three work packages to link policy outcomes with public opinion and media coverage. BANK-LASH 1will collect the first cross-nationally comparable data on public attitudes towards finance, including a series of innovative survey experiments that assess how different media frames affect emotions and preferences. BANK-LASH 2 will use supervised machine learning to measure the overall media environment of these countries for the last decade, assessing how much different national media systems discuss finance and how different national media systems frame the discussion of banking regulation. BANK-LASH 3 links the micro-level study of attitudes and macro-level media coverage with episodes of policy intervention in each country in order to determine when democracies have imposed significant new regulation on their banks. By harnessing these different intellectual tools within a single study, BANK-LASH brings together the concerns of political economy, behavioral research and policy studies to untangle the relationship between banks, public policy, and anti-elite sentiment in the wake of the financial crisis.
Max ERC Funding
2 454 198 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym BATNMR
Project Development and Application of New NMR Methods for Studying Interphases and Interfaces in Batteries
Researcher (PI) Clare GREY
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Advanced Grant (AdG), PE4, ERC-2018-ADG
Summary The development of longer lasting, higher energy density and cheaper rechargeable batteries represents one of the major technological challenges of our society, batteries representing the limiting components in the shift from gasoline-powered to electric vehicles. They are also required to enable the use of more (typically intermittent) renewable energy, to balance demand with generation. This proposal seeks to develop and apply new NMR metrologies to determine the structure and dynamics of the multiple electrode-electrolyte interfaces and interphases that are present in these batteries, and how they evolve during battery cycling. New dynamic nuclear polarization (DNP) techniques will be exploited to extract structural information about the interface between the battery electrode and the passivating layers that grow on the electrode materials (the solid electrolyte interphase, SEI) and that are inherent to the stability of the batteries. The role of the SEI (and ceramic interfaces) in controlling lithium metal dendrite growth will be determined in liquid based and all solid state batteries.
New DNP approaches will be developed that are compatible with the heterogeneous and reactive species that are present in conventional, all-solid state, Li-air and redox flow batteries. Method development will run in parallel with the use of DNP approaches to determine the structures of the various battery interfaces and interphases, testing the stability of conventional biradicals in these harsh oxidizing and reducing conditions, modifying the experimental approaches where appropriate. The final result will be a significantly improved understanding of the structures of these phases and how they evolve on cycling, coupled with strategies for designing improved SEI structures. The nature of the interface between a lithium metal dendrite and ceramic composite will be determined, providing much needed insight into how these (unwanted) dendrites grow in all solid state batteries. DNP approaches coupled with electron spin resonance will be use, where possible in situ, to determine the reaction mechanisms of organic molecules such as quinones in organic-based redox flow batteries in order to help prevent degradation of the electrochemically active species.
This proposal involves NMR method development specifically designed to explore a variety of battery chemistries. Thus, this proposal is interdisciplinary, containing both a strong emphasis on materials characterization, electrochemistry and electronic structures of materials, interfaces and nanoparticles, and on analytical and physical chemistry. Some of the methodology will be applicable to other materials and systems including (for example) other electrochemical technologies such as fuel cells and solar fuels and the study of catalysts (to probe surface structure).
Summary
The development of longer lasting, higher energy density and cheaper rechargeable batteries represents one of the major technological challenges of our society, batteries representing the limiting components in the shift from gasoline-powered to electric vehicles. They are also required to enable the use of more (typically intermittent) renewable energy, to balance demand with generation. This proposal seeks to develop and apply new NMR metrologies to determine the structure and dynamics of the multiple electrode-electrolyte interfaces and interphases that are present in these batteries, and how they evolve during battery cycling. New dynamic nuclear polarization (DNP) techniques will be exploited to extract structural information about the interface between the battery electrode and the passivating layers that grow on the electrode materials (the solid electrolyte interphase, SEI) and that are inherent to the stability of the batteries. The role of the SEI (and ceramic interfaces) in controlling lithium metal dendrite growth will be determined in liquid based and all solid state batteries.
New DNP approaches will be developed that are compatible with the heterogeneous and reactive species that are present in conventional, all-solid state, Li-air and redox flow batteries. Method development will run in parallel with the use of DNP approaches to determine the structures of the various battery interfaces and interphases, testing the stability of conventional biradicals in these harsh oxidizing and reducing conditions, modifying the experimental approaches where appropriate. The final result will be a significantly improved understanding of the structures of these phases and how they evolve on cycling, coupled with strategies for designing improved SEI structures. The nature of the interface between a lithium metal dendrite and ceramic composite will be determined, providing much needed insight into how these (unwanted) dendrites grow in all solid state batteries. DNP approaches coupled with electron spin resonance will be use, where possible in situ, to determine the reaction mechanisms of organic molecules such as quinones in organic-based redox flow batteries in order to help prevent degradation of the electrochemically active species.
This proposal involves NMR method development specifically designed to explore a variety of battery chemistries. Thus, this proposal is interdisciplinary, containing both a strong emphasis on materials characterization, electrochemistry and electronic structures of materials, interfaces and nanoparticles, and on analytical and physical chemistry. Some of the methodology will be applicable to other materials and systems including (for example) other electrochemical technologies such as fuel cells and solar fuels and the study of catalysts (to probe surface structure).
Max ERC Funding
3 498 219 €
Duration
Start date: 2019-10-01, End date: 2024-09-30
Project acronym BBSG
Project Bosnian Bones, Spanish Ghosts: 'Transitional Justice' and the Legal Shaping of Memory after Two Modern Conflicts
Researcher (PI) Sarah Lynn Wastell (Born Haller)
Host Institution (HI) GOLDSMITHS' COLLEGE
Call Details Starting Grant (StG), SH2, ERC-2009-StG
Summary The proposed research entails an ethnographic study of two contemporary cases of post-conflict reconciliation: one, the Bosnian case, where international intervention ended conflict in a stalemate and went on to instigate a decade-long process of transition; and the other, the Spanish case, where a nationally-contrived pact of silence introduced an overnight transition after Franco's death a pact now being broken nearly seventy years after the country's civil war concluded. Both societies witnessed massive violations of international humanitarian law. Both societies are presently exhuming, identifying and re-burying their dead. But their trajectories of transitional justice could not have been more different. This project will investigate how Law shapes cultural memories of wartime atrocity in these contrasting scenarios. How do criminal prosecutions, constitutional reforms, and international rights mechanisms, provide or obfuscate the scales into which histories of violent conflict are framed? Does the systematic re-structuring of legislative and judicial infrastructure stifle recognition of past abuses or does it create the conditions through which such pasts can be confronted? How does Law shape or inflect the cultural politics of memory and memorialisation? And most importantly, how should legal activity be weighted, prioritised and sequenced with other, extra-legal components of peace-building initiatives? The ultimate goal of this project will be to mobilise the findings from the two field-sites to suggest a more nuanced assessment of Law s place in transitional justice. Arguing that disparate historical, cultural and legal contexts require equally distinct approaches towards social healing, the research aims to produce a Post-Conflict Action Framework an architecture of questions and concerns, which, once answered, would point towards context-specific designs for transitional justice programmes in the future.
Summary
The proposed research entails an ethnographic study of two contemporary cases of post-conflict reconciliation: one, the Bosnian case, where international intervention ended conflict in a stalemate and went on to instigate a decade-long process of transition; and the other, the Spanish case, where a nationally-contrived pact of silence introduced an overnight transition after Franco's death a pact now being broken nearly seventy years after the country's civil war concluded. Both societies witnessed massive violations of international humanitarian law. Both societies are presently exhuming, identifying and re-burying their dead. But their trajectories of transitional justice could not have been more different. This project will investigate how Law shapes cultural memories of wartime atrocity in these contrasting scenarios. How do criminal prosecutions, constitutional reforms, and international rights mechanisms, provide or obfuscate the scales into which histories of violent conflict are framed? Does the systematic re-structuring of legislative and judicial infrastructure stifle recognition of past abuses or does it create the conditions through which such pasts can be confronted? How does Law shape or inflect the cultural politics of memory and memorialisation? And most importantly, how should legal activity be weighted, prioritised and sequenced with other, extra-legal components of peace-building initiatives? The ultimate goal of this project will be to mobilise the findings from the two field-sites to suggest a more nuanced assessment of Law s place in transitional justice. Arguing that disparate historical, cultural and legal contexts require equally distinct approaches towards social healing, the research aims to produce a Post-Conflict Action Framework an architecture of questions and concerns, which, once answered, would point towards context-specific designs for transitional justice programmes in the future.
Max ERC Funding
1 420 000 €
Duration
Start date: 2009-09-01, End date: 2013-08-31
Project acronym BENELEX
Project Benefit-sharing for an equitable transition to the green economy - the role of law
Researcher (PI) Elisa Morgera
Host Institution (HI) UNIVERSITY OF STRATHCLYDE
Call Details Starting Grant (StG), SH2, ERC-2013-StG
Summary Can benefit-sharing address the equity deficit within the green economy? This project aims to investigate benefit-sharing as an under-theorised and little-implemented regulatory approach to the equity concerns (disregard for the special circumstances of developing countries and of indigenous peoples and local communities) in transitioning to the green economy.
Although benefit-sharing is increasingly deployed in a variety of international environmental agreements and also in human rights and corporate accountability instruments, no comprehensive account exists of its conceptual and practical relevance to equitably address global environmental challenges. This project will be the first systematic evaluation of the conceptualisations and operationalisations of benefit-sharing as a tool for equitable change through the allocation among different stakeholders of economic and also socio-cultural and environmental advantages arising from natural resource use.
The project will combine a comparative study of international law with empirical legal research, and include an inter-disciplinary study integrating political sociology in a legal enquiry on the role of “biocultural community protocols” that articulate and implement benefit-sharing at the intersection of international, transnational, national and indigenous communities’ customary law (global environmental law).
The project aims to: 1. develop a comprehensive understanding of benefit-sharing in international law; 2. clarify whether and how benefit-sharing supports equity and the protection of human rights across key sectors of international environmental regulation (biodiversity, climate change, oceans, food and agriculture) that are seen as inter-related in the transition to the green economy; 3. understand the development of benefit-sharing in the context of global environmental law; and
4. clarify the role of transnational legal advisors (NGOs and bilateral cooperation partners) in the green economy.
Summary
Can benefit-sharing address the equity deficit within the green economy? This project aims to investigate benefit-sharing as an under-theorised and little-implemented regulatory approach to the equity concerns (disregard for the special circumstances of developing countries and of indigenous peoples and local communities) in transitioning to the green economy.
Although benefit-sharing is increasingly deployed in a variety of international environmental agreements and also in human rights and corporate accountability instruments, no comprehensive account exists of its conceptual and practical relevance to equitably address global environmental challenges. This project will be the first systematic evaluation of the conceptualisations and operationalisations of benefit-sharing as a tool for equitable change through the allocation among different stakeholders of economic and also socio-cultural and environmental advantages arising from natural resource use.
The project will combine a comparative study of international law with empirical legal research, and include an inter-disciplinary study integrating political sociology in a legal enquiry on the role of “biocultural community protocols” that articulate and implement benefit-sharing at the intersection of international, transnational, national and indigenous communities’ customary law (global environmental law).
The project aims to: 1. develop a comprehensive understanding of benefit-sharing in international law; 2. clarify whether and how benefit-sharing supports equity and the protection of human rights across key sectors of international environmental regulation (biodiversity, climate change, oceans, food and agriculture) that are seen as inter-related in the transition to the green economy; 3. understand the development of benefit-sharing in the context of global environmental law; and
4. clarify the role of transnational legal advisors (NGOs and bilateral cooperation partners) in the green economy.
Max ERC Funding
1 481 708 €
Duration
Start date: 2013-11-01, End date: 2018-10-31
Project acronym BIO-H-BORROW
Project Biocatalytic Amine Synthesis via Hydrogen Borrowing
Researcher (PI) Nicholas TURNER
Host Institution (HI) THE UNIVERSITY OF MANCHESTER
Call Details Advanced Grant (AdG), PE5, ERC-2016-ADG
Summary Amine containing compounds are ubiquitous in everyday life and find applications ranging from polymers to pharmaceuticals. The vast majority of amines are synthetic and manufactured on large scale which creates waste as well as requiring high temperatures and pressures. The increasing availability of biocatalysts, together with an understanding of how they can be used in organic synthesis (biocatalytic retrosynthesis), has stimulated chemists to consider new ways of making target molecules. In this context, the iterative construction of C-N bonds via biocatalytic hydrogen borrowing represents a powerful and unexplored way to synthesise a wide range of target amine molecules in an efficient manner. Hydrogen borrowing involves telescoping redox neutral reactions together using only catalytic amounts of hydrogen.
In this project we will engineer the three key target biocatalysts (reductive aminase, amine dehydrogenase, alcohol dehydrogenase) required for biocatalytic hydrogen borrowing such that they possess the required regio-, chemo- and stereo-selectivity for practical application. Recently discovered reductive aminases (RedAms) and amine dehydrogenases (AmDHs) will be engineered for enantioselective coupling of alcohols (1o, 2o) with ammonia/amines (1o, 2o, 3o) under redox neutral conditions. Alcohol dehydrogenases will be engineered for low enantioselectivity. Hydrogen borrowing requires mutually compatible cofactors shared by two enzymes and in some cases will require redesign of cofactor specificity. Thereafter we shall develop conditions for the combined use of these biocatalysts under hydrogen borrowing conditions (catalytic NADH, NADPH), to enable the conversion of simple and sustainable feedstocks (alcohols) into amines using ammonia as the nitrogen source.
The main deliverables of BIO-H-BORROW will be a set of novel engineered biocatalysts together with redox neutral cascades for the synthesis of amine products from inexpensive and renewable precursors.
Summary
Amine containing compounds are ubiquitous in everyday life and find applications ranging from polymers to pharmaceuticals. The vast majority of amines are synthetic and manufactured on large scale which creates waste as well as requiring high temperatures and pressures. The increasing availability of biocatalysts, together with an understanding of how they can be used in organic synthesis (biocatalytic retrosynthesis), has stimulated chemists to consider new ways of making target molecules. In this context, the iterative construction of C-N bonds via biocatalytic hydrogen borrowing represents a powerful and unexplored way to synthesise a wide range of target amine molecules in an efficient manner. Hydrogen borrowing involves telescoping redox neutral reactions together using only catalytic amounts of hydrogen.
In this project we will engineer the three key target biocatalysts (reductive aminase, amine dehydrogenase, alcohol dehydrogenase) required for biocatalytic hydrogen borrowing such that they possess the required regio-, chemo- and stereo-selectivity for practical application. Recently discovered reductive aminases (RedAms) and amine dehydrogenases (AmDHs) will be engineered for enantioselective coupling of alcohols (1o, 2o) with ammonia/amines (1o, 2o, 3o) under redox neutral conditions. Alcohol dehydrogenases will be engineered for low enantioselectivity. Hydrogen borrowing requires mutually compatible cofactors shared by two enzymes and in some cases will require redesign of cofactor specificity. Thereafter we shall develop conditions for the combined use of these biocatalysts under hydrogen borrowing conditions (catalytic NADH, NADPH), to enable the conversion of simple and sustainable feedstocks (alcohols) into amines using ammonia as the nitrogen source.
The main deliverables of BIO-H-BORROW will be a set of novel engineered biocatalysts together with redox neutral cascades for the synthesis of amine products from inexpensive and renewable precursors.
Max ERC Funding
2 337 548 €
Duration
Start date: 2017-06-01, End date: 2022-05-31
Project acronym BiocatSusChem
Project Biocatalysis for Sustainable Chemistry – Understanding Oxidation/Reduction of Small Molecules by Redox Metalloenzymes via a Suite of Steady State and Transient Infrared Electrochemical Methods
Researcher (PI) Kylie VINCENT
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Consolidator Grant (CoG), PE4, ERC-2018-COG
Summary Many significant global challenges in catalysis for energy and sustainable chemistry have already been solved in nature. Metalloenzymes within microorganisms catalyse the transformation of carbon dioxide into simple carbon building blocks or fuels, the reduction of dinitrogen to ammonia under ambient conditions and the production and utilisation of dihydrogen. Catalytic sites for these reactions are necessarily based on metals that are abundant in the environment, including iron, nickel and molybdenum. However, attempts to generate biomimetic catalysts have largely failed to reproduce the high activity, stability and selectivity of enzymes. Proton and electron transfer and substrate binding are all finely choreographed, and we do not yet understand how this is achieved. This project develops a suite of new experimental infrared (IR) spectroscopy tools to probe and understand mechanisms of redox metalloenzymes in situ during electrochemically-controlled steady state turnover, and during electron-transfer-triggered transient studies. The ability of IR spectroscopy to report on the nature and strength of chemical bonds makes it ideally suited to follow the activation and transformation of small molecule reactants at metalloenzyme catalytic sites, binding of inhibitors, and protonation of specific sites. By extending to the far-IR, or introducing mid-IR-active probe amino acids, redox and structural changes in biological electron relay chains also become accessible. Taking as models the enzymes nitrogenase, hydrogenase, carbon monoxide dehydrogenase and formate dehydrogenase, the project sets out to establish a unified understanding of central concepts in small molecule activation in biology. It will reveal precise ways in which chemical events are coordinated inside complex multicentre metalloenzymes, propelling a new generation of bio-inspired catalysts and uncovering new chemistry of enzymes.
Summary
Many significant global challenges in catalysis for energy and sustainable chemistry have already been solved in nature. Metalloenzymes within microorganisms catalyse the transformation of carbon dioxide into simple carbon building blocks or fuels, the reduction of dinitrogen to ammonia under ambient conditions and the production and utilisation of dihydrogen. Catalytic sites for these reactions are necessarily based on metals that are abundant in the environment, including iron, nickel and molybdenum. However, attempts to generate biomimetic catalysts have largely failed to reproduce the high activity, stability and selectivity of enzymes. Proton and electron transfer and substrate binding are all finely choreographed, and we do not yet understand how this is achieved. This project develops a suite of new experimental infrared (IR) spectroscopy tools to probe and understand mechanisms of redox metalloenzymes in situ during electrochemically-controlled steady state turnover, and during electron-transfer-triggered transient studies. The ability of IR spectroscopy to report on the nature and strength of chemical bonds makes it ideally suited to follow the activation and transformation of small molecule reactants at metalloenzyme catalytic sites, binding of inhibitors, and protonation of specific sites. By extending to the far-IR, or introducing mid-IR-active probe amino acids, redox and structural changes in biological electron relay chains also become accessible. Taking as models the enzymes nitrogenase, hydrogenase, carbon monoxide dehydrogenase and formate dehydrogenase, the project sets out to establish a unified understanding of central concepts in small molecule activation in biology. It will reveal precise ways in which chemical events are coordinated inside complex multicentre metalloenzymes, propelling a new generation of bio-inspired catalysts and uncovering new chemistry of enzymes.
Max ERC Funding
1 997 286 €
Duration
Start date: 2019-03-01, End date: 2024-02-29
Project acronym BioDisOrder
Project Order and Disorder at the Surface of Biological Membranes.
Researcher (PI) Alfonso DE SIMONE
Host Institution (HI) IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Call Details Consolidator Grant (CoG), PE4, ERC-2018-COG
Summary Heterogeneous biomolecular mechanisms at the surface of cellular membranes are often fundamental to generate function and dysfunction in living systems. These processes are governed by transient and dynamical macromolecular interactions that pose tremendous challenges to current analytical tools, as the majority of these methods perform best in the study of well-defined and poorly dynamical systems. This proposal aims at a radical innovation in the characterisation of complex processes that are dominated by structural order and disorder, including those occurring at the surface of biological membranes such as cellular signalling, the assembly of molecular machinery, or the regulation vesicular trafficking.
I outline a programme to realise a vision where the combination of experiments and theory can delineate a new analytical platform to study complex biochemical mechanisms at a multiscale level, and to elucidate their role in physiological and pathological contexts. To achieve this ambitious goal, my research team will develop tools based on the combination of nuclear magnetic resonance (NMR) spectroscopy and molecular simulations, which will enable probing the structure, dynamics, thermodynamics and kinetics of complex protein-protein and protein-membrane interactions occurring at the surface of cellular membranes. The ability to advance both the experimental and theoretical sides, and their combination, is fundamental to define the next generation of methods to achieve our transformative aims. We will provide evidence of the innovative nature of the proposed multiscale approach by addressing some of the great questions in neuroscience and elucidate the details of how functional and aberrant biological complexity is achieved via the fine tuning between structural order and disorder at the neuronal synapse.
Summary
Heterogeneous biomolecular mechanisms at the surface of cellular membranes are often fundamental to generate function and dysfunction in living systems. These processes are governed by transient and dynamical macromolecular interactions that pose tremendous challenges to current analytical tools, as the majority of these methods perform best in the study of well-defined and poorly dynamical systems. This proposal aims at a radical innovation in the characterisation of complex processes that are dominated by structural order and disorder, including those occurring at the surface of biological membranes such as cellular signalling, the assembly of molecular machinery, or the regulation vesicular trafficking.
I outline a programme to realise a vision where the combination of experiments and theory can delineate a new analytical platform to study complex biochemical mechanisms at a multiscale level, and to elucidate their role in physiological and pathological contexts. To achieve this ambitious goal, my research team will develop tools based on the combination of nuclear magnetic resonance (NMR) spectroscopy and molecular simulations, which will enable probing the structure, dynamics, thermodynamics and kinetics of complex protein-protein and protein-membrane interactions occurring at the surface of cellular membranes. The ability to advance both the experimental and theoretical sides, and their combination, is fundamental to define the next generation of methods to achieve our transformative aims. We will provide evidence of the innovative nature of the proposed multiscale approach by addressing some of the great questions in neuroscience and elucidate the details of how functional and aberrant biological complexity is achieved via the fine tuning between structural order and disorder at the neuronal synapse.
Max ERC Funding
1 999 945 €
Duration
Start date: 2019-06-01, End date: 2024-05-31
Project acronym BIOINCMED
Project Bioinorganic Chemistry for the Design of New Medicines
Researcher (PI) Peter John Sadler
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Advanced Grant (AdG), PE5, ERC-2009-AdG
Summary Bioinorganic chemistry is a rapidly expanding area of research, but the potential for the therapeutic application of metal complexes is highly underdeveloped. The basic principles required to guide the development of metal-containing therapeutic agents are lacking, despite the unique therapeutic opportunities which they offer. It is the goal of the proposed research to establish basic principles of medicinal coordination chemistry of metals that will allow the rational screening of future metallopharmaceuticals. We propose to utilize the power of inorganic chemistry to provide new knowledge of and new approaches for intervention in biological systems. This will be based on improved understanding of reactions of metal complexes under physiological conditions, on improving the specificity of their interactions, and gaining control over the potential toxicity of synthetic metal complexes. The research programme is highly interdisciplinary involving chemistry, physics, biology and pharmacology, with potential for the discovery of truly novel medicines, especially for the treatment of diseases and conditions which are currently intractable, such as cancer. The challenging and ambitious goals of the present work involve transition metal complexes with novel chemical and biochemical mechanisms of action. They will contain novel features which allow them (i) to be selectively activated by light in cells, or (ii) to be activated by a structural transition, or (ii) exhibit catalytic activity in cells. This ground-breaking research potentially has a very high impact and is based on recent discoveries in the applicant s laboratory. A feature of the programme is the use of state-of-the-art-and-beyond methodology to advance knowledge of medicinal metal coordination chemistry.
Summary
Bioinorganic chemistry is a rapidly expanding area of research, but the potential for the therapeutic application of metal complexes is highly underdeveloped. The basic principles required to guide the development of metal-containing therapeutic agents are lacking, despite the unique therapeutic opportunities which they offer. It is the goal of the proposed research to establish basic principles of medicinal coordination chemistry of metals that will allow the rational screening of future metallopharmaceuticals. We propose to utilize the power of inorganic chemistry to provide new knowledge of and new approaches for intervention in biological systems. This will be based on improved understanding of reactions of metal complexes under physiological conditions, on improving the specificity of their interactions, and gaining control over the potential toxicity of synthetic metal complexes. The research programme is highly interdisciplinary involving chemistry, physics, biology and pharmacology, with potential for the discovery of truly novel medicines, especially for the treatment of diseases and conditions which are currently intractable, such as cancer. The challenging and ambitious goals of the present work involve transition metal complexes with novel chemical and biochemical mechanisms of action. They will contain novel features which allow them (i) to be selectively activated by light in cells, or (ii) to be activated by a structural transition, or (ii) exhibit catalytic activity in cells. This ground-breaking research potentially has a very high impact and is based on recent discoveries in the applicant s laboratory. A feature of the programme is the use of state-of-the-art-and-beyond methodology to advance knowledge of medicinal metal coordination chemistry.
Max ERC Funding
1 565 397 €
Duration
Start date: 2010-07-01, End date: 2015-12-31
Project acronym BIOIONS
Project Biological ions in the gas-phase: New techniques for structural characterization of isolated biomolecular ions
Researcher (PI) Caroline Dessent
Host Institution (HI) UNIVERSITY OF YORK
Call Details Starting Grant (StG), PE4, ERC-2007-StG
Summary Recent intensive research on the laser spectroscopy of neutral gas-phase biomolecules has yielded a detailed picture of their structures and conformational preferences away from the complications of the bulk environment. In contrast, work on ionic systems has been sparse despite the fact that many important molecular groups are charged under physiological conditions. To address this probelm, we have developed a custom-built laser spectrometer, which incorporates a distincitive electrospray ionisation (ESI) cluster ion source, dedicated to producing biological anions (ATP,oligonucleotides) and their microsolvated clusters for structural characterization. Many previous laser spectrometers with ESI sources have suffered from producing "hot" congested spectra as the ions were produced at ambient temperatures. This is a particularly serious limitation for spectroscopic studies of biomolecules, since these systems can possess high internal energies due tothe presence of numerous low frequency modes. Our spectrometer overcomes this problem by exploiting the newly developed physics technique of "buffer gas cooling" to produce cold ESI molecular ions. In this proposal, we now seek to exploit the new laser-spectrometer to perform detailed spectroscopic interrogations of ESI generated biomolecular anions and clusters. In addition to traditional ion-dissociation spectroscopies, we propose to develop two new laser spectroscopy techniques (Two-color tuneable IR spectroscopy and Dipole-bound excited state spectroscopy) to give the broadest possible structural characterizations of the systems of interest. Studies will focus on ATP/GTP-anions, olignonucleotides, and sulphated and carboxylated sugars. These methodologies will provide a general approach for performing temperature-controlled spectroscopic characterizations of isolated biological ions, with measurements on the corresponding micro-solvated clusters providing details of how the molecules are perturbed by solvent.
Summary
Recent intensive research on the laser spectroscopy of neutral gas-phase biomolecules has yielded a detailed picture of their structures and conformational preferences away from the complications of the bulk environment. In contrast, work on ionic systems has been sparse despite the fact that many important molecular groups are charged under physiological conditions. To address this probelm, we have developed a custom-built laser spectrometer, which incorporates a distincitive electrospray ionisation (ESI) cluster ion source, dedicated to producing biological anions (ATP,oligonucleotides) and their microsolvated clusters for structural characterization. Many previous laser spectrometers with ESI sources have suffered from producing "hot" congested spectra as the ions were produced at ambient temperatures. This is a particularly serious limitation for spectroscopic studies of biomolecules, since these systems can possess high internal energies due tothe presence of numerous low frequency modes. Our spectrometer overcomes this problem by exploiting the newly developed physics technique of "buffer gas cooling" to produce cold ESI molecular ions. In this proposal, we now seek to exploit the new laser-spectrometer to perform detailed spectroscopic interrogations of ESI generated biomolecular anions and clusters. In addition to traditional ion-dissociation spectroscopies, we propose to develop two new laser spectroscopy techniques (Two-color tuneable IR spectroscopy and Dipole-bound excited state spectroscopy) to give the broadest possible structural characterizations of the systems of interest. Studies will focus on ATP/GTP-anions, olignonucleotides, and sulphated and carboxylated sugars. These methodologies will provide a general approach for performing temperature-controlled spectroscopic characterizations of isolated biological ions, with measurements on the corresponding micro-solvated clusters providing details of how the molecules are perturbed by solvent.
Max ERC Funding
1 250 000 €
Duration
Start date: 2008-10-01, End date: 2015-06-30
Project acronym BIOMOF
Project Biomineral-inspired growth and processing of metal-organic frameworks
Researcher (PI) Darren Bradshaw
Host Institution (HI) UNIVERSITY OF SOUTHAMPTON
Call Details Starting Grant (StG), PE5, ERC-2010-StG_20091028
Summary This ERC-StG proposal, BIOMOF, outlines a dual strategy for the growth and processing of porous metal-organic framework (MOF) materials, inspired by the interfacial interactions that characterise highly controlled biomineralisation processes. The aim is to prepare MOF (bio)-composite materials of hierarchical structure and multi-modal functionality to address key societal challenges in healthcare, catalysis and energy. In order for MOFs to reach their full potential, a transformative approach to their growth, and in particular their processability, is required since the insoluble macroscopic micron-sized crystals resulting from conventional syntheses are unsuitable for many applications. The BIOMOF project defines chemically flexible routes to MOFs under mild conditions, where the added value with respect to wide-ranging experimental procedures for the growth and processing of crystalline controllably nanoscale MOF materials with tunable structure and functionality that display significant porosity for wide-ranging applications is extremely high. Theme 1 exploits protein vesicles and abundant biopolymer matrices for the confined growth of soluble nanoscale MOFs for high-end biomedical applications such as cell imaging and targeted drug delivery, whereas theme 2 focuses on the cost-effective preparation of hierarchically porous MOF composites over several length scales, of relevance to bulk industrial applications such as sustainable catalysis, separations and gas-storage. This diverse yet complementary range of applications arising simply from the way the MOF is processed, coupled with the versatile structural and physical properties of MOFs themselves indicates strongly that the BIOMOF concept is a powerful convergent new approach to applied materials chemistry.
Summary
This ERC-StG proposal, BIOMOF, outlines a dual strategy for the growth and processing of porous metal-organic framework (MOF) materials, inspired by the interfacial interactions that characterise highly controlled biomineralisation processes. The aim is to prepare MOF (bio)-composite materials of hierarchical structure and multi-modal functionality to address key societal challenges in healthcare, catalysis and energy. In order for MOFs to reach their full potential, a transformative approach to their growth, and in particular their processability, is required since the insoluble macroscopic micron-sized crystals resulting from conventional syntheses are unsuitable for many applications. The BIOMOF project defines chemically flexible routes to MOFs under mild conditions, where the added value with respect to wide-ranging experimental procedures for the growth and processing of crystalline controllably nanoscale MOF materials with tunable structure and functionality that display significant porosity for wide-ranging applications is extremely high. Theme 1 exploits protein vesicles and abundant biopolymer matrices for the confined growth of soluble nanoscale MOFs for high-end biomedical applications such as cell imaging and targeted drug delivery, whereas theme 2 focuses on the cost-effective preparation of hierarchically porous MOF composites over several length scales, of relevance to bulk industrial applications such as sustainable catalysis, separations and gas-storage. This diverse yet complementary range of applications arising simply from the way the MOF is processed, coupled with the versatile structural and physical properties of MOFs themselves indicates strongly that the BIOMOF concept is a powerful convergent new approach to applied materials chemistry.
Max ERC Funding
1 492 970 €
Duration
Start date: 2010-11-01, End date: 2015-10-31
Project acronym BioNet
Project Dynamical Redesign of Biomolecular Networks
Researcher (PI) Edina ROSTA
Host Institution (HI) KING'S COLLEGE LONDON
Call Details Starting Grant (StG), PE4, ERC-2017-STG
Summary Enzymes created by Nature are still more selective and can be orders of magnitude more efficient than man-made catalysts, in spite of recent advances in the design of de novo catalysts and in enzyme redesign. The optimal engineering of either small molecular or of complex biological catalysts requires both (i) accurate quantitative computational methods capable of a priori assessing catalytic efficiency, and (ii) molecular design principles and corresponding algorithms to achieve, understand and control biomolecular catalytic function and mechanisms. Presently, the computational design of biocatalysts is challenging due to the need for accurate yet computationally-intensive quantum mechanical calculations of bond formation and cleavage, as well as to the requirement for proper statistical sampling over very many degrees of freedom. Pioneering enhanced sampling and analysis methods have been developed to address crucial challenges bridging the gap between the available simulation length and the biologically relevant timescales. However, biased simulations do not generally permit the direct calculation of kinetic information. Recently, I and others pioneered simulation tools that can enable not only accurate calculations of free energies, but also of the intrinsic molecular kinetics and the underlying reaction mechanisms as well. I propose to develop more robust, automatic, and system-tailored sampling algorithms that are optimal in each case. I will use our kinetics-based methods to develop a novel theoretical framework to address catalytic efficiency and to establish molecular design principles to key design problems for new bio-inspired nanocatalysts, and to identify and characterize small molecule modulators of enzyme activity. This is a highly interdisciplinary project that will enable fundamental advances in molecular simulations and will unveil the physical principles that will lead to design and control of catalysis with Nature-like efficiency.
Summary
Enzymes created by Nature are still more selective and can be orders of magnitude more efficient than man-made catalysts, in spite of recent advances in the design of de novo catalysts and in enzyme redesign. The optimal engineering of either small molecular or of complex biological catalysts requires both (i) accurate quantitative computational methods capable of a priori assessing catalytic efficiency, and (ii) molecular design principles and corresponding algorithms to achieve, understand and control biomolecular catalytic function and mechanisms. Presently, the computational design of biocatalysts is challenging due to the need for accurate yet computationally-intensive quantum mechanical calculations of bond formation and cleavage, as well as to the requirement for proper statistical sampling over very many degrees of freedom. Pioneering enhanced sampling and analysis methods have been developed to address crucial challenges bridging the gap between the available simulation length and the biologically relevant timescales. However, biased simulations do not generally permit the direct calculation of kinetic information. Recently, I and others pioneered simulation tools that can enable not only accurate calculations of free energies, but also of the intrinsic molecular kinetics and the underlying reaction mechanisms as well. I propose to develop more robust, automatic, and system-tailored sampling algorithms that are optimal in each case. I will use our kinetics-based methods to develop a novel theoretical framework to address catalytic efficiency and to establish molecular design principles to key design problems for new bio-inspired nanocatalysts, and to identify and characterize small molecule modulators of enzyme activity. This is a highly interdisciplinary project that will enable fundamental advances in molecular simulations and will unveil the physical principles that will lead to design and control of catalysis with Nature-like efficiency.
Max ERC Funding
1 499 999 €
Duration
Start date: 2018-02-01, End date: 2023-01-31
Project acronym Bionetworking
Project Bionetworking in Asia – A social science approach to international collaboration, informal exchanges, and responsible innovation in the life sciences
Researcher (PI) Margaret Elizabeth Sleeboom-Faulkner
Host Institution (HI) THE UNIVERSITY OF SUSSEX
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary Bio-medical innovation makes a substantial contribution to Western societies and economies. But leading research organisations in the West are increasingly reliant on clinical research conducted beyond the West. Such initiatives are challenged by uncertainties about research quality and therapeutic practices in Asian countries. These only partly justified uncertainties are augmented by unfamiliar conditions. This study examines how to create responsible innovation in the life sciences by looking for ways to overcome existing obstacles to safe, just and ethical international science collaborations.
Building on observations of scientists, managers and patients and supported by Asian language expertise, biology background, and experience with science and technology policy-making, we examine the roles of regional differences and inequalities in the networks used for patient recruitment and international research agreements. Profit-motivated networks in the life sciences also occur underground and at an informal, unregulated level, which we call bionetworking. Bionetworking is a social entrepreneurial activity involving biomedical research, healthcare and patient networks that are maintained by taking advantage of regionally differences in levels of science and technology, healthcare, education and regulatory regimes.
Using novel social-science methods, the project studies two main themes. Theme 1 examines patient recruitment networks for experimental stem cell therapies and cooperation between research and health institutions involving exchanges of patients against other resources. Theme 2 maps and analyses exchanges of biomaterials of human derivation, and forms of ‘ownership’ rights, benefits and burdens associated with their donation, possession, maintenance, and application. Integral analysis of the project nodes incorporates an analysis of public health policy and patient preference in relation to Responsible innovation, Good governance and Global assemblages.
Summary
Bio-medical innovation makes a substantial contribution to Western societies and economies. But leading research organisations in the West are increasingly reliant on clinical research conducted beyond the West. Such initiatives are challenged by uncertainties about research quality and therapeutic practices in Asian countries. These only partly justified uncertainties are augmented by unfamiliar conditions. This study examines how to create responsible innovation in the life sciences by looking for ways to overcome existing obstacles to safe, just and ethical international science collaborations.
Building on observations of scientists, managers and patients and supported by Asian language expertise, biology background, and experience with science and technology policy-making, we examine the roles of regional differences and inequalities in the networks used for patient recruitment and international research agreements. Profit-motivated networks in the life sciences also occur underground and at an informal, unregulated level, which we call bionetworking. Bionetworking is a social entrepreneurial activity involving biomedical research, healthcare and patient networks that are maintained by taking advantage of regionally differences in levels of science and technology, healthcare, education and regulatory regimes.
Using novel social-science methods, the project studies two main themes. Theme 1 examines patient recruitment networks for experimental stem cell therapies and cooperation between research and health institutions involving exchanges of patients against other resources. Theme 2 maps and analyses exchanges of biomaterials of human derivation, and forms of ‘ownership’ rights, benefits and burdens associated with their donation, possession, maintenance, and application. Integral analysis of the project nodes incorporates an analysis of public health policy and patient preference in relation to Responsible innovation, Good governance and Global assemblages.
Max ERC Funding
1 497 711 €
Duration
Start date: 2012-02-01, End date: 2017-01-31
Project acronym BIOPROPERTY
Project Biomedical Research and the Future of Property Rights
Researcher (PI) Javier Lezaun Barreras
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), SH2, ERC-2010-StG_20091209
Summary This research project investigates the dynamics of private and public property in contemporary biomedical research. It will develop an analytical framework combining insights from science and technology studies, economic sociology, and legal and political philosophy, and pursues a social scientific investigation of the evolution of intellectual property rights in three fields of bioscientific research: 1) the use of transgenic research mice; 2) the legal status of totipotent and pluripotent stem cell lines; and 3) modes of collaboration for research and development on neglected diseases. These three domains, and their attendant modes of appropriation, will be compared across three general research themes: a) the production of public scientific goods; b) categories of appropriation; and c) the moral economy of research. The project rests on close observation of research practices in these three domains. The BioProperty research programme will track the trajectories of property rights and property objects in each of the three fields of biomedical research.
Summary
This research project investigates the dynamics of private and public property in contemporary biomedical research. It will develop an analytical framework combining insights from science and technology studies, economic sociology, and legal and political philosophy, and pursues a social scientific investigation of the evolution of intellectual property rights in three fields of bioscientific research: 1) the use of transgenic research mice; 2) the legal status of totipotent and pluripotent stem cell lines; and 3) modes of collaboration for research and development on neglected diseases. These three domains, and their attendant modes of appropriation, will be compared across three general research themes: a) the production of public scientific goods; b) categories of appropriation; and c) the moral economy of research. The project rests on close observation of research practices in these three domains. The BioProperty research programme will track the trajectories of property rights and property objects in each of the three fields of biomedical research.
Max ERC Funding
887 602 €
Duration
Start date: 2011-03-01, End date: 2014-12-31
Project acronym BLINDSPOT
Project Diversity and Performance: Networks of Cognition in Markets and Teams
Researcher (PI) David STARK
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Advanced Grant (AdG), SH2, ERC-2015-AdG
Summary Contemporary organizations face three interrelated, but analytically distinguishable, challenges. First, they should be alert to mistakes that could be catastrophic. Second, they need to allocate attention, especially to correct past mistakes and to make accurate predictions about future developments. Third, they should be innovative, able to stand out from existing categories while being recognized as outstanding. This project investigates these cognitive challenges with the aim of developing a comprehensive sociological approach to study the social properties of cognition. Research on error detection, attention allocation, and recognizant innovation will be conducted in three distinct settings strategically chosen so the scale and complexity of the performance challenges increases across the cases. The research question that cuts across the socio-cognitive challenges asks whether and how diversity contributes to performance. 1) We first test whether social context, understood at the most basic level as the composition of a small collectivity, affects the cognitive activity of pricing. To do so, I use experimental market methods to test whether ethnic and gender diversity deflate price bubbles by disrupting herding behaviour. 2) The second study tests how the social structure of attention affects valuation. The activities involve error correction and accuracy of prediction in estimates by securities analysts; the method is two-mode network analysis; and the timing, intensity, and diversity of attention networks are the effects to be tested. 3) Whereas my first two tests examine relations among competitors, my third examines relations within and across collaborative teams. In studying the network properties of creativity, the challenge is recognizant innovation, the activity involves recording sessions in the field of music, the method is cultural network analysis, and the effects to be tested are the combined effects of stylistic diversity and social structure.
Summary
Contemporary organizations face three interrelated, but analytically distinguishable, challenges. First, they should be alert to mistakes that could be catastrophic. Second, they need to allocate attention, especially to correct past mistakes and to make accurate predictions about future developments. Third, they should be innovative, able to stand out from existing categories while being recognized as outstanding. This project investigates these cognitive challenges with the aim of developing a comprehensive sociological approach to study the social properties of cognition. Research on error detection, attention allocation, and recognizant innovation will be conducted in three distinct settings strategically chosen so the scale and complexity of the performance challenges increases across the cases. The research question that cuts across the socio-cognitive challenges asks whether and how diversity contributes to performance. 1) We first test whether social context, understood at the most basic level as the composition of a small collectivity, affects the cognitive activity of pricing. To do so, I use experimental market methods to test whether ethnic and gender diversity deflate price bubbles by disrupting herding behaviour. 2) The second study tests how the social structure of attention affects valuation. The activities involve error correction and accuracy of prediction in estimates by securities analysts; the method is two-mode network analysis; and the timing, intensity, and diversity of attention networks are the effects to be tested. 3) Whereas my first two tests examine relations among competitors, my third examines relations within and across collaborative teams. In studying the network properties of creativity, the challenge is recognizant innovation, the activity involves recording sessions in the field of music, the method is cultural network analysis, and the effects to be tested are the combined effects of stylistic diversity and social structure.
Max ERC Funding
2 492 033 €
Duration
Start date: 2016-09-01, End date: 2021-08-31
Project acronym CAM-RIG
Project ConfocAl Microscopy and real-time Rheology of dynamIc hyroGels
Researcher (PI) Oren Alexander SCHERMAN
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Consolidator Grant (CoG), PE5, ERC-2016-COG
Summary Hydrogels cross-linked through supramolecular interactions are highly dependant on the dynamic charac- teristics of the physical cross-links. Few fundamental studies have been undertaken to quantitatively de- scribe structure-property relationships for these types of systems. Hydrogels formed from CB[8]-mediated supramolecular physical cross-linking mechanisms have gained significant interest on account of their excel- lent physical and mechanical properties such as self-healing and shear-thinning. This supramolecular motif has been further exploited to introduce and compatibilise a wide variety of different materials into hydrogel networks without phase separation, forming hybrid composite hydrogels attributed with unique and emergent properties. This proposal aims to pioneer the combination of several state-of-the-art characterisation tech- niques into an unique experimental setup (CAM-RIG), which will combine super-resolution and confocal microscopy imaging modalities with simultaneous strain-controlled rheological measurements to investigate fundamental structure-property relationships of these systems. For the first time it will be possible to decon- volute the molecular-level dynamics of the supramolecular physical cross-links from chain entanglement of the polymeric networks and understand their relative contributions on the resultant properties of the hydrogels. Using the fundamental insight gained, a set of key parameters will be determined to maximise the potential of supramolecular biocompatible hydrogels, driving paradigm shifts in sustainable science and biomaterial applications through the precise tuning of physical properties.
Summary
Hydrogels cross-linked through supramolecular interactions are highly dependant on the dynamic charac- teristics of the physical cross-links. Few fundamental studies have been undertaken to quantitatively de- scribe structure-property relationships for these types of systems. Hydrogels formed from CB[8]-mediated supramolecular physical cross-linking mechanisms have gained significant interest on account of their excel- lent physical and mechanical properties such as self-healing and shear-thinning. This supramolecular motif has been further exploited to introduce and compatibilise a wide variety of different materials into hydrogel networks without phase separation, forming hybrid composite hydrogels attributed with unique and emergent properties. This proposal aims to pioneer the combination of several state-of-the-art characterisation tech- niques into an unique experimental setup (CAM-RIG), which will combine super-resolution and confocal microscopy imaging modalities with simultaneous strain-controlled rheological measurements to investigate fundamental structure-property relationships of these systems. For the first time it will be possible to decon- volute the molecular-level dynamics of the supramolecular physical cross-links from chain entanglement of the polymeric networks and understand their relative contributions on the resultant properties of the hydrogels. Using the fundamental insight gained, a set of key parameters will be determined to maximise the potential of supramolecular biocompatible hydrogels, driving paradigm shifts in sustainable science and biomaterial applications through the precise tuning of physical properties.
Max ERC Funding
2 038 120 €
Duration
Start date: 2017-05-01, End date: 2022-04-30
Project acronym CAPRI
Project Chemical and photochemical dynamics of reactions in solution
Researcher (PI) Andrew John Orr-Ewing
Host Institution (HI) UNIVERSITY OF BRISTOL
Call Details Advanced Grant (AdG), PE4, ERC-2011-ADG_20110209
Summary Ultrafast laser methods will be employed to examine the dynamics of chemical and photochemical reactions in liquid solutions. By contrasting the solution phase dynamics with those observed for isolated collisions in the gas phase, the fundamental role of solvent on chemical pathways will be explored at a molecular level. The experimental studies will be complemented by computational simulations that explicitly include treatment of the effects of solvent on reaction energy pathways and reactant and product motions.
The research addresses a major challenge in Chemistry to understand the role of solvent on the mechanisms of chemical reactions. Questions that will be examined include how the solvent modifies reaction barriers and other regions of the reaction potential energy surface (PESs), alters the couplings between PESs, most importantly at conical intersections between electronic states, influences and constrains the dynamical stereochemistry of passage through transition states, and dissipates excess product energy.
The experimental strategy will be to obtain absorption spectra of transient species with lifetimes of ~100 fs – 1000 ps using broad bandwidth light sources in the infrared, visible and ultraviolet regions. Time-evolutions of such spectra reveal the formation and decay of short-lived species that might be highly reactive radicals or internally (vibrationally and electronically) excited molecules. The transient species decay by reaction or energy loss to the solvent. Statistical mechanical theories of reactions in solution treat such processes using linear response theory, but the experimental data will challenge this paradigm by seeking evidence for breakdown of the linear response interaction of solvent and solute on short timescales because of microscopic chemical dynamics that perturb the solvent structure. The work will build on our pioneering experiments at the Rutherford Appleton Laboratory that prove the feasilbility of the methods.
Summary
Ultrafast laser methods will be employed to examine the dynamics of chemical and photochemical reactions in liquid solutions. By contrasting the solution phase dynamics with those observed for isolated collisions in the gas phase, the fundamental role of solvent on chemical pathways will be explored at a molecular level. The experimental studies will be complemented by computational simulations that explicitly include treatment of the effects of solvent on reaction energy pathways and reactant and product motions.
The research addresses a major challenge in Chemistry to understand the role of solvent on the mechanisms of chemical reactions. Questions that will be examined include how the solvent modifies reaction barriers and other regions of the reaction potential energy surface (PESs), alters the couplings between PESs, most importantly at conical intersections between electronic states, influences and constrains the dynamical stereochemistry of passage through transition states, and dissipates excess product energy.
The experimental strategy will be to obtain absorption spectra of transient species with lifetimes of ~100 fs – 1000 ps using broad bandwidth light sources in the infrared, visible and ultraviolet regions. Time-evolutions of such spectra reveal the formation and decay of short-lived species that might be highly reactive radicals or internally (vibrationally and electronically) excited molecules. The transient species decay by reaction or energy loss to the solvent. Statistical mechanical theories of reactions in solution treat such processes using linear response theory, but the experimental data will challenge this paradigm by seeking evidence for breakdown of the linear response interaction of solvent and solute on short timescales because of microscopic chemical dynamics that perturb the solvent structure. The work will build on our pioneering experiments at the Rutherford Appleton Laboratory that prove the feasilbility of the methods.
Max ERC Funding
2 666 684 €
Duration
Start date: 2012-02-01, End date: 2017-01-31
Project acronym CARBONICE
Project Carbon – Ice Composite Materials: Water Structure and Dynamics at the Carbon Interface
Researcher (PI) Christoph Günter SALZMANN
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Consolidator Grant (CoG), PE4, ERC-2016-COG
Summary Carbon and water in its various states of matter make up a substantial proportion of our Universe. The two materials are highly dissimilar with respect to their chemical and physical properties. Elemental carbon is even often referred to as a hydrophobic, ‘water-hating’ material. Yet, the two materials often coexist and critical processes take place at the interface between these unlike chemical species. This includes the hydration shells of hydrophobic moieties in biomolecules, clathrate hydrate materials where water molecules crystallise around hydrophobic guest species as well as icy comets which are often black due to the presence of carbon at their surfaces.
The aim of the CARBONICE project is to investigate the interface and interplay between water and carbon in detail. Using new and innovative experimental strategies, the water molecule will be placed in a variety of different yet highly relevant carbon environments. This will give us unprecedented insights into how water hydrates hydrophobic species which is highly important in the context of hydrophobic interactions. Investigations into how carbon species influence phase transitions of ice will give new insights into crystallisation phenomena but will also reveal the factors that lead to the formation of either ferro- or antiferroelectric ices. Creating carbon – ice composites in the lab as they exist on comets will enable us to understand the complex weather cycles on comets and may help explaining the unusual surface features recently identified by the Rosetta space probe.
In summary, this truly multidisciplinary project opens up a new spyhole to critically important processes at the water – carbon interface. The results will have an impact on the space, atmospheric and general materials sciences but will also be highly relevant with respect to further optimising the computer models of water as well as understanding the properties of water in nano-confinements and how it drives biological processes.
Summary
Carbon and water in its various states of matter make up a substantial proportion of our Universe. The two materials are highly dissimilar with respect to their chemical and physical properties. Elemental carbon is even often referred to as a hydrophobic, ‘water-hating’ material. Yet, the two materials often coexist and critical processes take place at the interface between these unlike chemical species. This includes the hydration shells of hydrophobic moieties in biomolecules, clathrate hydrate materials where water molecules crystallise around hydrophobic guest species as well as icy comets which are often black due to the presence of carbon at their surfaces.
The aim of the CARBONICE project is to investigate the interface and interplay between water and carbon in detail. Using new and innovative experimental strategies, the water molecule will be placed in a variety of different yet highly relevant carbon environments. This will give us unprecedented insights into how water hydrates hydrophobic species which is highly important in the context of hydrophobic interactions. Investigations into how carbon species influence phase transitions of ice will give new insights into crystallisation phenomena but will also reveal the factors that lead to the formation of either ferro- or antiferroelectric ices. Creating carbon – ice composites in the lab as they exist on comets will enable us to understand the complex weather cycles on comets and may help explaining the unusual surface features recently identified by the Rosetta space probe.
In summary, this truly multidisciplinary project opens up a new spyhole to critically important processes at the water – carbon interface. The results will have an impact on the space, atmospheric and general materials sciences but will also be highly relevant with respect to further optimising the computer models of water as well as understanding the properties of water in nano-confinements and how it drives biological processes.
Max ERC Funding
1 999 806 €
Duration
Start date: 2017-06-01, End date: 2022-05-31
Project acronym CARP
Project "Making Selves, Making Revolutions: Comparative Anthropologies of Revolutionary Politics"
Researcher (PI) Martin Holbraad
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Consolidator Grant (CoG), SH2, ERC-2013-CoG
Summary "What kinds of self does it take to make a revolution? And how does revolutionary politics, understood as a project of personal as much as political transformation, articulate with other processes of self-making, such as religious practices? Comparative Anthropologies of Revolutionary Politics (CARP) seeks fundamentally to recast our understanding of revolutions, using their relationship to religious practices in diverse social and cultural settings as a lens through which to reveal revolutions’ varied capacities for self-making. Developing a comparative matrix of revolutionary settings in the Middle East, Latin America and elsewhere, CARP’s core objective is to investigate the differing permutations and dynamics of revolutionary ‘anthropologies’ in the original theological sense of the term, i.e. charting revolutionary politics in relation to varying conceptions of what it is to be human, and of how the horizons of people’s lives are to be understood in relation to divine orders of different kinds, in order to reveal how revolutions come to define what persons may be, deliberately setting the social, political, cultural and ultimately ontological coordinates within which people are made who they are. Bringing close ethnographic investigation to bear on conceptions of revolution, statecraft, and subjectivity in political theory, CARP will produce comprehensive political ethnographies of nine major case-studies, comparing systematically the relationship between revolution and religion in a selection of countries in the Middle East and Latin America. Four smaller-scale case-studies from Europe and Asia will add complementary dimensions to this comparative matrix. Providing much-needed empirical materials and analytical insight into the dynamic comingling of political and religious forms in the making of revolutionary selves, CARP’s ultimate ambition is to launch the comparative study of revolutionary politics as a major new departure for anthropological research."
Summary
"What kinds of self does it take to make a revolution? And how does revolutionary politics, understood as a project of personal as much as political transformation, articulate with other processes of self-making, such as religious practices? Comparative Anthropologies of Revolutionary Politics (CARP) seeks fundamentally to recast our understanding of revolutions, using their relationship to religious practices in diverse social and cultural settings as a lens through which to reveal revolutions’ varied capacities for self-making. Developing a comparative matrix of revolutionary settings in the Middle East, Latin America and elsewhere, CARP’s core objective is to investigate the differing permutations and dynamics of revolutionary ‘anthropologies’ in the original theological sense of the term, i.e. charting revolutionary politics in relation to varying conceptions of what it is to be human, and of how the horizons of people’s lives are to be understood in relation to divine orders of different kinds, in order to reveal how revolutions come to define what persons may be, deliberately setting the social, political, cultural and ultimately ontological coordinates within which people are made who they are. Bringing close ethnographic investigation to bear on conceptions of revolution, statecraft, and subjectivity in political theory, CARP will produce comprehensive political ethnographies of nine major case-studies, comparing systematically the relationship between revolution and religion in a selection of countries in the Middle East and Latin America. Four smaller-scale case-studies from Europe and Asia will add complementary dimensions to this comparative matrix. Providing much-needed empirical materials and analytical insight into the dynamic comingling of political and religious forms in the making of revolutionary selves, CARP’s ultimate ambition is to launch the comparative study of revolutionary politics as a major new departure for anthropological research."
Max ERC Funding
1 854 472 €
Duration
Start date: 2014-06-01, End date: 2019-05-31
Project acronym CASSPIN
Project Comparative Analysis of Social Spaces in Post-Industrial Nations
Researcher (PI) William James Atkinson
Host Institution (HI) UNIVERSITY OF BRISTOL
Call Details Starting Grant (StG), SH2, ERC-2015-STG
Summary The proposed research has two overarching objectives. First, it aims to examine whether it is possible and appropriate to extend a novel way of measuring social class recently devised for the United Kingdom to other post-industrial nations for the purposes of cross-national comparative research. If it is, the project will begin to explore, through secondary and primary analysis of large-scale survey data, the different shapes and trajectories of the class structures – or ‘social spaces’ – of various nation states. This will involve examination of which classes and sub-classes predominate and which have emerged or declined, as well as the different gender and ethnic/nationality constitutions of the classes and the distinct effects these differences have for understanding cultural and political struggles and, ultimately, the distribution of power or ‘recognition’ in each country. Second, the project aims to explore, through both statistical analysis and qualitative interviews, how social class is actually lived, experienced and balanced against other pressures and sources of recognition in everyday life, with a focus on three specific nations: the United States, Germany and Sweden. Of particular interest in this respect is the balancing of desire for recognition through money and education – the two cornerstones of social class in post-industrial capitalist societies – and their associated lifestyles with desires for recognition and love within the family. The comparative analysis included in both research aims will be guided by the hypothesis that national differences depend on the nature of the welfare regime in operation, especially as it relates to the nature and extent of workforce feminisation, though the research will also be alive to the possibility of alternative – or no significant – sources of contrast.
Summary
The proposed research has two overarching objectives. First, it aims to examine whether it is possible and appropriate to extend a novel way of measuring social class recently devised for the United Kingdom to other post-industrial nations for the purposes of cross-national comparative research. If it is, the project will begin to explore, through secondary and primary analysis of large-scale survey data, the different shapes and trajectories of the class structures – or ‘social spaces’ – of various nation states. This will involve examination of which classes and sub-classes predominate and which have emerged or declined, as well as the different gender and ethnic/nationality constitutions of the classes and the distinct effects these differences have for understanding cultural and political struggles and, ultimately, the distribution of power or ‘recognition’ in each country. Second, the project aims to explore, through both statistical analysis and qualitative interviews, how social class is actually lived, experienced and balanced against other pressures and sources of recognition in everyday life, with a focus on three specific nations: the United States, Germany and Sweden. Of particular interest in this respect is the balancing of desire for recognition through money and education – the two cornerstones of social class in post-industrial capitalist societies – and their associated lifestyles with desires for recognition and love within the family. The comparative analysis included in both research aims will be guided by the hypothesis that national differences depend on the nature of the welfare regime in operation, especially as it relates to the nature and extent of workforce feminisation, though the research will also be alive to the possibility of alternative – or no significant – sources of contrast.
Max ERC Funding
1 467 038 €
Duration
Start date: 2016-05-01, End date: 2021-04-30
Project acronym CatHet
Project New Catalytic Asymmetric Strategies for N-Heterocycle Synthesis
Researcher (PI) John Forwood Bower
Host Institution (HI) UNIVERSITY OF BRISTOL
Call Details Starting Grant (StG), PE5, ERC-2014-STG
Summary Medicinal chemistry requires more efficient and diverse methods for the asymmetric synthesis of chiral scaffolds. Over 60% of the world’s top selling small molecule drug compounds are chiral and, of these, approximately 80% are marketed as single enantiomers. There is a compelling correlation between drug candidate “chiral complexity” and the likelihood of progression to the marketplace. Surprisingly, and despite the tremendous advances made in catalysis over the past several decades, the “chiral complexity” of drug discovery libraries has actually decreased, while, at the same time, for the reasons mentioned above, the “chiral complexity” of marketed drugs has increased. Since the mid-1990s, there has been a notable acceleration of this “complexity divergence”. Consequently, there is now an urgent need to provide efficient processes that directly access privileged chiral scaffolds. It is our philosophy that catalysis holds the key here and new processes should be based upon platforms that can exert control over both absolute and relative stereochemistry. In this proposal we outline the development of a range of N-heteroannulation processes based upon the catalytic generation and trapping of unique or unusual classes of organometallic intermediate derived from transition metal insertion into C-C and C-N sigma-bonds. We will provide a variety of enabling methodologies and demonstrate applicability in flexible total syntheses of important natural product scaffolds. The processes proposed are synthetically flexible, operationally simple and amenable to asymmetric catalysis. Likely starting points, based upon preliminary results, will set the stage for the realisation of aspirational and transformative goals. Through the study of the organometallic intermediates involved here, there is potential to generalise these new catalytic manifolds, such that this research will transcend N heterocyclic chemistry to provide enabling methods for organic chemistry as a whole.
Summary
Medicinal chemistry requires more efficient and diverse methods for the asymmetric synthesis of chiral scaffolds. Over 60% of the world’s top selling small molecule drug compounds are chiral and, of these, approximately 80% are marketed as single enantiomers. There is a compelling correlation between drug candidate “chiral complexity” and the likelihood of progression to the marketplace. Surprisingly, and despite the tremendous advances made in catalysis over the past several decades, the “chiral complexity” of drug discovery libraries has actually decreased, while, at the same time, for the reasons mentioned above, the “chiral complexity” of marketed drugs has increased. Since the mid-1990s, there has been a notable acceleration of this “complexity divergence”. Consequently, there is now an urgent need to provide efficient processes that directly access privileged chiral scaffolds. It is our philosophy that catalysis holds the key here and new processes should be based upon platforms that can exert control over both absolute and relative stereochemistry. In this proposal we outline the development of a range of N-heteroannulation processes based upon the catalytic generation and trapping of unique or unusual classes of organometallic intermediate derived from transition metal insertion into C-C and C-N sigma-bonds. We will provide a variety of enabling methodologies and demonstrate applicability in flexible total syntheses of important natural product scaffolds. The processes proposed are synthetically flexible, operationally simple and amenable to asymmetric catalysis. Likely starting points, based upon preliminary results, will set the stage for the realisation of aspirational and transformative goals. Through the study of the organometallic intermediates involved here, there is potential to generalise these new catalytic manifolds, such that this research will transcend N heterocyclic chemistry to provide enabling methods for organic chemistry as a whole.
Max ERC Funding
1 548 738 €
Duration
Start date: 2015-04-01, End date: 2020-03-31
Project acronym CAtMolChip
Project Cold Atmospheric Molecules on a Chip
Researcher (PI) Stephen Dermot Hogan
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Consolidator Grant (CoG), PE4, ERC-2015-CoG
Summary Highly excited electronic states of small atmospheric molecules play an important, but as yet little explored, role in the reactivity, and in the evolution of plasmas, including the Aurora Borealis, in the upper atmosphere of the Earth. Processes involving these highly excited states are very challenging to investigate theoretically because of the high density of states close to the ionization limits where they lie. Therefore, experimental input is essential for the identification of the reaction and decay mechanisms, and the quantum states of importance in future studies. However, experimental techniques that can be exploited to provide this input have only become available very recently. These techniques permit gas-phase molecular samples in these highly excited states to be confined in traps for sufficient lengths of time (e.g. 1 ms – 10 ms) for detailed studies to be performed in a controlled laboratory environment. They include resonance-enhanced and non-resonance-enhanced multiphoton excitation of long-lived high angular momentum Rydberg states of small molecules, and chip-based devices for efficiently decelerating, transporting and trapping these samples.
With the support of this Consolidator Grant a new experimental research program will be developed in the Department of Physics and Astronomy at University College London involving laboratory based studies of (1) inelastic scattering processes, and (2) the decay mechanisms of gas-phase atmospheric molecules, including N2, O2 and NO, and their constituent atoms, in high Rydberg states. The planned experiments will be directed toward understanding the effects of static and time-dependent electric and magnetic fields, and blackbody radiation fields on slow dissociation processes that occur in highly excited states of N2, O2 and NO, investigations of collisional energy transfer processes, and studies of the role that these excited electronic states play in the evolution and reactivity of atmospheric plasmas incl
Summary
Highly excited electronic states of small atmospheric molecules play an important, but as yet little explored, role in the reactivity, and in the evolution of plasmas, including the Aurora Borealis, in the upper atmosphere of the Earth. Processes involving these highly excited states are very challenging to investigate theoretically because of the high density of states close to the ionization limits where they lie. Therefore, experimental input is essential for the identification of the reaction and decay mechanisms, and the quantum states of importance in future studies. However, experimental techniques that can be exploited to provide this input have only become available very recently. These techniques permit gas-phase molecular samples in these highly excited states to be confined in traps for sufficient lengths of time (e.g. 1 ms – 10 ms) for detailed studies to be performed in a controlled laboratory environment. They include resonance-enhanced and non-resonance-enhanced multiphoton excitation of long-lived high angular momentum Rydberg states of small molecules, and chip-based devices for efficiently decelerating, transporting and trapping these samples.
With the support of this Consolidator Grant a new experimental research program will be developed in the Department of Physics and Astronomy at University College London involving laboratory based studies of (1) inelastic scattering processes, and (2) the decay mechanisms of gas-phase atmospheric molecules, including N2, O2 and NO, and their constituent atoms, in high Rydberg states. The planned experiments will be directed toward understanding the effects of static and time-dependent electric and magnetic fields, and blackbody radiation fields on slow dissociation processes that occur in highly excited states of N2, O2 and NO, investigations of collisional energy transfer processes, and studies of the role that these excited electronic states play in the evolution and reactivity of atmospheric plasmas incl
Max ERC Funding
1 985 553 €
Duration
Start date: 2016-06-01, End date: 2021-05-31
Project acronym CCLAD
Project The Politics of Climate Change Loss and Damage
Researcher (PI) Lisa VANHALA
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), SH2, ERC-2017-STG
Summary The way in which normative principles (“norms”) matter in world politics is now a key area of international relations research. Yet we have limited understanding of why some norms emerge and gain traction globally whereas others do not. The politics of loss and damage related to climate change offers a paradigm case for studying the emergence of - and contestation over - norms, specifically justice norms. The parties to the UN Framework Convention on Climate Change (UNFCCC) have recently acknowledged that there is an urgent need to address the inevitable, irreversible consequences of climate change. Yet within this highly contested policy area - which includes work on disaster risk reduction; non-economic losses (e.g. loss of sovereignty); finance and climate-related migration - there is little consensus about what loss and damage policy means or what it requires of the global community, of states and of the (current and future) victims of climate change. Relying on an interdisciplinary theoretical approach and an ethnographic methodology that traverses scales of governance, my project - The Politics of Climate Change Loss and Damage (CCLAD) - will elucidate the conditions under which a norm is likely to become hegemonic, influential, contested or reversed by introducing a new understanding of the fluid nature of norm-content. I argue that norms are partly constituted through the practices of policy-making and implementation at the international and national level. The research will examine the micro-politics of the international negotiations and implementation of loss and damage policy and also involves cross-national comparative research on domestic loss and damage policy practices. Bringing these two streams of work together will allow me to show how and why policy practices shape the evolution of climate justice norms. CCLAD will also make an important methodological contribution through the development of political ethnography and “practice-tracing” methods.
Summary
The way in which normative principles (“norms”) matter in world politics is now a key area of international relations research. Yet we have limited understanding of why some norms emerge and gain traction globally whereas others do not. The politics of loss and damage related to climate change offers a paradigm case for studying the emergence of - and contestation over - norms, specifically justice norms. The parties to the UN Framework Convention on Climate Change (UNFCCC) have recently acknowledged that there is an urgent need to address the inevitable, irreversible consequences of climate change. Yet within this highly contested policy area - which includes work on disaster risk reduction; non-economic losses (e.g. loss of sovereignty); finance and climate-related migration - there is little consensus about what loss and damage policy means or what it requires of the global community, of states and of the (current and future) victims of climate change. Relying on an interdisciplinary theoretical approach and an ethnographic methodology that traverses scales of governance, my project - The Politics of Climate Change Loss and Damage (CCLAD) - will elucidate the conditions under which a norm is likely to become hegemonic, influential, contested or reversed by introducing a new understanding of the fluid nature of norm-content. I argue that norms are partly constituted through the practices of policy-making and implementation at the international and national level. The research will examine the micro-politics of the international negotiations and implementation of loss and damage policy and also involves cross-national comparative research on domestic loss and damage policy practices. Bringing these two streams of work together will allow me to show how and why policy practices shape the evolution of climate justice norms. CCLAD will also make an important methodological contribution through the development of political ethnography and “practice-tracing” methods.
Max ERC Funding
1 471 530 €
Duration
Start date: 2018-05-01, End date: 2023-04-30
Project acronym CHEMBIOMECH
Project Exploring mechanism in chemical biology by high-throughput approaches
Researcher (PI) Florian Hollfelder
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Starting Grant (StG), PE4, ERC-2007-StG
Summary In the biomedical sciences, where endless combinatorial diversity of genes, proteins and synthetic molecules is involved, miniaturisation has not simply allowed an increase in the speed at which experiment can be performed: it has given birth to new areas such as combinatorial chemistry and biology, proteomics, genomics, and more recently, systems and synthetic biology. In all these areas, the synthesis, assay and analysis of large molecular ensembles has become the essence of experimental progress. However, it is the systematic analysis of the enormous amounts of data generated that will ultimately lead to an understanding of fundamental chemical and biological problems. This proposal deals with approaches in which libraries of molecules are employed to give such mechanistic insight – into how enzyme catalysis is brought about in proteins and polymeric enzyme models and into the molecular recognition and cell biology of drug delivery reagents. In each case considerable technical challenges are involved in the way diversity is brought about and probed: ranging from either using the tools of synthetic chemistry to using gene repertoires in emulsion microdroplet reactors with femtolitre volumes, handled in microfluidic devices.
Summary
In the biomedical sciences, where endless combinatorial diversity of genes, proteins and synthetic molecules is involved, miniaturisation has not simply allowed an increase in the speed at which experiment can be performed: it has given birth to new areas such as combinatorial chemistry and biology, proteomics, genomics, and more recently, systems and synthetic biology. In all these areas, the synthesis, assay and analysis of large molecular ensembles has become the essence of experimental progress. However, it is the systematic analysis of the enormous amounts of data generated that will ultimately lead to an understanding of fundamental chemical and biological problems. This proposal deals with approaches in which libraries of molecules are employed to give such mechanistic insight – into how enzyme catalysis is brought about in proteins and polymeric enzyme models and into the molecular recognition and cell biology of drug delivery reagents. In each case considerable technical challenges are involved in the way diversity is brought about and probed: ranging from either using the tools of synthetic chemistry to using gene repertoires in emulsion microdroplet reactors with femtolitre volumes, handled in microfluidic devices.
Max ERC Funding
563 848 €
Duration
Start date: 2008-09-01, End date: 2013-08-31
Project acronym ChemNav
Project Magnetic sensing by molecules, birds, and devices
Researcher (PI) Peter John Hore
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Advanced Grant (AdG), PE4, ERC-2013-ADG
Summary The sensory mechanisms that allow birds to perceive the direction of the Earth’s magnetic field for the purpose of navigation are only now beginning to be understood. One of the two leading hypotheses is founded on magnetically sensitive photochemical reactions in the retina. It is thought that transient photo-induced radical pairs in cryptochrome, a blue-light photoreceptor protein, act as the primary magnetic sensor. Experimental and theoretical support for this mechanism has been accumulating over the last few years, qualifying chemical magnetoreception for a place in the emerging field of Quantum Biology.
In this proposal, we aim to determine the detailed principles of efficient chemical sensing of weak magnetic fields, to elucidate the biophysics of animal compass magnetoreception, and to explore the possibilities of magnetic sensing technologies inspired by the coherent dynamics of entangled electron spins in cryptochrome-based radical pairs.
We will:
(a) Establish the fundamental structural, kinetic, dynamic and magnetic properties that allow efficient chemical sensing of Earth-strength magnetic fields in cryptochromes.
(b) Devise new, sensitive forms of optical spectroscopy for this purpose.
(c) Design, construct and iteratively refine non-natural proteins (maquettes) as versatile model systems for testing and optimising molecular magnetoreceptors.
(d) Characterise the spin dynamics and magnetic sensitivity of maquette magnetoreceptors using specialised magnetic resonance and optical spectroscopic techniques.
(e) Develop efficient and accurate methods for simulating the coherent spin dynamics of realistic radical pairs in order to interpret experimental data, guide the implementation of new experiments, test concepts of magnetoreceptor function, and guide the design of efficient sensors.
(f) Explore the feasibility of electronically addressable, organic semiconductor sensors inspired by radical pair magnetoreception.
Summary
The sensory mechanisms that allow birds to perceive the direction of the Earth’s magnetic field for the purpose of navigation are only now beginning to be understood. One of the two leading hypotheses is founded on magnetically sensitive photochemical reactions in the retina. It is thought that transient photo-induced radical pairs in cryptochrome, a blue-light photoreceptor protein, act as the primary magnetic sensor. Experimental and theoretical support for this mechanism has been accumulating over the last few years, qualifying chemical magnetoreception for a place in the emerging field of Quantum Biology.
In this proposal, we aim to determine the detailed principles of efficient chemical sensing of weak magnetic fields, to elucidate the biophysics of animal compass magnetoreception, and to explore the possibilities of magnetic sensing technologies inspired by the coherent dynamics of entangled electron spins in cryptochrome-based radical pairs.
We will:
(a) Establish the fundamental structural, kinetic, dynamic and magnetic properties that allow efficient chemical sensing of Earth-strength magnetic fields in cryptochromes.
(b) Devise new, sensitive forms of optical spectroscopy for this purpose.
(c) Design, construct and iteratively refine non-natural proteins (maquettes) as versatile model systems for testing and optimising molecular magnetoreceptors.
(d) Characterise the spin dynamics and magnetic sensitivity of maquette magnetoreceptors using specialised magnetic resonance and optical spectroscopic techniques.
(e) Develop efficient and accurate methods for simulating the coherent spin dynamics of realistic radical pairs in order to interpret experimental data, guide the implementation of new experiments, test concepts of magnetoreceptor function, and guide the design of efficient sensors.
(f) Explore the feasibility of electronically addressable, organic semiconductor sensors inspired by radical pair magnetoreception.
Max ERC Funding
2 997 062 €
Duration
Start date: 2013-12-01, End date: 2018-11-30
Project acronym CheSSTaG
Project Chemotactic Super-Selective Targeting of Gliomas
Researcher (PI) Giuseppe BATTAGLIA
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Consolidator Grant (CoG), PE5, ERC-2017-COG
Summary I propose here a research program aimed to the design a completely new platform for drug delivery. I will combine our existing repertoire of molecular engineering tools based around our established approach to design responsive nanoparticles known as Polymersomes to integrate new features using clinically safe and biodegradable components that will make them super-selective and chemotactic toward glucose gradients so to deliver large therapeutic payload into the central nervous systems and the brain in particular targeting cancer cells harbouring within the healthy. We will do so by engineering components using supramolecular interaction inspired by biological complexity equipping carriers with the ability to self-propelled as a function of glucose gradient. I will complement our proposed design with advanced biological characterisation associating functional information arising form the physiological barrier to structural parameters integrated into the final carrier design.
Summary
I propose here a research program aimed to the design a completely new platform for drug delivery. I will combine our existing repertoire of molecular engineering tools based around our established approach to design responsive nanoparticles known as Polymersomes to integrate new features using clinically safe and biodegradable components that will make them super-selective and chemotactic toward glucose gradients so to deliver large therapeutic payload into the central nervous systems and the brain in particular targeting cancer cells harbouring within the healthy. We will do so by engineering components using supramolecular interaction inspired by biological complexity equipping carriers with the ability to self-propelled as a function of glucose gradient. I will complement our proposed design with advanced biological characterisation associating functional information arising form the physiological barrier to structural parameters integrated into the final carrier design.
Max ERC Funding
2 081 747 €
Duration
Start date: 2018-05-01, End date: 2023-04-30
Project acronym CITIZENSENSE
Project Citizen Sensing and Environmental Practice: Assessing Participatory Engagements with Environments through Sensor Technologies
Researcher (PI) Jennifer Gabrys
Host Institution (HI) GOLDSMITHS' COLLEGE
Call Details Starting Grant (StG), SH2, ERC-2012-StG_20111124
Summary This project will investigate, through three case studies, the relationship between technologies and practices of environmental sensing and citizen engagement. Wireless sensors, which are an increasing part of digital communication infrastructures, are commonly deployed for environmental monitoring within scientific study. Practices of monitoring and sensing environments have migrated to a number of everyday participatory applications, where users of smart phones and networked devices are able to engage with similar modes of environmental observation and data collection. Such “citizen sensing” projects intend to democratize the collection and use of environmental sensor data in order to facilitate expanded citizen engagement in environmental issues. But how effective are these practices of citizen sensing in not just providing “crowd-sourced” data sets, but also in giving rise to new modes of environmental awareness and practice? Through intensive fieldwork, study and use of sensing applications, the case studies will set out to contextualize, question and expand upon the understandings and possibilities of democratized environmental action through citizen sensing practices. The first case study, “Wild Sensing,” will focus on the use of sensors to map and track flora and fauna activity and habitats. The second case study, “Pollution Sensing,” will concentrate on the increasing use of sensors to detect environmental disturbance, including air and water pollution. The third case study will investigate “Urban Sensing,” and will focus on urban sustainability or “smart city” projects that implement sensor technologies to realize more efficient or environmentally sound urban processes.
Summary
This project will investigate, through three case studies, the relationship between technologies and practices of environmental sensing and citizen engagement. Wireless sensors, which are an increasing part of digital communication infrastructures, are commonly deployed for environmental monitoring within scientific study. Practices of monitoring and sensing environments have migrated to a number of everyday participatory applications, where users of smart phones and networked devices are able to engage with similar modes of environmental observation and data collection. Such “citizen sensing” projects intend to democratize the collection and use of environmental sensor data in order to facilitate expanded citizen engagement in environmental issues. But how effective are these practices of citizen sensing in not just providing “crowd-sourced” data sets, but also in giving rise to new modes of environmental awareness and practice? Through intensive fieldwork, study and use of sensing applications, the case studies will set out to contextualize, question and expand upon the understandings and possibilities of democratized environmental action through citizen sensing practices. The first case study, “Wild Sensing,” will focus on the use of sensors to map and track flora and fauna activity and habitats. The second case study, “Pollution Sensing,” will concentrate on the increasing use of sensors to detect environmental disturbance, including air and water pollution. The third case study will investigate “Urban Sensing,” and will focus on urban sustainability or “smart city” projects that implement sensor technologies to realize more efficient or environmentally sound urban processes.
Max ERC Funding
1 500 000 €
Duration
Start date: 2013-01-01, End date: 2017-12-31
Project acronym CITSEE
Project The Europeanisation of Citizenship in the Successor States of the Former Yugoslavia
Researcher (PI) Josephine Shaw
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Advanced Grant (AdG), SH2, ERC-2008-AdG
Summary CITSEE is a comparative and contextualised study of the citizenship regimes of the seven successor states of the former Yugoslavia (SFRY) in their broader European context. It focuses on the relationship between how these regimes have developed after the disintegration of SFRY and the processes of re-integration occurring in the context of the enlargement of the European Union applied in the region. It makes use of the varied statuses under EU law of the SFRY successor states, of which only Slovenia is so far a Member State. The processes at the heart of the study include the effects of previous and prospective enlargements of the EU and the broader stabilisation and association processes. CITSEE uses methods which look at legal and institutional change in its broader political context and applies the broad approach of constitutional ethnography. It has national case studies and thematic case studies of key issues which have a transnational dimension, including the status of residents of the former SFRY Republics resident in other Republics at the moment of independence, dual and multiple nationality, the granting or denial of political rights for resident non-nationals and non-resident nationals, the status of minorities such as the Roma, gender issues arising in a citizenship context, and the impact of citizenship concepts on free movement and travel across borders. While CITSEE s objectives are not normative in nature, and are not intended to supply answers as to best or worst practices in relation to citizenship regimes, or to evaluate the impact of Europeanisation as negative or positive, none the less such an evaluative study is likely to be of interest not only to researchers, but also to NGOs and to policy-makers in the region and in the EU and other international institutions because it fills in many gaps in our current knowledge and provides improved evidence on the basis of which policies may be developed in the future.
Summary
CITSEE is a comparative and contextualised study of the citizenship regimes of the seven successor states of the former Yugoslavia (SFRY) in their broader European context. It focuses on the relationship between how these regimes have developed after the disintegration of SFRY and the processes of re-integration occurring in the context of the enlargement of the European Union applied in the region. It makes use of the varied statuses under EU law of the SFRY successor states, of which only Slovenia is so far a Member State. The processes at the heart of the study include the effects of previous and prospective enlargements of the EU and the broader stabilisation and association processes. CITSEE uses methods which look at legal and institutional change in its broader political context and applies the broad approach of constitutional ethnography. It has national case studies and thematic case studies of key issues which have a transnational dimension, including the status of residents of the former SFRY Republics resident in other Republics at the moment of independence, dual and multiple nationality, the granting or denial of political rights for resident non-nationals and non-resident nationals, the status of minorities such as the Roma, gender issues arising in a citizenship context, and the impact of citizenship concepts on free movement and travel across borders. While CITSEE s objectives are not normative in nature, and are not intended to supply answers as to best or worst practices in relation to citizenship regimes, or to evaluate the impact of Europeanisation as negative or positive, none the less such an evaluative study is likely to be of interest not only to researchers, but also to NGOs and to policy-makers in the region and in the EU and other international institutions because it fills in many gaps in our current knowledge and provides improved evidence on the basis of which policies may be developed in the future.
Max ERC Funding
2 240 000 €
Duration
Start date: 2009-04-01, End date: 2014-12-31
Project acronym CLD
Project China, Law, and Development
Researcher (PI) Matthew ERIE
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), SH2, ERC-2018-STG
Summary The world is in the midst of a sea change in approaches to development. The rise of nationalist politics in the U.S., U.K. and Europe have questioned commitments to global governance at the same time that China has emerged as a champion of globalization, a turn of geo-political events that would have been unfathomable ten years ago. Through its own multi-lateral institutions, China is setting a new agenda for development from Europe to Oceania. China’s approach differs from Anglo/Euro/American approaches to “law and development” (LD). Whereas LD orthodoxy has sought to improve legal institutions in poor states, Chinese do not foster rule of law abroad. Instead, Chinese view law as one set of rules, among others, to facilitate economic transactions and not to foster democratization. This distinction has sparked a global debate about the so-called “China model” as an alternative to LD. Yet there is little empirical data with which to assess the means and ends of China’s expanded footprint, a question with long-term implications for much of the developing world. This project addresses that problem by proposing that even if Chinese cross-border development does not operate through transparent rules, it nonetheless has its own notion of order. The project adopts a multi-sited, mixed method, and interdisciplinary approach—at the intersection of comparative law, developmental studies, and legal anthropology—to understand the nature of China’s order. The project has two objectives:
1. To establish the conceptual bases for the study of China’s approach to law and development by developing the first systematic study of the impacts of Chinese investment on the legal systems of developing economies.
2. To experiment with a comparative research design to theorize how China’s approach suggests a type of order that extends through a conjuncture of regional and local processes and manifests itself differently in diverse contexts.
Summary
The world is in the midst of a sea change in approaches to development. The rise of nationalist politics in the U.S., U.K. and Europe have questioned commitments to global governance at the same time that China has emerged as a champion of globalization, a turn of geo-political events that would have been unfathomable ten years ago. Through its own multi-lateral institutions, China is setting a new agenda for development from Europe to Oceania. China’s approach differs from Anglo/Euro/American approaches to “law and development” (LD). Whereas LD orthodoxy has sought to improve legal institutions in poor states, Chinese do not foster rule of law abroad. Instead, Chinese view law as one set of rules, among others, to facilitate economic transactions and not to foster democratization. This distinction has sparked a global debate about the so-called “China model” as an alternative to LD. Yet there is little empirical data with which to assess the means and ends of China’s expanded footprint, a question with long-term implications for much of the developing world. This project addresses that problem by proposing that even if Chinese cross-border development does not operate through transparent rules, it nonetheless has its own notion of order. The project adopts a multi-sited, mixed method, and interdisciplinary approach—at the intersection of comparative law, developmental studies, and legal anthropology—to understand the nature of China’s order. The project has two objectives:
1. To establish the conceptual bases for the study of China’s approach to law and development by developing the first systematic study of the impacts of Chinese investment on the legal systems of developing economies.
2. To experiment with a comparative research design to theorize how China’s approach suggests a type of order that extends through a conjuncture of regional and local processes and manifests itself differently in diverse contexts.
Max ERC Funding
1 499 381 €
Duration
Start date: 2019-01-01, End date: 2023-12-31
Project acronym CNTBBB
Project Targeting potential of carbon nanotubes at the blood brain barrier
Researcher (PI) Alexandra Elizabeth Porter
Host Institution (HI) IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Call Details Starting Grant (StG), PE5, ERC-2010-StG_20091028
Summary Targeted drug delivery across the blood brain barrier (BBB) to the central nervous system is a large challenge for the treatment of neurological disorders. This 4 year ERC program is aimed towards the evaluating the BBB penetration capacity and toxicological potential of novel carbon nanotube (CNT) carriers using an integrated multidisciplinary approach. State-of-art characterisation techniques developed by the PI will be applied and further developed to detect the interaction of carbon nanotubes with in vitro BBB model and neuronal cells. Specific aims:
1. Identify the mechanisms of translocation of CNT across the endothelial cells which comprise the BBB, as well as uptake by neuronal cells in vitro.
2. To investigate the effect of length, diameter and surface charge of CNTs on the BBB and neuronal cells penetration capacity in vitro.
3. To investigate the toxicological profile of CNT on the BBB and the various neuronal cell types (immortalised and primary neuronal cultures).
4. Develop protocols to assess whether the CNTs degrade inside the cell.
The ERC Grant will consolidate the new Research Group in nanomaterials-cell interfaces, and allow them to perform stimulating investigator-initiated frontier research in nanotoxicology and nanomedicine. To this end, a multi-disciplinary laboratory will be realized within the framework of this 4-year the ERC Programme. This will permit the group around the PI, to expand activities, push limits, create new boundaries, and develop new protocols for studying nanoparticle-cell interactions in close collaboration with ICL s Department of medicine and chemistry. Within the proposed program there is an underlying ambition both to gain a fundamental understanding for which parameters of CNTs determine their penetration capacity through the BBB and also to assess their toxicological potential at the BBB two highlighted themes by the ERC.
Summary
Targeted drug delivery across the blood brain barrier (BBB) to the central nervous system is a large challenge for the treatment of neurological disorders. This 4 year ERC program is aimed towards the evaluating the BBB penetration capacity and toxicological potential of novel carbon nanotube (CNT) carriers using an integrated multidisciplinary approach. State-of-art characterisation techniques developed by the PI will be applied and further developed to detect the interaction of carbon nanotubes with in vitro BBB model and neuronal cells. Specific aims:
1. Identify the mechanisms of translocation of CNT across the endothelial cells which comprise the BBB, as well as uptake by neuronal cells in vitro.
2. To investigate the effect of length, diameter and surface charge of CNTs on the BBB and neuronal cells penetration capacity in vitro.
3. To investigate the toxicological profile of CNT on the BBB and the various neuronal cell types (immortalised and primary neuronal cultures).
4. Develop protocols to assess whether the CNTs degrade inside the cell.
The ERC Grant will consolidate the new Research Group in nanomaterials-cell interfaces, and allow them to perform stimulating investigator-initiated frontier research in nanotoxicology and nanomedicine. To this end, a multi-disciplinary laboratory will be realized within the framework of this 4-year the ERC Programme. This will permit the group around the PI, to expand activities, push limits, create new boundaries, and develop new protocols for studying nanoparticle-cell interactions in close collaboration with ICL s Department of medicine and chemistry. Within the proposed program there is an underlying ambition both to gain a fundamental understanding for which parameters of CNTs determine their penetration capacity through the BBB and also to assess their toxicological potential at the BBB two highlighted themes by the ERC.
Max ERC Funding
1 229 998 €
Duration
Start date: 2011-02-01, End date: 2017-01-31
Project acronym COLORLANDS
Project COLOR Ordering Templated by Hierarchized Supramolecular Porous FlatLANDS
Researcher (PI) Davide Bonifazi
Host Institution (HI) CARDIFF UNIVERSITY
Call Details Starting Grant (StG), PE5, ERC-2011-StG_20101014
Summary The idea of this research project is to take advantage of molecular self-assembly to create a new generation of periodically-organized porous organic materials that, acting as specific molecular hosts, can structurally control the positioning of multiple functional guests on surfaces, opening new horizons toward the understanding and development of rationale protocols for the patterning of unprecedented materials. Taking advantage of a supramolecular approach to engineer extended mono- and two-dimensional organic networks, the ultimate aim of COLORLANDS is to create novel hosting frameworks accommodating in a predetermined fashion organic chromophores and/or fluorophores. For instance, these can be oligophenylenes as blue emitters, cumarines/oligophenylethylenes as green emitters, or perylenebisimides conjugates as red emitters. Depending on their spatial organization, such materials will be the springboard for further technological development in the fields of electroluminescent devices or artificial leafs mimicking natural light harvesting antenna systems. The self-assembly of selected rigid molecular modules alternatively functionalized with complementary connectors (PNA strands) will yield, under equilibrium conditions, one exclusive structural pattern. This will feature controllable (in shape, size and chemical nature) periodic receptor sites, each programmed to selectively accommodate a specific molecular chromophore and/or fluorophore. Particular attention will be given to the design and fundamental understanding of specific orthogonal interactions between the self-assembled receptor sites and the functional molecular guests. This will be achieved through the lateral organic functionalization of the PNA strands with novel orthogonal H-bonding-based recognition motifs. Depending on the ratio between the different receptors, one can tailor the desired emission or absorption colour, virtually enabling unlimited surfing through the color coordinate diagram.
Summary
The idea of this research project is to take advantage of molecular self-assembly to create a new generation of periodically-organized porous organic materials that, acting as specific molecular hosts, can structurally control the positioning of multiple functional guests on surfaces, opening new horizons toward the understanding and development of rationale protocols for the patterning of unprecedented materials. Taking advantage of a supramolecular approach to engineer extended mono- and two-dimensional organic networks, the ultimate aim of COLORLANDS is to create novel hosting frameworks accommodating in a predetermined fashion organic chromophores and/or fluorophores. For instance, these can be oligophenylenes as blue emitters, cumarines/oligophenylethylenes as green emitters, or perylenebisimides conjugates as red emitters. Depending on their spatial organization, such materials will be the springboard for further technological development in the fields of electroluminescent devices or artificial leafs mimicking natural light harvesting antenna systems. The self-assembly of selected rigid molecular modules alternatively functionalized with complementary connectors (PNA strands) will yield, under equilibrium conditions, one exclusive structural pattern. This will feature controllable (in shape, size and chemical nature) periodic receptor sites, each programmed to selectively accommodate a specific molecular chromophore and/or fluorophore. Particular attention will be given to the design and fundamental understanding of specific orthogonal interactions between the self-assembled receptor sites and the functional molecular guests. This will be achieved through the lateral organic functionalization of the PNA strands with novel orthogonal H-bonding-based recognition motifs. Depending on the ratio between the different receptors, one can tailor the desired emission or absorption colour, virtually enabling unlimited surfing through the color coordinate diagram.
Max ERC Funding
1 295 400 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym COMBATTRAUMA
Project From warfare to welfare: a comparative study of how combat trauma is internalized and institutionalized
Researcher (PI) Alexander Bangs Edmonds
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Starting Grant (StG), SH2, ERC-2012-StG_20111124
Summary This project is an anthropological study of combat trauma in three Western nations: Israel, the United States, and the Netherlands. Trauma means different things to different actors, and acquires a different value (both economic and social) in different therapeutic settings. Research will examine how clinical notions of combat trauma are established, adapted, resisted or internalized in different nations. It will result in a comparative framework for understanding how combat trauma is shaped by two major modern institutions: the military and psychiatry. Methodologically, it combines ethnographic fieldwork with veterans, research on clinical practices, and analysis of the policies and discourses that institutionalize combat trauma. Unusual within trauma studies, it aims to shed light on potentially conflicting values about violence and suffering in military and psychiatric instiutions, which may be less apparent to researchers trained within those institutions. By analyzing how veterans and clinicians perceive ethnicity, it will also contribute to understanding of the experiences of subordinate ethnic groups in military and psychiatric institutions. It is expected to identify key problems in the delivery of good care to veterans and have an impact on policy and healthcare. Theoretically, it will advance studies of biopolitics and medicalization. Existing theories tend to minimize how patients contest clinical models of illness. The moral significance of violence in combat trauma may, however, create particular kinds of resistance to clinical illness models – an issue that has not been previously addressed. This study will make a major contribution to understanding how war related suffering is internalized and institutionalized as clinical illness. It will also advance social science studies of psychiatry during a time when the field is undergoing a major and controversial move towards a biological approach to mental illness.
Summary
This project is an anthropological study of combat trauma in three Western nations: Israel, the United States, and the Netherlands. Trauma means different things to different actors, and acquires a different value (both economic and social) in different therapeutic settings. Research will examine how clinical notions of combat trauma are established, adapted, resisted or internalized in different nations. It will result in a comparative framework for understanding how combat trauma is shaped by two major modern institutions: the military and psychiatry. Methodologically, it combines ethnographic fieldwork with veterans, research on clinical practices, and analysis of the policies and discourses that institutionalize combat trauma. Unusual within trauma studies, it aims to shed light on potentially conflicting values about violence and suffering in military and psychiatric instiutions, which may be less apparent to researchers trained within those institutions. By analyzing how veterans and clinicians perceive ethnicity, it will also contribute to understanding of the experiences of subordinate ethnic groups in military and psychiatric institutions. It is expected to identify key problems in the delivery of good care to veterans and have an impact on policy and healthcare. Theoretically, it will advance studies of biopolitics and medicalization. Existing theories tend to minimize how patients contest clinical models of illness. The moral significance of violence in combat trauma may, however, create particular kinds of resistance to clinical illness models – an issue that has not been previously addressed. This study will make a major contribution to understanding how war related suffering is internalized and institutionalized as clinical illness. It will also advance social science studies of psychiatry during a time when the field is undergoing a major and controversial move towards a biological approach to mental illness.
Max ERC Funding
1 492 086 €
Duration
Start date: 2013-08-01, End date: 2018-07-31
Project acronym CoMMaD
Project Computational Molecular Materials Discovery
Researcher (PI) Kim JELFS
Host Institution (HI) IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Call Details Starting Grant (StG), PE5, ERC-2017-STG
Summary The objective of the project is to develop a computational approach to accelerate the discovery of molecular materials. These materials will include porous molecules, small organic molecules and macromolecular polymers, which have application as a result of either their porosity or optoelectronic properties. The applications that will be targeted include in molecular separations, sensing, (photo)catalysis and photovoltaics. To achieve my aims, I will screen libraries of building blocks through a combination of techniques including evolutionary algorithms and machine learning. Through the application of cheminformatics algorithms, I will target the most promising libraries, assess synthetic diversity and accessibility and analyse structure-property relationships. I will develop software that will predict the (macro)molecular structures and properties; the molecular property screening calculations will include void characterisation, binding energies, diffusion barriers, local assembly, charge transport and energy level assessment. A consideration of synthetic accessibility at every stage will be central to my approach, which will ensure the realisation of our predicted targets. I have several synthetic collaborators who can provide pathways to synthetic realisation. Improved materials in this field have the potential to either reduce our energy needs or provide renewable energy, helping the EU meet the targets of the 2030 Energy Strategy.
Summary
The objective of the project is to develop a computational approach to accelerate the discovery of molecular materials. These materials will include porous molecules, small organic molecules and macromolecular polymers, which have application as a result of either their porosity or optoelectronic properties. The applications that will be targeted include in molecular separations, sensing, (photo)catalysis and photovoltaics. To achieve my aims, I will screen libraries of building blocks through a combination of techniques including evolutionary algorithms and machine learning. Through the application of cheminformatics algorithms, I will target the most promising libraries, assess synthetic diversity and accessibility and analyse structure-property relationships. I will develop software that will predict the (macro)molecular structures and properties; the molecular property screening calculations will include void characterisation, binding energies, diffusion barriers, local assembly, charge transport and energy level assessment. A consideration of synthetic accessibility at every stage will be central to my approach, which will ensure the realisation of our predicted targets. I have several synthetic collaborators who can provide pathways to synthetic realisation. Improved materials in this field have the potential to either reduce our energy needs or provide renewable energy, helping the EU meet the targets of the 2030 Energy Strategy.
Max ERC Funding
1 499 390 €
Duration
Start date: 2018-04-01, End date: 2023-03-31
Project acronym COMPEN
Project Penal Policymaking and the prisoner experience: a comparative analysis
Researcher (PI) Benjamin Crewe
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Consolidator Grant (CoG), SH2, ERC-2014-CoG
Summary Recent years have seen renewed interest in the political economy of punishment, yet almost no attention has been given to the factors that translate socio-political arrangements into penal practices or the specific nature of imprisonment in different political-economic systems. Based on research in England & Wales and one Nordic nation, the project goals are to expose the dynamics of the penal state and the nature of penality in countries that are considered ‘exclusionary’ and ‘inclusionary’ respectively in their socio-economic and penal practices. These goals will be achieved through four comparative sub-projects: first, a study of penal policymaking and the ‘penal field’ (the players and processes that shape penal policy and practice); second, an exploration of the texture of imprisonment for women and sex offenders, groups presumed to experience inclusionary and exclusionary penal practices in distinctive ways; third, a study of how these prisoners experience entry into and exit from the system; fourth, a study of the ‘deep end’ imprisonment in both countries.
A central aim is to interrogate widespread assumptions about the relative mildness/severity of penal practices in inclusionary and exclusionary nations. The research will employ an emerging framework that conceptualises the prison experience through notions of ‘depth’, ‘weight’, ‘tightness’ and ‘breadth’. It will foreground the roles of shame and guilt in shaping prisoners’ orientations, concepts that feature in theories of offending and reintegration, but are absent from the sociology of imprisonment. Through the concept of ‘penal consciousness’, the project will also explore the interaction between the punitive intentions of the state and prisoners’ perceptions of the purposes and legitimacy of their punishment. The research will be groundbreaking in several ways, reshaping the field of comparative penology, and linking macro issues of the penal state with the lived realities of the prison landings.
Summary
Recent years have seen renewed interest in the political economy of punishment, yet almost no attention has been given to the factors that translate socio-political arrangements into penal practices or the specific nature of imprisonment in different political-economic systems. Based on research in England & Wales and one Nordic nation, the project goals are to expose the dynamics of the penal state and the nature of penality in countries that are considered ‘exclusionary’ and ‘inclusionary’ respectively in their socio-economic and penal practices. These goals will be achieved through four comparative sub-projects: first, a study of penal policymaking and the ‘penal field’ (the players and processes that shape penal policy and practice); second, an exploration of the texture of imprisonment for women and sex offenders, groups presumed to experience inclusionary and exclusionary penal practices in distinctive ways; third, a study of how these prisoners experience entry into and exit from the system; fourth, a study of the ‘deep end’ imprisonment in both countries.
A central aim is to interrogate widespread assumptions about the relative mildness/severity of penal practices in inclusionary and exclusionary nations. The research will employ an emerging framework that conceptualises the prison experience through notions of ‘depth’, ‘weight’, ‘tightness’ and ‘breadth’. It will foreground the roles of shame and guilt in shaping prisoners’ orientations, concepts that feature in theories of offending and reintegration, but are absent from the sociology of imprisonment. Through the concept of ‘penal consciousness’, the project will also explore the interaction between the punitive intentions of the state and prisoners’ perceptions of the purposes and legitimacy of their punishment. The research will be groundbreaking in several ways, reshaping the field of comparative penology, and linking macro issues of the penal state with the lived realities of the prison landings.
Max ERC Funding
1 964 948 €
Duration
Start date: 2015-09-01, End date: 2020-08-31
Project acronym complexNMR
Project Structural Dynamics of Protein Complexes by Solid-State NMR
Researcher (PI) Józef Romuald Lewandowski
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Starting Grant (StG), PE4, ERC-2014-STG
Summary Multidrug resistant bacteria that render worthless the current arsenal of antibiotics are a growing global problem. This grave challenge could be tackled by polyketide synthases (PKSs), which are gigantic modular enzymatic assembly lines for natural products. PKSs could be developed for industry to produce chemically difficult to synthesize drugs, but cannot be harnessed until we understand how they work on the molecular level. However, such understanding is missing because we cannot easily investigate large complexes with current structural biology and modeling methods. A key puzzle is how the function of these multicomponent systems emerges from atomic-scale interactions of their parts. Solving this puzzle requires a holistic approach involving measuring and modeling the relevant interacting parts together.
Our goal is to develop a multidisciplinary approach rooted in solid and solution state NMR that will make possible studies of complexes from PKSs. The two main challenges for the NMR of PKSs are increasing sensitivity and resolution. Recent innovations from our lab allow application of solid-state to study large complexes in 2–10 nanomole quantities. Building on this approach, with a protein-antibody complex as a test case, we will develop new NMR methods that will enable a study of structure and motions of domains in complexes. We will probe, for the first time, the structural dynamics of PKSs of enacyloxin and gladiolin, which are antibiotics against life-threatening multidrug resistant hospital-acquired Acinetobacter baumannii infections and tuberculosis. These studies will guide rational engineering of the PKSs to enable synthetic biology approaches to produce new antibiotics.
If successful, this project will go beyond the state of the art by: enabling studies of unknown proteins in large complexes and providing unique insights into novel mechanisms for controlling biosynthesis in PKSs, turning them into truly programmable synthetic biology devices.
Summary
Multidrug resistant bacteria that render worthless the current arsenal of antibiotics are a growing global problem. This grave challenge could be tackled by polyketide synthases (PKSs), which are gigantic modular enzymatic assembly lines for natural products. PKSs could be developed for industry to produce chemically difficult to synthesize drugs, but cannot be harnessed until we understand how they work on the molecular level. However, such understanding is missing because we cannot easily investigate large complexes with current structural biology and modeling methods. A key puzzle is how the function of these multicomponent systems emerges from atomic-scale interactions of their parts. Solving this puzzle requires a holistic approach involving measuring and modeling the relevant interacting parts together.
Our goal is to develop a multidisciplinary approach rooted in solid and solution state NMR that will make possible studies of complexes from PKSs. The two main challenges for the NMR of PKSs are increasing sensitivity and resolution. Recent innovations from our lab allow application of solid-state to study large complexes in 2–10 nanomole quantities. Building on this approach, with a protein-antibody complex as a test case, we will develop new NMR methods that will enable a study of structure and motions of domains in complexes. We will probe, for the first time, the structural dynamics of PKSs of enacyloxin and gladiolin, which are antibiotics against life-threatening multidrug resistant hospital-acquired Acinetobacter baumannii infections and tuberculosis. These studies will guide rational engineering of the PKSs to enable synthetic biology approaches to produce new antibiotics.
If successful, this project will go beyond the state of the art by: enabling studies of unknown proteins in large complexes and providing unique insights into novel mechanisms for controlling biosynthesis in PKSs, turning them into truly programmable synthetic biology devices.
Max ERC Funding
1 999 044 €
Duration
Start date: 2015-05-01, End date: 2020-04-30
Project acronym COMPLEXORDER
Project The Complexity Revolution: Exploiting Unconventional Order in Next-Generation Materials Design
Researcher (PI) Andrew GOODWIN
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Advanced Grant (AdG), PE5, ERC-2017-ADG
Summary The fundamental objective of the research described in this proposal is to lay the foundations for understanding how structural complexity can give rise to materials properties inaccessible to structurally-simple states. The long-term vision is a paradigm shift in the way we as chemists design materials—the “Complexity Revolution”—where we move to thinking beyond the unit cell and harness unconventional order to generate emergent states with entirely novel behaviour. The key methodologies of the project are (i) exploitation of the rich structural information accessible using 3D-PDF / diffuse scattering techniques, (ii) exploration of the phase behaviour of unconventional ordered states using computational methods, and (iii) experimental/computational studies of a broad range of materials in which complexity arises from a large variety of different phenemona. In this way, the project will establish how we might controllably introduce complexity into materials by varying chemical composition and synthesis, how we might then characterise these complex states, and how we might exploit this complexity when designing next-generation materials with unprecedented electronic, catalytic, photonic, information storage, dielectric, topological, and magnetic properties.
Summary
The fundamental objective of the research described in this proposal is to lay the foundations for understanding how structural complexity can give rise to materials properties inaccessible to structurally-simple states. The long-term vision is a paradigm shift in the way we as chemists design materials—the “Complexity Revolution”—where we move to thinking beyond the unit cell and harness unconventional order to generate emergent states with entirely novel behaviour. The key methodologies of the project are (i) exploitation of the rich structural information accessible using 3D-PDF / diffuse scattering techniques, (ii) exploration of the phase behaviour of unconventional ordered states using computational methods, and (iii) experimental/computational studies of a broad range of materials in which complexity arises from a large variety of different phenemona. In this way, the project will establish how we might controllably introduce complexity into materials by varying chemical composition and synthesis, how we might then characterise these complex states, and how we might exploit this complexity when designing next-generation materials with unprecedented electronic, catalytic, photonic, information storage, dielectric, topological, and magnetic properties.
Max ERC Funding
3 362 635 €
Duration
Start date: 2018-10-01, End date: 2023-09-30
Project acronym COMPROP
Project Computational Propaganda:Investigating the Impact of Algorithms and Bots on Political Discourse in Europe
Researcher (PI) Philip Howard
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Consolidator Grant (CoG), SH2, ERC-2014-CoG
Summary Social media can have an impressive impact on civic engagement and political discourse. Yet increasingly we find political actors using digital media and automated scripts for social control. Computational propaganda—through bots, botnets, and algorithms—has become one of the most concerning impacts of technology innovation. Unfortunately, bot identification and impact analysis are among the most difficult research challenges facing the social and computer sciences.
COMPROP objectives are to advance a) rigorous social and computer science on bot use, b) critical theory on digital manipulation and political outcomes, c) our understanding of how social media propaganda impacts social movement organization and vitality. This project will innovate through i) “real-time” social and information science actively disseminated to journalists, researchers, policy experts and the interested public, ii) the first detailed data set of political bot activity, iii) deepened expertise through cultivation of a regional expert network able to detect bots and their impact in Europe.
COMPROP will achieve this through multi-method and reflexive work packages: 1) international qualitative fieldwork with teams of bot makers and computer scientists working to detect bots; 2a) construction of an original event data set of incidents of political bot use and 2b) treatment of the data set with fuzzy set and traditional statistics; 3) computational theory for detecting political bots and 4) a sustained dissemination strategy. This project will employ state-of-the-art “network ethnography” techniques, use the latest fuzzy set / qualitative comparative statistics, and advance computational theory on bot detection via cutting-edge algorithmic work enhanced by new crowd-sourcing techniques.
Political bots are already being deployed over social networks in Europe. COMPROP will put the best methods in social and computer science to work on the size of the problem and the possible solutions.
Summary
Social media can have an impressive impact on civic engagement and political discourse. Yet increasingly we find political actors using digital media and automated scripts for social control. Computational propaganda—through bots, botnets, and algorithms—has become one of the most concerning impacts of technology innovation. Unfortunately, bot identification and impact analysis are among the most difficult research challenges facing the social and computer sciences.
COMPROP objectives are to advance a) rigorous social and computer science on bot use, b) critical theory on digital manipulation and political outcomes, c) our understanding of how social media propaganda impacts social movement organization and vitality. This project will innovate through i) “real-time” social and information science actively disseminated to journalists, researchers, policy experts and the interested public, ii) the first detailed data set of political bot activity, iii) deepened expertise through cultivation of a regional expert network able to detect bots and their impact in Europe.
COMPROP will achieve this through multi-method and reflexive work packages: 1) international qualitative fieldwork with teams of bot makers and computer scientists working to detect bots; 2a) construction of an original event data set of incidents of political bot use and 2b) treatment of the data set with fuzzy set and traditional statistics; 3) computational theory for detecting political bots and 4) a sustained dissemination strategy. This project will employ state-of-the-art “network ethnography” techniques, use the latest fuzzy set / qualitative comparative statistics, and advance computational theory on bot detection via cutting-edge algorithmic work enhanced by new crowd-sourcing techniques.
Political bots are already being deployed over social networks in Europe. COMPROP will put the best methods in social and computer science to work on the size of the problem and the possible solutions.
Max ERC Funding
1 980 112 €
Duration
Start date: 2016-01-01, End date: 2020-12-31
Project acronym COMPSELF
Project Self-Organisation: From Molecules to Matter
Researcher (PI) David John Wales
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Advanced Grant (AdG), PE4, ERC-2010-AdG_20100224
Summary This research proposal concerns the theory and computer simulation of self-organisation to predict properties and to design systems with specified characteristics. The key computational challenge is to explore the energy landscape for complex systems and make predictions to characterise efficient self-organisation on experimental time and length scales. Novel methodology is required to overcome the problems of broken ergodicity and rare events. The theoretical framework exploits stationary points of the potential energy landscape to access the required time and length scales. Applications include self-assembly of mesoscopic structures from coarse-grained building blocks and all-atom simulations of conformational changes in specific proteins and nucleic acids.
We aim to establish design principles for efficient self-assembly by developing novel tools for visualising and exploration of the corresponding landscape. Here, a key issue is how the interactions between the constituent particles determine the organisation of the energy landscape. Identifying which features lead to successful self-assembly and which disrupt such ordering will lead to a wide range of important applications, ranging from design of new materials to identifying new anti-viral drugs. The same methodology will be applied to detailed models of specific biomolecules, where self-organisation into alternative structures is associated with disease. Global optimisation will be employed in structure prediction for variable pathogens, such as human influenza virus. Pathways for folding and misfolding of specific proteins and nucleic acids will be characterised using novel rare events methodology, providing insight into intermediates that could serve as potential drug targets.
Summary
This research proposal concerns the theory and computer simulation of self-organisation to predict properties and to design systems with specified characteristics. The key computational challenge is to explore the energy landscape for complex systems and make predictions to characterise efficient self-organisation on experimental time and length scales. Novel methodology is required to overcome the problems of broken ergodicity and rare events. The theoretical framework exploits stationary points of the potential energy landscape to access the required time and length scales. Applications include self-assembly of mesoscopic structures from coarse-grained building blocks and all-atom simulations of conformational changes in specific proteins and nucleic acids.
We aim to establish design principles for efficient self-assembly by developing novel tools for visualising and exploration of the corresponding landscape. Here, a key issue is how the interactions between the constituent particles determine the organisation of the energy landscape. Identifying which features lead to successful self-assembly and which disrupt such ordering will lead to a wide range of important applications, ranging from design of new materials to identifying new anti-viral drugs. The same methodology will be applied to detailed models of specific biomolecules, where self-organisation into alternative structures is associated with disease. Global optimisation will be employed in structure prediction for variable pathogens, such as human influenza virus. Pathways for folding and misfolding of specific proteins and nucleic acids will be characterised using novel rare events methodology, providing insight into intermediates that could serve as potential drug targets.
Max ERC Funding
2 069 374 €
Duration
Start date: 2011-03-01, End date: 2016-02-29
Project acronym ConflictNET
Project The Politics and Practice of Social Media in Conflict
Researcher (PI) Nicole STREMLAU
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), SH2, ERC-2016-STG
Summary Over the next five years an unprecedented number of initiatives will coalesce, contributing to an extension of the reach of the Internet to the world’s most remote regions. While previous efforts to expand Internet access have focused on urban areas, current initiatives are leveraging new technologies from drones to satellites to provide affordable access to the worlds poorest, many of whom are in Africa and live in regions where the state is weak and there is protracted violent conflict. Current debates have largely focused on technical issues of improving access, or assumed ways that technology will help ‘liberate’ populations or improve governance. This project focuses on a key puzzle that is often overlooked: How does increased access to social media affect the balance between peace-building efforts and attempts perpetuate violence in conflict-affected communities?
With a focus on Africa (and particularly on religious and political violence in Eastern Africa), this project will investigate the relationship between social media and conflict through three research questions at the macro, meso and micro level: how are social media altering the transnational dimensions of conflict and peacebuilding? How are public authorities reacting to, and appropriating, social media to either encourage violence or promote peace? And in what ways are social media changing the way people experience, participate in, or respond to violent conflict? It will examine these questions in the context of dangerous speech online; the exit and entry of individuals away from, and into, conflict; the tactics and strategies actors adopt to shape the Internet; and how governance actors are leveraging social media in conflict-affected communities.
Summary
Over the next five years an unprecedented number of initiatives will coalesce, contributing to an extension of the reach of the Internet to the world’s most remote regions. While previous efforts to expand Internet access have focused on urban areas, current initiatives are leveraging new technologies from drones to satellites to provide affordable access to the worlds poorest, many of whom are in Africa and live in regions where the state is weak and there is protracted violent conflict. Current debates have largely focused on technical issues of improving access, or assumed ways that technology will help ‘liberate’ populations or improve governance. This project focuses on a key puzzle that is often overlooked: How does increased access to social media affect the balance between peace-building efforts and attempts perpetuate violence in conflict-affected communities?
With a focus on Africa (and particularly on religious and political violence in Eastern Africa), this project will investigate the relationship between social media and conflict through three research questions at the macro, meso and micro level: how are social media altering the transnational dimensions of conflict and peacebuilding? How are public authorities reacting to, and appropriating, social media to either encourage violence or promote peace? And in what ways are social media changing the way people experience, participate in, or respond to violent conflict? It will examine these questions in the context of dangerous speech online; the exit and entry of individuals away from, and into, conflict; the tactics and strategies actors adopt to shape the Internet; and how governance actors are leveraging social media in conflict-affected communities.
Max ERC Funding
1 499 450 €
Duration
Start date: 2017-08-01, End date: 2022-07-31
Project acronym CONNECTORS
Project Connectors – an international study into the development of children’s everyday practices of participation in circuits of social action
Researcher (PI) Sevasti Melissa Nolas
Host Institution (HI) GOLDSMITHS' COLLEGE
Call Details Starting Grant (StG), SH2, ERC-2013-StG
Summary Participation – defined in this project as the social practice of engaging in personal and social change – links private and public life, biography and history, and forms a mechanism for social action. Twenty years after the ratification of the United Nations Convention for the Rights of the Child (1989) the international community is no closer to identifying what constitutes a ‘good enough’ model for understanding and supporting the development of children’s participation in public life. The project asks game changing questions about the emergence of children’s orientation towards social action through qualitative, longitudinal and cross-national research. Building on biographical interviews with children, relational and geographical mapping techniques, selective participant-observation with children, and children social research workshops in three cities (London, Athens, Mumbai), the project examines the meaning of personal and social change in middle childhood (6-11 year olds), the circuits of social action that children tap into in an attempt to make changes real, the extent to which privilege, marginalization and economic crisis shape children’s practices of participation, and the ways in which encounters with difference (gender, ethnicity, race, religion) challenge children’s orientation towards social action. By sampling children from a diverse cross-section of each city the project will collect and follow a total of 100 children over a five-year period. The project will provide a rich data sources for making within and between country comparisons and in doing so enable the development a theoretical paradigm for understanding children’s participation that is derived from the bottom-up, that is generated in diverse settings, including non-Western, and that takes advantage of the current rupture to established socio-economic realities to ask questions about the future of social action.
Summary
Participation – defined in this project as the social practice of engaging in personal and social change – links private and public life, biography and history, and forms a mechanism for social action. Twenty years after the ratification of the United Nations Convention for the Rights of the Child (1989) the international community is no closer to identifying what constitutes a ‘good enough’ model for understanding and supporting the development of children’s participation in public life. The project asks game changing questions about the emergence of children’s orientation towards social action through qualitative, longitudinal and cross-national research. Building on biographical interviews with children, relational and geographical mapping techniques, selective participant-observation with children, and children social research workshops in three cities (London, Athens, Mumbai), the project examines the meaning of personal and social change in middle childhood (6-11 year olds), the circuits of social action that children tap into in an attempt to make changes real, the extent to which privilege, marginalization and economic crisis shape children’s practices of participation, and the ways in which encounters with difference (gender, ethnicity, race, religion) challenge children’s orientation towards social action. By sampling children from a diverse cross-section of each city the project will collect and follow a total of 100 children over a five-year period. The project will provide a rich data sources for making within and between country comparisons and in doing so enable the development a theoretical paradigm for understanding children’s participation that is derived from the bottom-up, that is generated in diverse settings, including non-Western, and that takes advantage of the current rupture to established socio-economic realities to ask questions about the future of social action.
Max ERC Funding
1 469 296 €
Duration
Start date: 2014-03-01, End date: 2019-02-28
Project acronym CONSTEURGLOBGOV
Project The Role and Future of National Constitutions in European and Global Governance
Researcher (PI) Anneli Albi
Host Institution (HI) UNIVERSITY OF KENT
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary At a time when the discourse on constitutionalism has come to focus on the constitutionalisation processes at the European and global level, this project will turn the spotlight on national constitutions. It embarks on an analysis and rethinking of the role and future of national constitutions in the context where decision-making has increasingly shifted to transnational level. The project will have three objectives. The first objective is concerned with the role of constitutions internally within the state: the project assesses how credible the content of constitutions remains given the realities of European integration. To this end, it will undertake a comprehensive, comparative and issue-based analysis of EU-related amendments in national constitutions. The second objective concerns the role of constitutions externally with regard to European integration. While national constitutions have increasingly been regarded as a manifestation of sovereignty, and therefore representing values that are often viewed as parochial, the project will turn the focus on other values contained in the constitutions, such as protection of rights and the rule of law. It will explore constitutional courts’ judgements articulating the rights and values that mandate upholding at supranational level, and assess the responsiveness of the European Court of Justice with regard to such concerns. The third objective applies experiences from the EU context to the new research area of global governance. The project aims to assess whether the constitutional provisions on international treaties suffice to reflect the sheer extent to which decision-making has shifted to international institutions and global regulatory networks. It will also explore how constitutions could respond to the problems increasingly highlighted in the context of global governance in relation to legitimacy, democratic control, accountability and the rule of law.
Summary
At a time when the discourse on constitutionalism has come to focus on the constitutionalisation processes at the European and global level, this project will turn the spotlight on national constitutions. It embarks on an analysis and rethinking of the role and future of national constitutions in the context where decision-making has increasingly shifted to transnational level. The project will have three objectives. The first objective is concerned with the role of constitutions internally within the state: the project assesses how credible the content of constitutions remains given the realities of European integration. To this end, it will undertake a comprehensive, comparative and issue-based analysis of EU-related amendments in national constitutions. The second objective concerns the role of constitutions externally with regard to European integration. While national constitutions have increasingly been regarded as a manifestation of sovereignty, and therefore representing values that are often viewed as parochial, the project will turn the focus on other values contained in the constitutions, such as protection of rights and the rule of law. It will explore constitutional courts’ judgements articulating the rights and values that mandate upholding at supranational level, and assess the responsiveness of the European Court of Justice with regard to such concerns. The third objective applies experiences from the EU context to the new research area of global governance. The project aims to assess whether the constitutional provisions on international treaties suffice to reflect the sheer extent to which decision-making has shifted to international institutions and global regulatory networks. It will also explore how constitutions could respond to the problems increasingly highlighted in the context of global governance in relation to legitimacy, democratic control, accountability and the rule of law.
Max ERC Funding
1 230 958 €
Duration
Start date: 2012-01-01, End date: 2018-12-31
Project acronym CONTREX
Project Controlling Triplet Excitons in Organic Semiconductors
Researcher (PI) Hugo Bronstein
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Starting Grant (StG), PE5, ERC-2015-STG
Summary The urgent need to reduce carbon emissions in order to mitigate climate change requires the development of clean, renewable energy sources. Solar power offers a virtually unlimited supply of energy, providing it can be harnessed efficiently. Traditional silicon solar cells demonstrate high performance (~20%) but their required method of manufacture prohibits large area production rendering them too expensive to be used on a global scale. Organic solar cells (made from conjugated polymers and fullerenes) have the potential to be fabricated by low cost printing methods allowing for large scale modules to be produced cheaply. Conventional organic solar cells function by generating charge from a singlet excited state. In order to achieve optimum performance the precise morphology of polymer and fullerene must be controlled which can be extremely challenging. These devices however, have attained good efficiencies (10%) but are hampered by severe loss mechanisms which generally involve the formation of a lower energy triplet excited state.
We propose to develop novel materials for organic solar cells which will instead utilise this triplet excited state to generate charges. This will enable us to not only eliminate this loss mechanism but due to the unique properties of the triplet excited state will allow for numerous benefits. Firstly, the long lifetime of the triplet excited state will be exploited to allow for a simpler organic solar cell where precise morphological control is not required. Secondly, the proposed new materials will allow for the utilisation of near-IR light which is typically wasted in ALL current solar cell devices. Thirdly, exploiting a unique photophysical process we will produce materials capable of delivering efficiencies in excess of the theoretical limit available to conventional solar cells. Thus we propose that utilisation of triplet excitons is the required step-change to allow for organic solar cells to achieve their ultimate efficiencies
Summary
The urgent need to reduce carbon emissions in order to mitigate climate change requires the development of clean, renewable energy sources. Solar power offers a virtually unlimited supply of energy, providing it can be harnessed efficiently. Traditional silicon solar cells demonstrate high performance (~20%) but their required method of manufacture prohibits large area production rendering them too expensive to be used on a global scale. Organic solar cells (made from conjugated polymers and fullerenes) have the potential to be fabricated by low cost printing methods allowing for large scale modules to be produced cheaply. Conventional organic solar cells function by generating charge from a singlet excited state. In order to achieve optimum performance the precise morphology of polymer and fullerene must be controlled which can be extremely challenging. These devices however, have attained good efficiencies (10%) but are hampered by severe loss mechanisms which generally involve the formation of a lower energy triplet excited state.
We propose to develop novel materials for organic solar cells which will instead utilise this triplet excited state to generate charges. This will enable us to not only eliminate this loss mechanism but due to the unique properties of the triplet excited state will allow for numerous benefits. Firstly, the long lifetime of the triplet excited state will be exploited to allow for a simpler organic solar cell where precise morphological control is not required. Secondly, the proposed new materials will allow for the utilisation of near-IR light which is typically wasted in ALL current solar cell devices. Thirdly, exploiting a unique photophysical process we will produce materials capable of delivering efficiencies in excess of the theoretical limit available to conventional solar cells. Thus we propose that utilisation of triplet excitons is the required step-change to allow for organic solar cells to achieve their ultimate efficiencies
Max ERC Funding
1 499 223 €
Duration
Start date: 2016-04-01, End date: 2021-03-31
Project acronym CONTROL
Project Laser control over crystal nucleation
Researcher (PI) Klaas Wijnne
Host Institution (HI) UNIVERSITY OF GLASGOW
Call Details Advanced Grant (AdG), PE4, ERC-2018-ADG
Summary The CONTROL programme I propose here is a five-year programme of frontier research to develop a novel platform for the manipulation of phase transitions, crystal nucleation, and polymorph control based on a novel optical-tweezing technique and plasmonics. About 20 years ago, it was shown that lasers can nucleate crystals in super-saturated solution and might even be able to select the polymorph that crystallises. However, no theoretical model was found explaining the results and little progress was made.
In a recent publication (Nat. Chem. 10, 506 (2018)), we showed that laser-induced nucleation can be understood in terms of the harnessing of concentration fluctuations near a liquid–liquid critical point using optical tweezing. This breakthrough opens the way to a research programme with risky, ambitious, and ground-breaking long-term aims: full control over crystal nucleation including chirality and polymorphism.
New optical and microscopic techniques will be developed to allow laser manipulation on a massively parallel scale and chiral nucleation using twisted light. Systematically characterising and manipulating the phase behaviour of mixtures, will allow the use of the optical-tweezing effect to effectively control the crystallisation of small molecules, peptides, proteins, and polymers. Exploiting nanostructures will allow parallelisation on a vast scale and fine control over chirality and polymorph selection through plasmonic tweezing. Even partial success in the five years of the programme will lead to fundamental new insights and technological breakthroughs. These breakthroughs will be exploited for future commercial applications towards the end of the project.
Summary
The CONTROL programme I propose here is a five-year programme of frontier research to develop a novel platform for the manipulation of phase transitions, crystal nucleation, and polymorph control based on a novel optical-tweezing technique and plasmonics. About 20 years ago, it was shown that lasers can nucleate crystals in super-saturated solution and might even be able to select the polymorph that crystallises. However, no theoretical model was found explaining the results and little progress was made.
In a recent publication (Nat. Chem. 10, 506 (2018)), we showed that laser-induced nucleation can be understood in terms of the harnessing of concentration fluctuations near a liquid–liquid critical point using optical tweezing. This breakthrough opens the way to a research programme with risky, ambitious, and ground-breaking long-term aims: full control over crystal nucleation including chirality and polymorphism.
New optical and microscopic techniques will be developed to allow laser manipulation on a massively parallel scale and chiral nucleation using twisted light. Systematically characterising and manipulating the phase behaviour of mixtures, will allow the use of the optical-tweezing effect to effectively control the crystallisation of small molecules, peptides, proteins, and polymers. Exploiting nanostructures will allow parallelisation on a vast scale and fine control over chirality and polymorph selection through plasmonic tweezing. Even partial success in the five years of the programme will lead to fundamental new insights and technological breakthroughs. These breakthroughs will be exploited for future commercial applications towards the end of the project.
Max ERC Funding
2 488 162 €
Duration
Start date: 2019-09-01, End date: 2024-08-31
Project acronym COORDSPACE
Project Chemistry of Coordination Space: Extraction, Storage, Activation and Catalysis
Researcher (PI) Martin Schroder
Host Institution (HI) THE UNIVERSITY OF NOTTINGHAM
Call Details Advanced Grant (AdG), PE5, ERC-2008-AdG
Summary The Applicant has an outstanding record of achievement and an international reputation for independent research across many areas of metal coordination chemistry. This high-impact and challenging Proposal brings together innovative ideas in coordination chemistry within a single inter- and multi-disciplinary project to open up new horizons across molecular and biological sciences, materials science and energy research. The Proposal applies coordination chemistry to the key issues of climate change, environmental and chemical sustainability, the Hydrogen Economy, carbon capture and fuel cell technologies, and atom-efficient metal extraction and clean-up. The vision is to bring together complementary areas and new applications of metal coordination chemistry and ligand design within an overarching and fundamental research program addressing: i. nanoscale functionalized framework polymers for the storage and activation of H2, CO2, CO, O2, N2, methane and volatile organic compounds; ii. new catalysts for the reversible oxidation and photochemical production of H2; iii) clean and selective recovery of precious metals (Pt, Pd, Rh, Ir, Hf, Zr) from process streams and ores. These research themes will be consolidated within a single cross-disciplinary and ambitious program focusing on the control of chemistry, reactivity and interactions within self-assembled confined and multi-functionalized space generated by designer porous framework materials. An AdG will afford the impetus and freedom via consolidated funding to undertake fundamental, speculative research with multiple potential big-hits across a wide range of disciplines. Via an extensive network of international academic and industrial collaborations, the Applicant will deliver major research breakthroughs in these vital areas, and train scientists for the future of Europe in an exciting, stimulating and curiosity-driven environment.
Summary
The Applicant has an outstanding record of achievement and an international reputation for independent research across many areas of metal coordination chemistry. This high-impact and challenging Proposal brings together innovative ideas in coordination chemistry within a single inter- and multi-disciplinary project to open up new horizons across molecular and biological sciences, materials science and energy research. The Proposal applies coordination chemistry to the key issues of climate change, environmental and chemical sustainability, the Hydrogen Economy, carbon capture and fuel cell technologies, and atom-efficient metal extraction and clean-up. The vision is to bring together complementary areas and new applications of metal coordination chemistry and ligand design within an overarching and fundamental research program addressing: i. nanoscale functionalized framework polymers for the storage and activation of H2, CO2, CO, O2, N2, methane and volatile organic compounds; ii. new catalysts for the reversible oxidation and photochemical production of H2; iii) clean and selective recovery of precious metals (Pt, Pd, Rh, Ir, Hf, Zr) from process streams and ores. These research themes will be consolidated within a single cross-disciplinary and ambitious program focusing on the control of chemistry, reactivity and interactions within self-assembled confined and multi-functionalized space generated by designer porous framework materials. An AdG will afford the impetus and freedom via consolidated funding to undertake fundamental, speculative research with multiple potential big-hits across a wide range of disciplines. Via an extensive network of international academic and industrial collaborations, the Applicant will deliver major research breakthroughs in these vital areas, and train scientists for the future of Europe in an exciting, stimulating and curiosity-driven environment.
Max ERC Funding
2 492 372 €
Duration
Start date: 2008-12-01, End date: 2013-11-30
Project acronym CORPLINK
Project Corporate Arbitrage and CPL Maps: Hidden Structures of Controls in the Global Economy
Researcher (PI) Ronen Peter Palan
Host Institution (HI) CITY UNIVERSITY OF LONDON
Call Details Advanced Grant (AdG), SH2, ERC-2015-AdG
Summary Political science conceptualises state-market relations as balancing acts between the public sphere (the state or government) and the private sphere (the market, dominated by large corporate bodies). The expansion of the global market has been led by the rise of large and highly mobile multinational firms. Since many of these companies command turnover comparable to the GDP of middle size states, globalisation is often seen as a global shift of power from states to markets, where corporate power stems from centralisation of resources, capital and structural influence over politics and society.
Yet over the past three decades, large firms have been strategically dividing themselves into hundreds and even thousands of multi-unit, multi-layered and multi-jurisdictional cells. Typically constructed to maximise flexibility and opportunity, such de-centring of the global firm over time has increased, not decreased, the power of the corporation in world politics, society and economy. Such practices amount to a new dimension of corporate power, arbitrage power, which is the main concept underpinning this project. Arbitrage power can be defined as the capacity of economic agents to capitalise on the gaps in the institutional and legal framework of the global economy. Traditional approaches to power analysis which conventionally prioritise individual agents or clusters of interests, are of limited help when engaging with the complex ecology of a de-centred firm.
CORPLINK has two aims: a) to develop a theoretical framework to study the processes of ‘arbitrage power’ as a distinct facet of economic power; b) to develop a novel transferable methodology for the investigation of corporate arbitrage power, CPL maps (Corporate Processes and Linkages maps). Specifically, the project innovates a new tool for the study of the firm as a political actor that navigates through complex networks and modalities of the global system of governance.
Summary
Political science conceptualises state-market relations as balancing acts between the public sphere (the state or government) and the private sphere (the market, dominated by large corporate bodies). The expansion of the global market has been led by the rise of large and highly mobile multinational firms. Since many of these companies command turnover comparable to the GDP of middle size states, globalisation is often seen as a global shift of power from states to markets, where corporate power stems from centralisation of resources, capital and structural influence over politics and society.
Yet over the past three decades, large firms have been strategically dividing themselves into hundreds and even thousands of multi-unit, multi-layered and multi-jurisdictional cells. Typically constructed to maximise flexibility and opportunity, such de-centring of the global firm over time has increased, not decreased, the power of the corporation in world politics, society and economy. Such practices amount to a new dimension of corporate power, arbitrage power, which is the main concept underpinning this project. Arbitrage power can be defined as the capacity of economic agents to capitalise on the gaps in the institutional and legal framework of the global economy. Traditional approaches to power analysis which conventionally prioritise individual agents or clusters of interests, are of limited help when engaging with the complex ecology of a de-centred firm.
CORPLINK has two aims: a) to develop a theoretical framework to study the processes of ‘arbitrage power’ as a distinct facet of economic power; b) to develop a novel transferable methodology for the investigation of corporate arbitrage power, CPL maps (Corporate Processes and Linkages maps). Specifically, the project innovates a new tool for the study of the firm as a political actor that navigates through complex networks and modalities of the global system of governance.
Max ERC Funding
1 739 387 €
Duration
Start date: 2016-12-01, End date: 2020-11-30
Project acronym COSMOS
Project Control and measurement of single macromolecules in space and time
Researcher (PI) Madhavi KRISHNAN
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Consolidator Grant (CoG), PE4, ERC-2016-COG
Summary The desire to “freely suspend the constituents of matter” in order to study their behaviour can be traced back over 200 years to Lichtenberg’s diaries. From radio-frequency ion traps to optical tweezing of colloidal particles, existing methods to trap matter in free space or solution rely on the use of external fields that often strongly perturb the integrity of a macromolecule in solution. Recently, I invented the ‘electrostatic fluidic trap’, a “field-free” principle that supports stable, non-destructive confinement of single macromolecules in room temperature fluids, representing a paradigm shift in a nearly century-old field. The spatio-temporal dynamics of a single electrostatically trapped molecule reveals fundamental information on its properties, e.g., size and electrical charge. The charge of a macromolecule is in turn a strong function of its 3D conformation - the molecular basis of biological function. I now aim to develop a new platform to study 3D macromolecular structure and temporal conformation by measuring the electrical charge of a single trapped molecule in real time, using both optical microscopy and electrical detection. Beyond the conformational dynamics of a single molecule, we will also examine interactions between two or more molecules, and the detection of minute structural differences between closely related molecular isoforms. We will further develop a novel approach to electrical transport measurements on single molecules aimed at generating for the first time a catalog of ‘electrical signatures’ for biomolecules in solution. The ability to experimentally link electrical charge and molecular structure will not only open up a new physical dimension in our understanding of macromolecules, but also advance the development of ultrasensitive, high-throughput molecular sensors for biomedical detection and analytics, potentially enabling an optical or electrical “single-snapshot” read-out of the proteome or transcriptome of a single cell.
Summary
The desire to “freely suspend the constituents of matter” in order to study their behaviour can be traced back over 200 years to Lichtenberg’s diaries. From radio-frequency ion traps to optical tweezing of colloidal particles, existing methods to trap matter in free space or solution rely on the use of external fields that often strongly perturb the integrity of a macromolecule in solution. Recently, I invented the ‘electrostatic fluidic trap’, a “field-free” principle that supports stable, non-destructive confinement of single macromolecules in room temperature fluids, representing a paradigm shift in a nearly century-old field. The spatio-temporal dynamics of a single electrostatically trapped molecule reveals fundamental information on its properties, e.g., size and electrical charge. The charge of a macromolecule is in turn a strong function of its 3D conformation - the molecular basis of biological function. I now aim to develop a new platform to study 3D macromolecular structure and temporal conformation by measuring the electrical charge of a single trapped molecule in real time, using both optical microscopy and electrical detection. Beyond the conformational dynamics of a single molecule, we will also examine interactions between two or more molecules, and the detection of minute structural differences between closely related molecular isoforms. We will further develop a novel approach to electrical transport measurements on single molecules aimed at generating for the first time a catalog of ‘electrical signatures’ for biomolecules in solution. The ability to experimentally link electrical charge and molecular structure will not only open up a new physical dimension in our understanding of macromolecules, but also advance the development of ultrasensitive, high-throughput molecular sensors for biomedical detection and analytics, potentially enabling an optical or electrical “single-snapshot” read-out of the proteome or transcriptome of a single cell.
Max ERC Funding
2 124 965 €
Duration
Start date: 2018-06-01, End date: 2023-05-31
Project acronym CoSuN
Project Cooperative Phenomena in Supramolecular Nanostructures
Researcher (PI) Harry Laurence Anderson
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Advanced Grant (AdG), PE5, ERC-2012-ADG_20120216
Summary Many of the remarkable properties of molecular nanostructures are cooperative effects. A system is described as cooperative when it behaves differently from expectations based on the properties of its individual components. Multivalent cooperativity is crucial for biological molecular recognition, yet the factors determining the magnitude of this effect are poorly understood. Excitonic cooperativity is exploited in sensitive detectors for explosives, and is the basis of photosynthetic light harvesting. Electronic cooperativity is illustrated on the molecular scale by the phenomenon of aromaticity, and on a larger scale by metallic conductivity. Magnetic properties provide many examples of cooperativity. The magnitude of cooperative effects increases with the strength of coupling between the individual components, and with the number of coupled components. Cooperative systems exhibit sharp changes in behavior in response to small changes in conditions, such as transitions from free to bound, fluorescent to non-fluorescent, or conductive to insulating. The tendency towards an “all-or-nothing” response is often useful; in the limit of a very large ensemble, it leads to phase transitions. The CoSuN project will extend methodology developed in Oxford to create large monodisperse supramolecular nanostructures which are uniquely suited for exploring multivalent, excitonic and electronic cooperativity. The template-directed synthesis of these nanostructures is made possible by strong multivalent cooperativity, while the electronic coupling between the individual subunits results in other cooperative phenomena. This project will clarify understanding of cooperative molecular recognition. It will also help to solve some of the mysteries of photosynthesis and reveal the first molecular manifestations of coherent quantum mechanical phenomena, such as Aharonov-Bohm effects.
Summary
Many of the remarkable properties of molecular nanostructures are cooperative effects. A system is described as cooperative when it behaves differently from expectations based on the properties of its individual components. Multivalent cooperativity is crucial for biological molecular recognition, yet the factors determining the magnitude of this effect are poorly understood. Excitonic cooperativity is exploited in sensitive detectors for explosives, and is the basis of photosynthetic light harvesting. Electronic cooperativity is illustrated on the molecular scale by the phenomenon of aromaticity, and on a larger scale by metallic conductivity. Magnetic properties provide many examples of cooperativity. The magnitude of cooperative effects increases with the strength of coupling between the individual components, and with the number of coupled components. Cooperative systems exhibit sharp changes in behavior in response to small changes in conditions, such as transitions from free to bound, fluorescent to non-fluorescent, or conductive to insulating. The tendency towards an “all-or-nothing” response is often useful; in the limit of a very large ensemble, it leads to phase transitions. The CoSuN project will extend methodology developed in Oxford to create large monodisperse supramolecular nanostructures which are uniquely suited for exploring multivalent, excitonic and electronic cooperativity. The template-directed synthesis of these nanostructures is made possible by strong multivalent cooperativity, while the electronic coupling between the individual subunits results in other cooperative phenomena. This project will clarify understanding of cooperative molecular recognition. It will also help to solve some of the mysteries of photosynthesis and reveal the first molecular manifestations of coherent quantum mechanical phenomena, such as Aharonov-Bohm effects.
Max ERC Funding
2 452 688 €
Duration
Start date: 2013-05-01, End date: 2018-04-30
Project acronym CPFTMW
Project New Applications of Broadband Rotational Spectroscopy
Researcher (PI) Nicholas Walker
Host Institution (HI) UNIVERSITY OF NEWCASTLE UPON TYNE
Call Details Starting Grant (StG), PE4, ERC-2012-StG_20111012
Summary "The recent invention of the chirped-pulse, Fourier transform microwave (CP-FTMW) spectrometer will allow application of rotational spectroscopy to a greatly expanded range of challenges over the next decade. The proposed work will apply the state-of-the-art CP-FTMW spectrometer at the University of Bristol to major themes in both fundamental and applied research. Palladium, platinum and nickel catalysts are of central importance in synthetic chemistry and the industrial production of chemicals. The microwave spectra of Mn...(C2H4), Mn...(C2H2), Mn-CCH and Mn-CH2 (M= Ni, Pd or Pt, n=1-3) will be measured to characterise structural and other changes induced in C2H4 and C2H2 by attachment to these metals. The results will inform understanding of the mechanisms of catalysis. The role and function of metal ions will be another major theme of the programme. Infrared-microwave (IR-MW) double resonance will be used to determine structures for (H2O)n...MCl and (H2O)n...MF (where M=Cu, Ag or Au and n=1-6) to gain insight into the interactions that govern solvation shell formation. Copper ions have biological significance and govern the conformations adopted by proteins that include amyloid B-peptide, the production of which is associated with Alzheimer’s disease and cytochrome C oxidase which is important for respiration. IR-MW double resonance will be used to probe the structure of complexes where the ionic copper atom of a copper chloride molecule coordinates to glycine, imidazole, alanine, histidine and cysteine, respectively. The proposed work will provide precise data for modelling of interactions in protein active sites. Finally, technical innovations will be implemented to support applications of the instrument in chemical analysis. A GC-CP-FTMW (GC=gas chromatography) instrument will be constructed to allow analysis of the composition of wine and fruit juice with the aim of establishing CP-FTMW spectroscopy as a useful tool for commercial applications."
Summary
"The recent invention of the chirped-pulse, Fourier transform microwave (CP-FTMW) spectrometer will allow application of rotational spectroscopy to a greatly expanded range of challenges over the next decade. The proposed work will apply the state-of-the-art CP-FTMW spectrometer at the University of Bristol to major themes in both fundamental and applied research. Palladium, platinum and nickel catalysts are of central importance in synthetic chemistry and the industrial production of chemicals. The microwave spectra of Mn...(C2H4), Mn...(C2H2), Mn-CCH and Mn-CH2 (M= Ni, Pd or Pt, n=1-3) will be measured to characterise structural and other changes induced in C2H4 and C2H2 by attachment to these metals. The results will inform understanding of the mechanisms of catalysis. The role and function of metal ions will be another major theme of the programme. Infrared-microwave (IR-MW) double resonance will be used to determine structures for (H2O)n...MCl and (H2O)n...MF (where M=Cu, Ag or Au and n=1-6) to gain insight into the interactions that govern solvation shell formation. Copper ions have biological significance and govern the conformations adopted by proteins that include amyloid B-peptide, the production of which is associated with Alzheimer’s disease and cytochrome C oxidase which is important for respiration. IR-MW double resonance will be used to probe the structure of complexes where the ionic copper atom of a copper chloride molecule coordinates to glycine, imidazole, alanine, histidine and cysteine, respectively. The proposed work will provide precise data for modelling of interactions in protein active sites. Finally, technical innovations will be implemented to support applications of the instrument in chemical analysis. A GC-CP-FTMW (GC=gas chromatography) instrument will be constructed to allow analysis of the composition of wine and fruit juice with the aim of establishing CP-FTMW spectroscopy as a useful tool for commercial applications."
Max ERC Funding
1 497 862 €
Duration
Start date: 2012-11-01, End date: 2017-10-31
Project acronym CRYOMAT
Project Antifreeze GlycoProtein Mimetic Polymers
Researcher (PI) Matthew Ian Gibson
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Starting Grant (StG), PE5, ERC-2014-STG
Summary Fish living in polar oceans have evolved an elegant, macromolecular, solution to survive in sub-zero water: they secrete antifreeze (glyco)proteins (AFGPs) which have several ‘antifreeze’ effects, including ice recrystallization inhibition (IRI) - they slow the rate of ice crystal growth. Ice crystal growth is a major problem in settings as diverse as oil fields, wind turbines, road surfaces and frozen food. Analysis of the process of cryopreservation, whereby donor cells are frozen for later use, has revealed that ice recrystallization is a major contributor to cell death upon thawing. Enhanced cryopreservation methods are particularly needed for stem cell storage to maximize the use of this currently limited resource, but also to enable storage of clinically transfused cells such as platelets and red blood cells. AFGPs have thus far not found application in cryopreservation due to their low availability from natural sources, extremely challenging synthesis, indications of cytotoxicity, but more importantly they have a side effect of shaping ice crystals into needle-shapes which pierces cells’ membranes, killing them. The aim of this ambitious project is to take a multidisciplinary approach to develop synthetic polymers as tunable, scalable and accessible bio-mimetics of AFGPs, which specifically reproduce only the desirable IRI properties. Precision synthetic and biological methods will be applied to access both vinyl- and peptide- based materials with IRI activity. The bio-inspired approach taken here will include detailed biophysical analysis of the polymer-ice interactions and translation of this understanding to real cryopreservation scenarios using blood-borne cells and human stem cells. In summary, this ambitious project takes inspiration from Nature's defense mechanisms that have evolved to allow life to flourish in extreme environments and will employ modern polymer chemistry to apply it to a real clinical problem; cryopreservation.
Summary
Fish living in polar oceans have evolved an elegant, macromolecular, solution to survive in sub-zero water: they secrete antifreeze (glyco)proteins (AFGPs) which have several ‘antifreeze’ effects, including ice recrystallization inhibition (IRI) - they slow the rate of ice crystal growth. Ice crystal growth is a major problem in settings as diverse as oil fields, wind turbines, road surfaces and frozen food. Analysis of the process of cryopreservation, whereby donor cells are frozen for later use, has revealed that ice recrystallization is a major contributor to cell death upon thawing. Enhanced cryopreservation methods are particularly needed for stem cell storage to maximize the use of this currently limited resource, but also to enable storage of clinically transfused cells such as platelets and red blood cells. AFGPs have thus far not found application in cryopreservation due to their low availability from natural sources, extremely challenging synthesis, indications of cytotoxicity, but more importantly they have a side effect of shaping ice crystals into needle-shapes which pierces cells’ membranes, killing them. The aim of this ambitious project is to take a multidisciplinary approach to develop synthetic polymers as tunable, scalable and accessible bio-mimetics of AFGPs, which specifically reproduce only the desirable IRI properties. Precision synthetic and biological methods will be applied to access both vinyl- and peptide- based materials with IRI activity. The bio-inspired approach taken here will include detailed biophysical analysis of the polymer-ice interactions and translation of this understanding to real cryopreservation scenarios using blood-borne cells and human stem cells. In summary, this ambitious project takes inspiration from Nature's defense mechanisms that have evolved to allow life to flourish in extreme environments and will employ modern polymer chemistry to apply it to a real clinical problem; cryopreservation.
Max ERC Funding
1 496 439 €
Duration
Start date: 2015-06-01, End date: 2020-05-31
Project acronym CSI.interface
Project A molecular interface science approach: Decoding single molecular reactions and interactions at dynamic solid/liquid interfaces
Researcher (PI) Markus Valtiner
Host Institution (HI) TECHNISCHE UNIVERSITAET WIEN
Call Details Starting Grant (StG), PE4, ERC-2015-STG
Summary After decades of truly transformative advancements in single molecule (bio)physics and surface science, it is still no more than a vision to predict and control macroscopic phenomena such as adhesion or electrochemical reaction rates at solid/liquid interfaces based on well-characterized single molecular interactions. How exactly do inherently dynamic and simultaneous interactions of a countless number of interacting “crowded” molecules lead to a concerted outcome/property on a macroscopic scale?
Here, I propose a unique approach that will allow us to unravel the scaling of single molecule interactions towards macroscopic properties at adhesive and redox-active solid/liquid interfaces. Combining Atomic Force Microscopy (AFM) based single molecule force spectroscopy and macroscopic Surface Forces Apparatus (SFA) experiments CSI.interface will (1) derive rules for describing nonlinearities observed in complex, crowded (water and ions) and chemically diverse adhesive solid/liquid interfaces; (2) uniquely characterize all relevant kinetic parameters (interaction free energy and transition states) of electrochemical and adhesive reactions/interactions of single molecules at chemically defined surfaces as well as electrified single crystal facets and step edges. Complementary, (3) my team and I will build a novel molecular force apparatus in order to measure single-molecule steady-state dynamics of both redox cycles as well as binding unbinding cycles of specific interactions, and how these react to environmental triggers.
CSI.interface goes well beyond present applications of AFM and SFA and has the long-term potential to revolutionize our understanding of interfacial interaction under steady state, responsive and dynamic conditions. This work will pave the road for knowledge based designing of next-generation technologies in gluing, coating, bio-adhesion, materials design and much beyond.
Summary
After decades of truly transformative advancements in single molecule (bio)physics and surface science, it is still no more than a vision to predict and control macroscopic phenomena such as adhesion or electrochemical reaction rates at solid/liquid interfaces based on well-characterized single molecular interactions. How exactly do inherently dynamic and simultaneous interactions of a countless number of interacting “crowded” molecules lead to a concerted outcome/property on a macroscopic scale?
Here, I propose a unique approach that will allow us to unravel the scaling of single molecule interactions towards macroscopic properties at adhesive and redox-active solid/liquid interfaces. Combining Atomic Force Microscopy (AFM) based single molecule force spectroscopy and macroscopic Surface Forces Apparatus (SFA) experiments CSI.interface will (1) derive rules for describing nonlinearities observed in complex, crowded (water and ions) and chemically diverse adhesive solid/liquid interfaces; (2) uniquely characterize all relevant kinetic parameters (interaction free energy and transition states) of electrochemical and adhesive reactions/interactions of single molecules at chemically defined surfaces as well as electrified single crystal facets and step edges. Complementary, (3) my team and I will build a novel molecular force apparatus in order to measure single-molecule steady-state dynamics of both redox cycles as well as binding unbinding cycles of specific interactions, and how these react to environmental triggers.
CSI.interface goes well beyond present applications of AFM and SFA and has the long-term potential to revolutionize our understanding of interfacial interaction under steady state, responsive and dynamic conditions. This work will pave the road for knowledge based designing of next-generation technologies in gluing, coating, bio-adhesion, materials design and much beyond.
Max ERC Funding
1 499 750 €
Duration
Start date: 2016-07-01, End date: 2021-06-30
Project acronym CSIASC
Project Changing Structures of Islamic Authority and Consequences for Social Change: A Transnational Review
Researcher (PI) Masooda Bano
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), SH2, ERC-2013-StG
Summary Research on Muslims in Europe or in the Muslim majority countries has since September 11, mainly focused on understanding the causes of religious radicalization. Largely ignored in the public debates, as well as in academic scholarship, is recognition of the rapid growth in a number of prominent initiatives emerging within Muslims in the west that are aimed at initiating intellectual revival within Islam. Drawing inspiration from the thinkers such as Al-Ghazali or Ibn-Rushd (associated with the ‘rationalist tradition’ in Islam), the Muslim intellectuals and scholars at the center of this movement for intellectual revival in Islam are arguing for ‘indigenizing Islam in the West.’ This project is aimed at understanding the emergence and growth of this movement, the methodology different actors within this movement adopt to initiate reform while remaining loyal to the Islamic ethical spirit, and the implications of these attempts at intellectual reform for individual behavior and social change within Muslims in the west as well as in Muslim majority countries. The project will situate the emergence of this movement within the broader shifts being witnessed in the traditional structures of Islamic authority— such as Al-Azhar University, Dar-ul Uloom, Deoband, Diyanat, and Al-Medina University— that dominate the teaching and interpretation of Islam globally but are under pressure to reform. By developing detailed ethnographic accounts of these new and old institutions of Islamic authority, examining the intellectual discourse of their scholars, observing the argumentations through which they socially advance their conception of Islam, and analyzing how these discourses impact real life choices, this project will shed light on the complexity of Islamic thought and changes in contemporary Muslim societies. It will also highlight the spaces that are emerging for engagement between the Islamic and western tradition and inform theory of religious behavior.
Summary
Research on Muslims in Europe or in the Muslim majority countries has since September 11, mainly focused on understanding the causes of religious radicalization. Largely ignored in the public debates, as well as in academic scholarship, is recognition of the rapid growth in a number of prominent initiatives emerging within Muslims in the west that are aimed at initiating intellectual revival within Islam. Drawing inspiration from the thinkers such as Al-Ghazali or Ibn-Rushd (associated with the ‘rationalist tradition’ in Islam), the Muslim intellectuals and scholars at the center of this movement for intellectual revival in Islam are arguing for ‘indigenizing Islam in the West.’ This project is aimed at understanding the emergence and growth of this movement, the methodology different actors within this movement adopt to initiate reform while remaining loyal to the Islamic ethical spirit, and the implications of these attempts at intellectual reform for individual behavior and social change within Muslims in the west as well as in Muslim majority countries. The project will situate the emergence of this movement within the broader shifts being witnessed in the traditional structures of Islamic authority— such as Al-Azhar University, Dar-ul Uloom, Deoband, Diyanat, and Al-Medina University— that dominate the teaching and interpretation of Islam globally but are under pressure to reform. By developing detailed ethnographic accounts of these new and old institutions of Islamic authority, examining the intellectual discourse of their scholars, observing the argumentations through which they socially advance their conception of Islam, and analyzing how these discourses impact real life choices, this project will shed light on the complexity of Islamic thought and changes in contemporary Muslim societies. It will also highlight the spaces that are emerging for engagement between the Islamic and western tradition and inform theory of religious behavior.
Max ERC Funding
1 376 704 €
Duration
Start date: 2014-03-01, End date: 2019-12-31
Project acronym CSRS
Project A Comparative Study of Resilience in Survivors of War Rape and Sexual Violence: New Directions for Transitional Justice
Researcher (PI) Janine Clark
Host Institution (HI) THE UNIVERSITY OF BIRMINGHAM
Call Details Consolidator Grant (CoG), SH2, ERC-2016-COG
Summary The profound trauma associated with rape and sexual violence in conflict has been extensively explored within existing scholarship. The fact that many survivors exhibit remarkable post-trauma resilience, however, remains critically under-investigated. CSRS will address this fundamental gap by undertaking a paradigm-shifting empirical study of the underlying conditions for resilience. It will then use this data to pioneer a new, survivor-centred model of transitional justice – the process of redressing the legacy of massive human rights abuses.
Using the three comparative case studies of Bosnia-Hercegovina (BiH), the Democratic Republic of Congo (DRC) and Colombia, and adopting a social-ecological approach that emphasizes the interactions between individuals and their environments, CSRS consists of two inter-linked parts. The first part will involve extensive fieldwork, using a combination of quantitative and qualitative research methods, to generate a rich cross-cultural dataset that identifies and explains the key micro, meso and macro factors that foster resilience in survivors of war rape and sexual violence.
The second part of CSRS will use this dataset to build an innovative, bottom-up model of transitional justice that prioritizes the long-term needs of survivors, reflecting the project’s hypothesis that a positive correlation exists between fulfilment of needs and resilience. This model will be developed with the input of survivors in BiH, the DRC and Colombia and in consultation with transitional justice scholars and practitioners. CSRS aims to transform transitional justice theory and practice. The project outputs will therefore include both academic publications and policy reports to communicate the model to the governments of the case study countries, the United Nations and a wider international audience with the overall aim of making empowerment and resilience part of a new transitional justice agenda.
Summary
The profound trauma associated with rape and sexual violence in conflict has been extensively explored within existing scholarship. The fact that many survivors exhibit remarkable post-trauma resilience, however, remains critically under-investigated. CSRS will address this fundamental gap by undertaking a paradigm-shifting empirical study of the underlying conditions for resilience. It will then use this data to pioneer a new, survivor-centred model of transitional justice – the process of redressing the legacy of massive human rights abuses.
Using the three comparative case studies of Bosnia-Hercegovina (BiH), the Democratic Republic of Congo (DRC) and Colombia, and adopting a social-ecological approach that emphasizes the interactions between individuals and their environments, CSRS consists of two inter-linked parts. The first part will involve extensive fieldwork, using a combination of quantitative and qualitative research methods, to generate a rich cross-cultural dataset that identifies and explains the key micro, meso and macro factors that foster resilience in survivors of war rape and sexual violence.
The second part of CSRS will use this dataset to build an innovative, bottom-up model of transitional justice that prioritizes the long-term needs of survivors, reflecting the project’s hypothesis that a positive correlation exists between fulfilment of needs and resilience. This model will be developed with the input of survivors in BiH, the DRC and Colombia and in consultation with transitional justice scholars and practitioners. CSRS aims to transform transitional justice theory and practice. The project outputs will therefore include both academic publications and policy reports to communicate the model to the governments of the case study countries, the United Nations and a wider international audience with the overall aim of making empowerment and resilience part of a new transitional justice agenda.
Max ERC Funding
1 790 580 €
Duration
Start date: 2017-09-01, End date: 2022-08-31
Project acronym CSV
Project "Conflict, Strategies, and Violence: An Actor-based Approach to Violent and Non-Violent Interactions"
Researcher (PI) Kristian Skrede Gleditsch
Host Institution (HI) UNIVERSITY OF ESSEX
Call Details Starting Grant (StG), SH2, ERC-2012-StG_20111124
Summary "Existing research has tended to equate conflict with violence, lumping all “non-conflict” situations together. This is unfortunate on theoretical and empirical grounds. Definitions of conflict highlight incompatibilities, which may motivate actors to resort to violence, but do not automatically generate violence and can be settled or managed in non-violent ways. Lumping together as “not violence” both cases without incompatibilities or agency and cases where actors pursue different strategies ultimately undermines our ability to understand conflict processes and test core arguments about conflict, strategies, and violence, and leaves us unable to assess whether the observed global decline in violence may reflect increasing use of alternative strategies, more state deterrence/accommodation, or fewer incompatibilities in the first place. This project will examine conflict in terms of incompatibilities between actors, where the specific structure of the incompatibilities and the strategies and interactions determine whether we see escalation to violence as well as alternative outcomes such as accommodation or regime change. It will extend my prior research on civil war and focus more clearly on actor motivations, alternative outcomes to conventional civil war, and take seriously non-violent strategies in conflict and protest. Whereas previous research has tended to study violent and non-violent conflict as separate phenomena, this project will focus on violent and non-violent actions as possible substitutes and compliment and explain variation across a range of alternative outcomes, as illustrated in the so-called Arab spring, where we see both non-violent protest and violent insurgencies, as well as state responses ranging from violent repression to accommodation. The project will also consider how transnational factors can influence the choice of strategies that actors make in conflicts."
Summary
"Existing research has tended to equate conflict with violence, lumping all “non-conflict” situations together. This is unfortunate on theoretical and empirical grounds. Definitions of conflict highlight incompatibilities, which may motivate actors to resort to violence, but do not automatically generate violence and can be settled or managed in non-violent ways. Lumping together as “not violence” both cases without incompatibilities or agency and cases where actors pursue different strategies ultimately undermines our ability to understand conflict processes and test core arguments about conflict, strategies, and violence, and leaves us unable to assess whether the observed global decline in violence may reflect increasing use of alternative strategies, more state deterrence/accommodation, or fewer incompatibilities in the first place. This project will examine conflict in terms of incompatibilities between actors, where the specific structure of the incompatibilities and the strategies and interactions determine whether we see escalation to violence as well as alternative outcomes such as accommodation or regime change. It will extend my prior research on civil war and focus more clearly on actor motivations, alternative outcomes to conventional civil war, and take seriously non-violent strategies in conflict and protest. Whereas previous research has tended to study violent and non-violent conflict as separate phenomena, this project will focus on violent and non-violent actions as possible substitutes and compliment and explain variation across a range of alternative outcomes, as illustrated in the so-called Arab spring, where we see both non-violent protest and violent insurgencies, as well as state responses ranging from violent repression to accommodation. The project will also consider how transnational factors can influence the choice of strategies that actors make in conflicts."
Max ERC Funding
1 174 476 €
Duration
Start date: 2013-02-01, End date: 2018-01-31
Project acronym CytoChem
Project A Chemical Approach to Understanding Cell Division
Researcher (PI) Ulrike Sophie Eggert
Host Institution (HI) KING'S COLLEGE LONDON
Call Details Starting Grant (StG), PE5, ERC-2012-StG_20111012
Summary Many mechanisms underlying cytokinesis, the final step in cell division, remain poorly understood. The goal of my laboratory is to use chemical biology approaches to address some of the unanswered mechanistic questions by studying cytokinesis at the process, pathway and protein levels. I aim to discover small molecules that specifically target cytokinesis by different mechanisms because they are important tools to study the biology of cell division and could catalyze the discovery of therapeutics.
I am proposing here to use small molecules we discovered to study how the Rho pathway regulates cytokinesis. We will synthesize focused libraries around selected compounds to optimize their properties and to identify sites for affinity tags. I am proposing to identify our small molecules’ cellular targets using a combination of approaches, including a new strategy I designed that takes advantage of the fact that they target a discrete signalling pathway.
Rho signalling is involved in every step of cytokinesis, but there are many outstanding questions about how this occurs and which proteins are involved. We have completed a genome-wide RNAi screen that has revealed the identity of new proteins connected to Rho signalling. We will combine functional investigations into how these proteins participate in cytokinesis with our newly discovered small molecules. With this array of tools in hand, we expect to use imaging and other cell-based assays to gain of comprehensive understanding of the role of Rho signalling during cytokinesis and other Rho-dependent processes.
Summary
Many mechanisms underlying cytokinesis, the final step in cell division, remain poorly understood. The goal of my laboratory is to use chemical biology approaches to address some of the unanswered mechanistic questions by studying cytokinesis at the process, pathway and protein levels. I aim to discover small molecules that specifically target cytokinesis by different mechanisms because they are important tools to study the biology of cell division and could catalyze the discovery of therapeutics.
I am proposing here to use small molecules we discovered to study how the Rho pathway regulates cytokinesis. We will synthesize focused libraries around selected compounds to optimize their properties and to identify sites for affinity tags. I am proposing to identify our small molecules’ cellular targets using a combination of approaches, including a new strategy I designed that takes advantage of the fact that they target a discrete signalling pathway.
Rho signalling is involved in every step of cytokinesis, but there are many outstanding questions about how this occurs and which proteins are involved. We have completed a genome-wide RNAi screen that has revealed the identity of new proteins connected to Rho signalling. We will combine functional investigations into how these proteins participate in cytokinesis with our newly discovered small molecules. With this array of tools in hand, we expect to use imaging and other cell-based assays to gain of comprehensive understanding of the role of Rho signalling during cytokinesis and other Rho-dependent processes.
Max ERC Funding
1 499 080 €
Duration
Start date: 2012-10-01, End date: 2017-09-30
Project acronym DEBIDEM
Project Defining Belief and Identities in the Eastern Mediterranean:
The Role of Interreligious Debate and Interaction
Researcher (PI) Ioannis Papadogiannakis
Host Institution (HI) KING'S COLLEGE LONDON
Call Details Starting Grant (StG), SH2, ERC-2010-StG_20091209
Summary This project seeks to recover the processes by which religious beliefs and identities were defined through interreligious interaction and debate in the religious culture of a broader social base in the eastern Mediterranean (6-8th centuries AD) through examination of a neglected, unconventional corpus of medieval Greek, Syriac and Arabic literature of debate and disputation (consisting of collections of questions and answers, dialogues among others), treating authors such as Ps. Kaisarios, Anastasios of Sinai, and Ps. Athanasios. These sources help us to understand the kinds of perplexities that were being raised in Christian communities of the eastern Mediterranean as they negotiated a lively and contentious religious and social landscape, and they highlight the multifarious issues which Christian leaders had to be prepared to deal with in their pastoral, pedagogical, and apologetic work. At the same time these collections must be seen as an attempt by Christian authors to work out how Christianity was to define its position with regard to other religions (Hellenism, Judaism and Islam) in a period still characterized by considerable fluidity and change.
As well as writing those doubts, challenges, objections, concerns, issues and anxieties back into the religious history of the eastern Mediterranean, when completed this full-length study of these texts will provide scholars not only with a detailed knowledge of the ways in which religious belief, practice and communities were defined in contrast to other religious systems, and a fuller sense of the religious, social and intellectual history of the eastern Mediterranean but also with a nuanced picture of their self-definition, one which will be more sensitive to the processes that led to its formation.
Summary
This project seeks to recover the processes by which religious beliefs and identities were defined through interreligious interaction and debate in the religious culture of a broader social base in the eastern Mediterranean (6-8th centuries AD) through examination of a neglected, unconventional corpus of medieval Greek, Syriac and Arabic literature of debate and disputation (consisting of collections of questions and answers, dialogues among others), treating authors such as Ps. Kaisarios, Anastasios of Sinai, and Ps. Athanasios. These sources help us to understand the kinds of perplexities that were being raised in Christian communities of the eastern Mediterranean as they negotiated a lively and contentious religious and social landscape, and they highlight the multifarious issues which Christian leaders had to be prepared to deal with in their pastoral, pedagogical, and apologetic work. At the same time these collections must be seen as an attempt by Christian authors to work out how Christianity was to define its position with regard to other religions (Hellenism, Judaism and Islam) in a period still characterized by considerable fluidity and change.
As well as writing those doubts, challenges, objections, concerns, issues and anxieties back into the religious history of the eastern Mediterranean, when completed this full-length study of these texts will provide scholars not only with a detailed knowledge of the ways in which religious belief, practice and communities were defined in contrast to other religious systems, and a fuller sense of the religious, social and intellectual history of the eastern Mediterranean but also with a nuanced picture of their self-definition, one which will be more sensitive to the processes that led to its formation.
Max ERC Funding
1 483 119 €
Duration
Start date: 2011-01-01, End date: 2016-12-31
Project acronym DEBUNKER
Project The Problem of European Misperceptions in Politics, Health, and Science:Causes, Consequences, and the Search for Solutions
Researcher (PI) Jason Aaron Reifler
Host Institution (HI) THE UNIVERSITY OF EXETER
Call Details Consolidator Grant (CoG), SH2, ERC-2015-CoG
Summary While some people may simply lack relevant factual knowledge, others may actively hold incorrect beliefs. These factual beliefs that are not supported by clear evidence and expert opinion are what scholars call misperceptions (Nyhan and Reifler 2010). This project is principally about misperceptions—the “facts” that people believe that simply are not true. What misperceptions do Europeans hold on issues like immigration, vaccines, and climate change? Who holds these misperceptions? What demographic and attitudinal variables are correlated with holding misperceptions? And ultimately, what can be done to help reduce misperceptions?
Misperceptions are an important topic for study because they distort public preferences and outcomes. This research program investigating misperceptions is currently at the state of the art in political science. To date, only a handful of published studies by political scientists have examined how corrective information changes underlying factual beliefs. The results of these studies are uniformly troubling—among those vulnerable to holding a given misperception, corrective efforts often make misperceptions worse or decrease the likelihood to engage in desired behaviors.
This ambitious project has three primary objectives. First, the project will assess levels of misperceptions in Europe on three specific issues (immigration, vaccines, and climate change) that represent three different substantive domains of knowledge (politics, health, and science). Second, the project will examine a variety of approaches and techniques for combatting misperceptions and generating effective corrections. Third, the project will take what is learned from the first two stages and transmit the findings back to relevant academic and policy-maker audiences in order to aid policy design and communication efforts on important policy issues.
Summary
While some people may simply lack relevant factual knowledge, others may actively hold incorrect beliefs. These factual beliefs that are not supported by clear evidence and expert opinion are what scholars call misperceptions (Nyhan and Reifler 2010). This project is principally about misperceptions—the “facts” that people believe that simply are not true. What misperceptions do Europeans hold on issues like immigration, vaccines, and climate change? Who holds these misperceptions? What demographic and attitudinal variables are correlated with holding misperceptions? And ultimately, what can be done to help reduce misperceptions?
Misperceptions are an important topic for study because they distort public preferences and outcomes. This research program investigating misperceptions is currently at the state of the art in political science. To date, only a handful of published studies by political scientists have examined how corrective information changes underlying factual beliefs. The results of these studies are uniformly troubling—among those vulnerable to holding a given misperception, corrective efforts often make misperceptions worse or decrease the likelihood to engage in desired behaviors.
This ambitious project has three primary objectives. First, the project will assess levels of misperceptions in Europe on three specific issues (immigration, vaccines, and climate change) that represent three different substantive domains of knowledge (politics, health, and science). Second, the project will examine a variety of approaches and techniques for combatting misperceptions and generating effective corrections. Third, the project will take what is learned from the first two stages and transmit the findings back to relevant academic and policy-maker audiences in order to aid policy design and communication efforts on important policy issues.
Max ERC Funding
1 931 730 €
Duration
Start date: 2016-09-01, End date: 2021-08-31
Project acronym DeCO-HVP
Project Decouple Electrochemical Reduction of Carbon Dioxide to High Value Products
Researcher (PI) Kathryn Ellen TOGHILL
Host Institution (HI) UNIVERSITY OF LANCASTER
Call Details Starting Grant (StG), PE4, ERC-2018-STG
Summary This programme aims to convert carbon dioxide into high value hydrocarbon products using carbon neutral electrochemical methods. High value products are materials that may be used as carbon based chemical feedstocks and as synthetic fuels, reducing the ever-present demand on oil and natural gas to fulfil these needs. The project is within the remit of an international ambition to valorise carbon dioxide waste and reduce environmentally harmful greenhouse gas generation, as opposed to stopping at carbon capture and sequestration. This proposal outlines an alternative route to carbon dioxide utilisation (CDU), in which a mediated approach that decouples the electrochemical reduction from the catalytic process is explored. Novel bimetallic catalysts will be synthesised and studied, meditating electron donating solutions will be generated, and a robust and comprehensive analytical arrangement will be implemented to allow total identification and quantification of the wide range of possible products.
Electrocatalytic CO2 reduction is one of the key approaches to CDU, as it has a direct pathway to carbon neutral renewable electricity. Nonetheless it is a field that has shown minimal progress in the past 30 years. A paradigm shift is necessary in the approach to electrochemical CO2 reduction, where conventional heterogeneous interfacial catalysis is limited by mass transport, passivation, and CO2 solubility. This proposal outlines the use of electron donating mediators generated separately to the catalysed chemical reduction of CO2, such that the electrolyte becomes the electrode. This opens a whole new avenue for catalyst research, and here target bimetallic catalysts that suppress side reactions and promote high value product synthesis are described.
Summary
This programme aims to convert carbon dioxide into high value hydrocarbon products using carbon neutral electrochemical methods. High value products are materials that may be used as carbon based chemical feedstocks and as synthetic fuels, reducing the ever-present demand on oil and natural gas to fulfil these needs. The project is within the remit of an international ambition to valorise carbon dioxide waste and reduce environmentally harmful greenhouse gas generation, as opposed to stopping at carbon capture and sequestration. This proposal outlines an alternative route to carbon dioxide utilisation (CDU), in which a mediated approach that decouples the electrochemical reduction from the catalytic process is explored. Novel bimetallic catalysts will be synthesised and studied, meditating electron donating solutions will be generated, and a robust and comprehensive analytical arrangement will be implemented to allow total identification and quantification of the wide range of possible products.
Electrocatalytic CO2 reduction is one of the key approaches to CDU, as it has a direct pathway to carbon neutral renewable electricity. Nonetheless it is a field that has shown minimal progress in the past 30 years. A paradigm shift is necessary in the approach to electrochemical CO2 reduction, where conventional heterogeneous interfacial catalysis is limited by mass transport, passivation, and CO2 solubility. This proposal outlines the use of electron donating mediators generated separately to the catalysed chemical reduction of CO2, such that the electrolyte becomes the electrode. This opens a whole new avenue for catalyst research, and here target bimetallic catalysts that suppress side reactions and promote high value product synthesis are described.
Max ERC Funding
1 499 994 €
Duration
Start date: 2018-10-01, End date: 2023-09-30
Project acronym DEDIGROWTH
Project Dedicated growth of novel 1-dimensional materials for emerging nanotechnological applications
Researcher (PI) Nicole Grobert
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Call Details Starting Grant (StG), PE5, ERC-2009-StG
Summary This proposal aims to establish growth systematics for catalytically grown nanomaterials, such as nanoparticles, nanorods, carbon and hetero-atomic nanotubes. At present there is no clear understanding of the formation mechanism of these structures. Hence, the control over their properties, a vital aspect for technological applications of nanomaterials, is limited and remains difficult. Therefore, the main target of this proposal is the controlled production of new carbon and non-carbon-based nanomaterials with the focus on achieving structural control of the nanomaterials at the atomic level. An essential step towards the controlled generation of such new nanomaterials is a comprehensive understanding of the growth reactions and the role of the metal catalyst involved in the synthesis process. To achieve this, we will use in-situ techniques to study the chemical environment in the reactor during growth and state-of-the-art electron microscopy to reveal the chemical composition of the resulting catalyst particles and structures with atomic resolution. This data will provide information on how the nanostructure may have formed. Theoretical calculations and modelling of atomic scale processes of the catalyst reactivity will be used to draw a consistent picture of the functioning of the catalyst. An improved understanding of the functioning of the catalyst will allow us to estimate how the catalyst particles and reaction conditions have to be modified in order to enhance or to suppress certain products. A new high-throughput synthesis method together with the systematic variation of the growth parameters, such as cluster particle size and composition, temperature, gas pressure and precursor, will be used to generate a nanomaterials growth library. This nanomaterials library will be made available on the Internet for use by other researchers in planning their experiments.
Summary
This proposal aims to establish growth systematics for catalytically grown nanomaterials, such as nanoparticles, nanorods, carbon and hetero-atomic nanotubes. At present there is no clear understanding of the formation mechanism of these structures. Hence, the control over their properties, a vital aspect for technological applications of nanomaterials, is limited and remains difficult. Therefore, the main target of this proposal is the controlled production of new carbon and non-carbon-based nanomaterials with the focus on achieving structural control of the nanomaterials at the atomic level. An essential step towards the controlled generation of such new nanomaterials is a comprehensive understanding of the growth reactions and the role of the metal catalyst involved in the synthesis process. To achieve this, we will use in-situ techniques to study the chemical environment in the reactor during growth and state-of-the-art electron microscopy to reveal the chemical composition of the resulting catalyst particles and structures with atomic resolution. This data will provide information on how the nanostructure may have formed. Theoretical calculations and modelling of atomic scale processes of the catalyst reactivity will be used to draw a consistent picture of the functioning of the catalyst. An improved understanding of the functioning of the catalyst will allow us to estimate how the catalyst particles and reaction conditions have to be modified in order to enhance or to suppress certain products. A new high-throughput synthesis method together with the systematic variation of the growth parameters, such as cluster particle size and composition, temperature, gas pressure and precursor, will be used to generate a nanomaterials growth library. This nanomaterials library will be made available on the Internet for use by other researchers in planning their experiments.
Max ERC Funding
1 276 038 €
Duration
Start date: 2010-02-01, End date: 2016-01-31
Project acronym DenCity
Project Density assemblages: intensity and the city in a global urban age
Researcher (PI) Colin MCFARLANE
Host Institution (HI) UNIVERSITY OF DURHAM
Call Details Consolidator Grant (CoG), SH2, ERC-2017-COG
Summary DenCity offers a new approach for understanding density and its relationship to the city. Density is a defining feature of the city and urban life. Across the world, density is now at the centre of policy and planning agendas to build cities that are environmentally, economically, socially and politically ‘sustainable’. While there is a lively tradition of research on density in the city, we lack an understanding of the different ways in which high densities are lived and perceived by residents. Existing research provides rich resources for how we might define and represent density, how we might arrive at optimum numbers of people in a given area, and how capitalism builds or reduces densities within and between places globally. However, we lack an understanding of how high density – what I call intensity – is understood and experienced by different urban inhabitants, and the implications for how we understand the contemporary city. Developing a ‘density assemblage’ approach, I propose to examine the ways in which residents differently know and relate to intensity, including how it comes to matter, for good or ill. I do so by examining different cases of intensity in the Asian city, from travel and transport hubs, and slums to rooftops. While the 20th century witnessed a general global decrease of urban density in favour of urban sprawl, many Asian cities continue to densify. Asia is the densest and most urbanized part of the planet, and the trend is predicted to continue. I will examine some of the highest densities in the world, including in Hong Kong, Mumbai, Manila, Dhaka, and Tokyo. The different ways in which intensity becomes known and comes to matter for residents will be a vital challenge for understanding life in the urban 21st century, and for how we understand the city.
Summary
DenCity offers a new approach for understanding density and its relationship to the city. Density is a defining feature of the city and urban life. Across the world, density is now at the centre of policy and planning agendas to build cities that are environmentally, economically, socially and politically ‘sustainable’. While there is a lively tradition of research on density in the city, we lack an understanding of the different ways in which high densities are lived and perceived by residents. Existing research provides rich resources for how we might define and represent density, how we might arrive at optimum numbers of people in a given area, and how capitalism builds or reduces densities within and between places globally. However, we lack an understanding of how high density – what I call intensity – is understood and experienced by different urban inhabitants, and the implications for how we understand the contemporary city. Developing a ‘density assemblage’ approach, I propose to examine the ways in which residents differently know and relate to intensity, including how it comes to matter, for good or ill. I do so by examining different cases of intensity in the Asian city, from travel and transport hubs, and slums to rooftops. While the 20th century witnessed a general global decrease of urban density in favour of urban sprawl, many Asian cities continue to densify. Asia is the densest and most urbanized part of the planet, and the trend is predicted to continue. I will examine some of the highest densities in the world, including in Hong Kong, Mumbai, Manila, Dhaka, and Tokyo. The different ways in which intensity becomes known and comes to matter for residents will be a vital challenge for understanding life in the urban 21st century, and for how we understand the city.
Max ERC Funding
1 344 681 €
Duration
Start date: 2018-09-01, End date: 2022-08-31
Project acronym DESI_JEDI-IMAGING
Project Development of mass spectrometric techniques for 3D imaging and in-vivo analysis of biological tissues
Researcher (PI) Zoltan Takats
Host Institution (HI) IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE
Call Details Starting Grant (StG), PE4, ERC-2007-StG
Summary Recent development of atmospheric pressure desorption ionization methods has opened a unique area of application for analytical mass spectrometry. Most of these methods do not require any modification of samples, and this feature, together with the minimal invasiveness of these methods allows direct analytical interrogation of biological tissues, even the real-time, in-vivo observation of biochemical processes. The proposed research focuses on the development of atmospheric pressure desorption ionization mass spectrometric methods for the characterization of biological tissues. The first question to answer is aimed at the nature of information which can be obtained, using a variety of desorption ionization methods including desorption electrospray ionization and jet desorption ionization methods. Preliminary results show, that APDI-MS methods provide information on lipids, metabolic compounds, drugs and certain proteins. First task of the proposed research is to implement a chemical imaging system, which is capable of producing 3D concentration distribution functions for various constituents of tissue samples. The developed methodology will be used to tackle fundamental pathophysiological problems including development of various malignant tumors. A database will be created for the unequivocal identification of various tissues including healthy and malignant tissue samples. In-vivo applications of MS will also be developed. JeDI-MS,similarly to water jet surgery, also utilizes high velocity water jet can directly be used as an intelligent scalpel. Real-time in-situ tissue identification has the potential of revolutionizing cancer surgery, since this way the amount of removed tissue can be minimized, while the tumor removal efficiency is maximized. The identical experimental platform can also be used to gather real-time in-situ metabolic information, which can help to understand pathophysiological changes.
Summary
Recent development of atmospheric pressure desorption ionization methods has opened a unique area of application for analytical mass spectrometry. Most of these methods do not require any modification of samples, and this feature, together with the minimal invasiveness of these methods allows direct analytical interrogation of biological tissues, even the real-time, in-vivo observation of biochemical processes. The proposed research focuses on the development of atmospheric pressure desorption ionization mass spectrometric methods for the characterization of biological tissues. The first question to answer is aimed at the nature of information which can be obtained, using a variety of desorption ionization methods including desorption electrospray ionization and jet desorption ionization methods. Preliminary results show, that APDI-MS methods provide information on lipids, metabolic compounds, drugs and certain proteins. First task of the proposed research is to implement a chemical imaging system, which is capable of producing 3D concentration distribution functions for various constituents of tissue samples. The developed methodology will be used to tackle fundamental pathophysiological problems including development of various malignant tumors. A database will be created for the unequivocal identification of various tissues including healthy and malignant tissue samples. In-vivo applications of MS will also be developed. JeDI-MS,similarly to water jet surgery, also utilizes high velocity water jet can directly be used as an intelligent scalpel. Real-time in-situ tissue identification has the potential of revolutionizing cancer surgery, since this way the amount of removed tissue can be minimized, while the tumor removal efficiency is maximized. The identical experimental platform can also be used to gather real-time in-situ metabolic information, which can help to understand pathophysiological changes.
Max ERC Funding
1 750 000 €
Duration
Start date: 2008-09-01, End date: 2013-08-31
Project acronym DESTABLE
Project Destabilisation of sociotechnical regimes as the key to transitions towards sustainability
Researcher (PI) Frank Geels
Host Institution (HI) THE UNIVERSITY OF SUSSEX
Call Details Starting Grant (StG), SH2, ERC-2007-StG
Summary Sociotechnical transitions are important to address environmental problems. The present literature focuses on green options that break through and replace existing sociotechnical regimes. The project turns the analytical focus upside down, seeing the destabilisation and decline of existing regimes as the key to transitions. Regimes refer to the rules (knowledge base, belief system, mission, strategic orientation) shared by incumbent actors in an industry. Destabilisation results from increasing external pressures (economic, normative, regulatory) and eroding commitment of actors to regime rules. Research questions are: 1 To what degree have regimes in transport, energy and agriculture destabilised in the last 30 years, as a result of environmental pressures? 2 What kind of process is regime destabilisation and how should it be conceptualised for environmental problems? Which mechanisms are important and how do they interact? The project develops a theoretical perspective, combining insights from neo-institutional theory, STS, evolutionary economics. A phase-based pattern and three propositions are advanced. To investigate destabilisation, the project uses case studies as research strategy, which is appropriate for tracing complex processes such as changing beliefs and identities, fuzzy network boundaries, and many interacting (external) factors. Two PhD projects do four longitudinal case studies about destabilisation. Cases are selected with regard to the phase-based pattern and propositions. One case (decline of domestic coal) went though all phases. Another case (destabilisation of pig farming) has progressed far into the last phase. Coal in electricity and the car regime are less far in the phase-pattern, and probably less destabilised. The PI integrates findings from PhD projects, providing general answers to research questions. He also elaborates the inter-disciplinary perspective, and addresses the possibilities for sustainability transitions.
Summary
Sociotechnical transitions are important to address environmental problems. The present literature focuses on green options that break through and replace existing sociotechnical regimes. The project turns the analytical focus upside down, seeing the destabilisation and decline of existing regimes as the key to transitions. Regimes refer to the rules (knowledge base, belief system, mission, strategic orientation) shared by incumbent actors in an industry. Destabilisation results from increasing external pressures (economic, normative, regulatory) and eroding commitment of actors to regime rules. Research questions are: 1 To what degree have regimes in transport, energy and agriculture destabilised in the last 30 years, as a result of environmental pressures? 2 What kind of process is regime destabilisation and how should it be conceptualised for environmental problems? Which mechanisms are important and how do they interact? The project develops a theoretical perspective, combining insights from neo-institutional theory, STS, evolutionary economics. A phase-based pattern and three propositions are advanced. To investigate destabilisation, the project uses case studies as research strategy, which is appropriate for tracing complex processes such as changing beliefs and identities, fuzzy network boundaries, and many interacting (external) factors. Two PhD projects do four longitudinal case studies about destabilisation. Cases are selected with regard to the phase-based pattern and propositions. One case (decline of domestic coal) went though all phases. Another case (destabilisation of pig farming) has progressed far into the last phase. Coal in electricity and the car regime are less far in the phase-pattern, and probably less destabilised. The PI integrates findings from PhD projects, providing general answers to research questions. He also elaborates the inter-disciplinary perspective, and addresses the possibilities for sustainability transitions.
Max ERC Funding
907 114 €
Duration
Start date: 2008-09-01, End date: 2012-11-30
Project acronym DIASPORACONTEST
Project Diasporas and Contested Sovereignty: Transnational Diaspora Mobilization in Europe and Its Impact on Political Proceses in the Balkans, the Caucasus, and the Middle East
Researcher (PI) Maria Velinova Koinova
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary This groundbreaking multi-methods political science study investigates the transnational mobilization of conflict-generated diasporas in Europe and its impact on polities experiencing contested sovereignty in the Balkans, the Caucasus, and the Middle East. Four researchers study how diasporas mobilize when a specific aspect of sovereignty is contested in the original homeland: The PI focuses on the emergence of new states (Kosovo, Nagorno-Karabakh, Palestine). The Post-doc focuses on a secessionist movement (Kurdish separatism in Turkey and Iraqi Kurdistan). The two Ph.D. students focus on challenges to sovereignty stemming from international military intervention (Iraq) and long-term international governance of a weak state (Bosnia-Herzegovina). Since the scholarly field of diasporas and conflicts still lacks theoretical rigor, this study brings a much needed systematization and innovates in several ways. First, it uses a sequential qualitative and quantitative analysis and multi-sited research techniques that have not been utilized so far. Second, the team seeks to develop a typological theory to incorporate in a single framework: 1) diasporic identities, 2) conditions providing political opportunity structures for transnational mobilization, 3) causal mechanisms concatenating in mobilization processes, and 4) transnational diaspora networks, penetrating various local and global institutions. The study further focuses on five levels of analysis: 1) the attitudes of individuals, 2) characteristics of specific groups, 3) five nation-states with different migrant incorporation regimes (France, Germany, the Netherlands, Sweden, and the UK), 4) supranational EU and global institutions penetrated by diaspora networks, 5) and patterns of mobilization specific to a certain region. The project also conducts a cross-country representative survey across 25 country-groups, creating a much needed quantitative dataset, sensitive both to transnationalism and specific context.
Summary
This groundbreaking multi-methods political science study investigates the transnational mobilization of conflict-generated diasporas in Europe and its impact on polities experiencing contested sovereignty in the Balkans, the Caucasus, and the Middle East. Four researchers study how diasporas mobilize when a specific aspect of sovereignty is contested in the original homeland: The PI focuses on the emergence of new states (Kosovo, Nagorno-Karabakh, Palestine). The Post-doc focuses on a secessionist movement (Kurdish separatism in Turkey and Iraqi Kurdistan). The two Ph.D. students focus on challenges to sovereignty stemming from international military intervention (Iraq) and long-term international governance of a weak state (Bosnia-Herzegovina). Since the scholarly field of diasporas and conflicts still lacks theoretical rigor, this study brings a much needed systematization and innovates in several ways. First, it uses a sequential qualitative and quantitative analysis and multi-sited research techniques that have not been utilized so far. Second, the team seeks to develop a typological theory to incorporate in a single framework: 1) diasporic identities, 2) conditions providing political opportunity structures for transnational mobilization, 3) causal mechanisms concatenating in mobilization processes, and 4) transnational diaspora networks, penetrating various local and global institutions. The study further focuses on five levels of analysis: 1) the attitudes of individuals, 2) characteristics of specific groups, 3) five nation-states with different migrant incorporation regimes (France, Germany, the Netherlands, Sweden, and the UK), 4) supranational EU and global institutions penetrated by diaspora networks, 5) and patterns of mobilization specific to a certain region. The project also conducts a cross-country representative survey across 25 country-groups, creating a much needed quantitative dataset, sensitive both to transnationalism and specific context.
Max ERC Funding
1 498 771 €
Duration
Start date: 2012-02-01, End date: 2017-09-30
Project acronym DiCED
Project Digital Campaigning and Electoral Democracy
Researcher (PI) Rachel GIBSON
Host Institution (HI) THE UNIVERSITY OF MANCHESTER
Call Details Advanced Grant (AdG), SH2, ERC-2018-ADG
Summary Overview: This project will set a new agenda and direction for the study of political campaigns. It will examine whether and how new digital technologies are transforming election campaigns and citizen behaviour in new and established democracies. More specifically, it will assess claims that democracies are now entering a new data-driven era of political campaigning that is profoundly reconfiguring how campaigns’ are run, who runs them and their implications for the quality of voter decision-making, the vibrancy of political parties and ultimately, the future of representative democracy. It will do so in three main stages: (1) First, it will define what data-driven campaigning is and critically assess whether it forms new and distinct era of electioneering in conceptual and historical terms? In particular, it will argue that the two key traits of this new mode of campaigning are the increased individualization or micro-targeting of party messages and the automated use of misinformation to mobilize and persuade voters. (2) Based on this definition it will map the ‘supply’ of the new mode of campaigning across new and older democracies by designing an innovative new index to compare use of data-driven techniques by parties. Where is it most commonly seen and why are some parties and countries more likely to promote its growth? (3) Finally, it will assess the impact of these new methods on key political actors and assess the consequences for the longer term future of liberal democracy. Does use of these techniques help counter recent declines in voter turnout by identifying under-mobilized groups? Or, do they ensure parties focus on the already engaged, bypassing those that are harder to reach? Can data-driven campaigning improve citizen choices by giving them the information on the issues they primarily care about or does it help to increase disinformation and even manipulation of voter choices?
Summary
Overview: This project will set a new agenda and direction for the study of political campaigns. It will examine whether and how new digital technologies are transforming election campaigns and citizen behaviour in new and established democracies. More specifically, it will assess claims that democracies are now entering a new data-driven era of political campaigning that is profoundly reconfiguring how campaigns’ are run, who runs them and their implications for the quality of voter decision-making, the vibrancy of political parties and ultimately, the future of representative democracy. It will do so in three main stages: (1) First, it will define what data-driven campaigning is and critically assess whether it forms new and distinct era of electioneering in conceptual and historical terms? In particular, it will argue that the two key traits of this new mode of campaigning are the increased individualization or micro-targeting of party messages and the automated use of misinformation to mobilize and persuade voters. (2) Based on this definition it will map the ‘supply’ of the new mode of campaigning across new and older democracies by designing an innovative new index to compare use of data-driven techniques by parties. Where is it most commonly seen and why are some parties and countries more likely to promote its growth? (3) Finally, it will assess the impact of these new methods on key political actors and assess the consequences for the longer term future of liberal democracy. Does use of these techniques help counter recent declines in voter turnout by identifying under-mobilized groups? Or, do they ensure parties focus on the already engaged, bypassing those that are harder to reach? Can data-driven campaigning improve citizen choices by giving them the information on the issues they primarily care about or does it help to increase disinformation and even manipulation of voter choices?
Max ERC Funding
2 499 394 €
Duration
Start date: 2019-11-01, End date: 2024-10-31
Project acronym DIREVOLFUN
Project Directed Evolution of Function within Chemical Systems: Adaptive Capsules and Polymers
Researcher (PI) Jonathan Russell Nitschke
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Starting Grant (StG), PE5, ERC-2010-StG_20091028
Summary A signature trait of living systems is their ability to dynamically adjust to features of their environments, adapting to stay alive, and evolving to take better advantage of the resources in their environments. This proposed research aims to synthesise new chemical systems that are capable of adaptation and evolution, with the achievement of specified functions being used as the benchmarks by which we may be judged to have succeeded in setting the direction for our systems evolution. Two parallel lines of inquiry will be followed. First, we will build upon results that we have recently published in Science[1] to create a series of new molecular capsules that are capable of dynamically adapting to different guest molecules. These capsules will serve as sensors and as enzyme-like catalysts through the use of transition-state-analogue guests. Second, we will prepare new metal-containing conjugated polymers through self-assembly, which will be capable of dynamically exchanging building blocks in solution. These polymers will have potential applications as electrically-conductive materials, with functional properties that may be tuned and optimised by the application of evolutionary pressures.
The success of these studies will thus create novel materials with uses as self-assembled sensors, catalysts, and electrical conductors. We will also shed light upon the question of how chemical systems may be induced to evolve under selective pressure. These studies thus have long-term bearing upon the questions of how living systems evolved from pre-biological mixtures of molecules.
[1] P. Mal, B. Breiner, K. Rissanen, J.R. Nitschke, Science 2009, 324, 1697-1699.
Summary
A signature trait of living systems is their ability to dynamically adjust to features of their environments, adapting to stay alive, and evolving to take better advantage of the resources in their environments. This proposed research aims to synthesise new chemical systems that are capable of adaptation and evolution, with the achievement of specified functions being used as the benchmarks by which we may be judged to have succeeded in setting the direction for our systems evolution. Two parallel lines of inquiry will be followed. First, we will build upon results that we have recently published in Science[1] to create a series of new molecular capsules that are capable of dynamically adapting to different guest molecules. These capsules will serve as sensors and as enzyme-like catalysts through the use of transition-state-analogue guests. Second, we will prepare new metal-containing conjugated polymers through self-assembly, which will be capable of dynamically exchanging building blocks in solution. These polymers will have potential applications as electrically-conductive materials, with functional properties that may be tuned and optimised by the application of evolutionary pressures.
The success of these studies will thus create novel materials with uses as self-assembled sensors, catalysts, and electrical conductors. We will also shed light upon the question of how chemical systems may be induced to evolve under selective pressure. These studies thus have long-term bearing upon the questions of how living systems evolved from pre-biological mixtures of molecules.
[1] P. Mal, B. Breiner, K. Rissanen, J.R. Nitschke, Science 2009, 324, 1697-1699.
Max ERC Funding
1 357 006 €
Duration
Start date: 2011-01-01, End date: 2016-12-31
Project acronym DISCONEX
Project The Discursive Construction of Academic Excellence.
Classifying SSH Researchers Through Text-Processing Practices
Researcher (PI) Johannes Angermüller
Host Institution (HI) THE UNIVERSITY OF WARWICK
Call Details Starting Grant (StG), SH2, ERC-2012-StG_20111124
Summary DISCONEX investigates two types of text-processing practices by means of which academic researchers are classified in different national and disciplinary fields of the social sciences and humanities (SSH). The research project will produce theoretically informed and empirically grounded insights into the social organization of SSH research. Drawing from constructivist social theory and qualitative methods in discourse analysis and pragmatics, the research team investigates the discursive construction of excellence as a practical accomplishment of readers cooperating with texts. In a first step, we collect CVs from confirmed SSH researchers from France, Germany, the UK and the U.S.. Then we carry out reader interviews to investigate how membership is negotiated in specialized knowledge communities of the SSH. In a second step, we investigate non-academic practices of processing large text collections in order to account for how academic producers are ranked by evaluation professionals and calculative technologies. Finally, by comparing representations of excellence produced by academic and non-academic actors, DISCONEX will show how knowledge producers and ranking experts account for the representations of other types of readers respectively. In the light of the complex interpretive problems involved in the reading and writing of academic texts, we will produce reflexive knowledge on how SSH researchers are classified in the light of new modes of academic knowledge production. Given the important role that written texts play in SSH discourse, the exchange between the sociology of science and discourse analysis can help establish a new field: the social sciences and humanities studies (SSHS).
Summary
DISCONEX investigates two types of text-processing practices by means of which academic researchers are classified in different national and disciplinary fields of the social sciences and humanities (SSH). The research project will produce theoretically informed and empirically grounded insights into the social organization of SSH research. Drawing from constructivist social theory and qualitative methods in discourse analysis and pragmatics, the research team investigates the discursive construction of excellence as a practical accomplishment of readers cooperating with texts. In a first step, we collect CVs from confirmed SSH researchers from France, Germany, the UK and the U.S.. Then we carry out reader interviews to investigate how membership is negotiated in specialized knowledge communities of the SSH. In a second step, we investigate non-academic practices of processing large text collections in order to account for how academic producers are ranked by evaluation professionals and calculative technologies. Finally, by comparing representations of excellence produced by academic and non-academic actors, DISCONEX will show how knowledge producers and ranking experts account for the representations of other types of readers respectively. In the light of the complex interpretive problems involved in the reading and writing of academic texts, we will produce reflexive knowledge on how SSH researchers are classified in the light of new modes of academic knowledge production. Given the important role that written texts play in SSH discourse, the exchange between the sociology of science and discourse analysis can help establish a new field: the social sciences and humanities studies (SSHS).
Max ERC Funding
1 498 959 €
Duration
Start date: 2013-03-01, End date: 2018-08-31
Project acronym DISCOVER
Project Design of Mixed Anion Inorganic Semiconductors for Energy Conversion
Researcher (PI) David SCANLON
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), PE5, ERC-2017-STG
Summary Multi-component systems offer the chemical and structural flexibility necessary to meet the needs of next-generation energy conversion. The vast majority of work in the field has focused on mixed-metal compounds. DISCOVER will computationally explore mixed-anion compounds. These are complex systems that provide significant technical challenges for atomistic and electronic structure modelling. Currently, structure-property relationships are poorly developed and there is a distinct lack of understanding of order-disorder transitions. Crucially, no systematic approach has been established for designing new combinations which can be tailored to match the criteria for technological applications.
This project aims to utilize advanced computational techniques to: (i) understand trends in existing mixed anion systems, and (ii) to employ state of the art crystal structure prediction codes to investigate novel ternary and quaternary mixed-anion compositions. The structure-property information emanating from this analysis will allow us to develop design principles for mixed anion semiconductors, which we will use to predict prototype systems for energy conversion. Promising candidates will be experimentally tested through a collaborative network of experts in the field. This ambitious project will push the boundaries of computational materials design, through the use of both classical and electronic structure simulation techniques for bulk, surface and excited states calculations.
The principle outcome will be a novel understanding of how to controllably design mixed anion semiconductors for technological applications, which will drive this material class to the forefront of materials science, while establishing my group at the frontier of computational materials science.
Summary
Multi-component systems offer the chemical and structural flexibility necessary to meet the needs of next-generation energy conversion. The vast majority of work in the field has focused on mixed-metal compounds. DISCOVER will computationally explore mixed-anion compounds. These are complex systems that provide significant technical challenges for atomistic and electronic structure modelling. Currently, structure-property relationships are poorly developed and there is a distinct lack of understanding of order-disorder transitions. Crucially, no systematic approach has been established for designing new combinations which can be tailored to match the criteria for technological applications.
This project aims to utilize advanced computational techniques to: (i) understand trends in existing mixed anion systems, and (ii) to employ state of the art crystal structure prediction codes to investigate novel ternary and quaternary mixed-anion compositions. The structure-property information emanating from this analysis will allow us to develop design principles for mixed anion semiconductors, which we will use to predict prototype systems for energy conversion. Promising candidates will be experimentally tested through a collaborative network of experts in the field. This ambitious project will push the boundaries of computational materials design, through the use of both classical and electronic structure simulation techniques for bulk, surface and excited states calculations.
The principle outcome will be a novel understanding of how to controllably design mixed anion semiconductors for technological applications, which will drive this material class to the forefront of materials science, while establishing my group at the frontier of computational materials science.
Max ERC Funding
1 499 998 €
Duration
Start date: 2018-02-01, End date: 2023-01-31
Project acronym DIVLAB
Project Consumption Work and Societal Divisions of Labour
Researcher (PI) Miriam Anne Glucksmann
Host Institution (HI) UNIVERSITY OF ESSEX
Call Details Advanced Grant (AdG), SH2, ERC-2009-AdG
Summary Contemporary global developments in work and employment are transforming labour and reshaping relations between workers, creating new webs of interconnection across the world. This research programme aims to radically revise the foundational concept of the division of labour , by situating traditional understandings of the technical allocation of tasks within an expanded theoretical framework. Two additional dimensions of differentiation and interdependency of work activities are proposed, namely across socio-economic modes (market, non-market, etc.) and across the economic processes of production, distribution, exchange, and preparation for consumption. The approach will be developed by opening up a new research terrain of consumption work : all work undertaken by consumers necessary for the purchase, use, re-use and disposal of consumption goods. The work of consumers is shaped by its interdependency with that of providers, and vice versa, so providing a key to route to understanding the overall dynamics and variety of changing worlds of work. Three contrasting empirical probes are chosen for the questions each raises about consumption work and its increasing socio-economic importance: domestic broadband installation, food preparation and household recycling of waste. Analysis will centre for each on the varying nature of the interface and interaction between consumption work and systems of provision in five comparator countries (UK, Sweden, France, Taiwan, Korea) selected for their contrasting socio-economies. The research programme is global, comparative and historical, making a significant scientific and policy contribution, by advancing comprehension of key processes of ongoing socio-economic change, and establishing consumption work as a new field of enquiry.
Summary
Contemporary global developments in work and employment are transforming labour and reshaping relations between workers, creating new webs of interconnection across the world. This research programme aims to radically revise the foundational concept of the division of labour , by situating traditional understandings of the technical allocation of tasks within an expanded theoretical framework. Two additional dimensions of differentiation and interdependency of work activities are proposed, namely across socio-economic modes (market, non-market, etc.) and across the economic processes of production, distribution, exchange, and preparation for consumption. The approach will be developed by opening up a new research terrain of consumption work : all work undertaken by consumers necessary for the purchase, use, re-use and disposal of consumption goods. The work of consumers is shaped by its interdependency with that of providers, and vice versa, so providing a key to route to understanding the overall dynamics and variety of changing worlds of work. Three contrasting empirical probes are chosen for the questions each raises about consumption work and its increasing socio-economic importance: domestic broadband installation, food preparation and household recycling of waste. Analysis will centre for each on the varying nature of the interface and interaction between consumption work and systems of provision in five comparator countries (UK, Sweden, France, Taiwan, Korea) selected for their contrasting socio-economies. The research programme is global, comparative and historical, making a significant scientific and policy contribution, by advancing comprehension of key processes of ongoing socio-economic change, and establishing consumption work as a new field of enquiry.
Max ERC Funding
810 437 €
Duration
Start date: 2010-04-01, End date: 2013-12-31
Project acronym DOS
Project Drugging the Undruggable: Discovery of Protein-Protein Interaction Modulators Using Diversity-Oriented Synthesis
Researcher (PI) David Spring
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Starting Grant (StG), PE5, ERC-2011-StG_20101014
Summary This proposal aims to exploit diversity-oriented synthesis in order to lay the scientific and technological foundations for the development of enzyme inhibition by protein-protein interaction (PPI) modulation as a tool for chemical biology and molecular therapeutics. We will deploy diversity-oriented synthesis lead discovery to explore concepts for PPI modulation in important enzyme families. This work will yield new chemical entities with a spectrum of properties directed against candidate macromolecular interactions important in the regulation of enzymes that mediate key biological pathways. The proposed work has the potential to transform current approaches to drug discovery, and to radically extend the repertoire of tools available for chemical biology. It will help to address the problem of identifying small-molecule inhibitors of PPIs, widely accepted to be of major fundamental and practical significance to biomedical science.
Summary
This proposal aims to exploit diversity-oriented synthesis in order to lay the scientific and technological foundations for the development of enzyme inhibition by protein-protein interaction (PPI) modulation as a tool for chemical biology and molecular therapeutics. We will deploy diversity-oriented synthesis lead discovery to explore concepts for PPI modulation in important enzyme families. This work will yield new chemical entities with a spectrum of properties directed against candidate macromolecular interactions important in the regulation of enzymes that mediate key biological pathways. The proposed work has the potential to transform current approaches to drug discovery, and to radically extend the repertoire of tools available for chemical biology. It will help to address the problem of identifying small-molecule inhibitors of PPIs, widely accepted to be of major fundamental and practical significance to biomedical science.
Max ERC Funding
1 499 723 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym DRONETHICS
Project Emergent Ethics of Drone Violence: Toward a Comprehensive Governance Framework
Researcher (PI) Christian ENEMARK
Host Institution (HI) UNIVERSITY OF SOUTHAMPTON
Call Details Consolidator Grant (CoG), SH2, ERC-2017-COG
Summary The increasing use of armed, uninhabited aircraft (drones) is a serious political challenge with implications for security and justice worldwide. Drone technology is attracting high levels of investment, drones controlled remotely are becoming more numerous, and technological momentum toward drones controlled by artificial intelligence (AI) is building. Many human lives are at stake in this, so the violent use of drones continues to raise ethical questions. DRONETHICS will systematically address an urgent need to clarify the morality of ‘drone violence’, defined as violence involving a weapon system that is radically remote from its immediate user. Such remoteness is achieved through extreme physical distancing or the devolution of agency from humans to machines, so drone violence disrupts traditional expectations about war and a warrior’s exposure to risk. In turn, the disruptively innovative premise of this project is that such violence does not necessarily fall within the remit of the Just War framework according to which war is traditionally judged and governed. Moving beyond state-of-the-art Just War thinking, the project opens up an ethical inquiry into drone violence conceptualised as either war, law enforcement, interpersonal violence, or devolved (to AI) violence. An interdisciplinary research team, incorporating international relations, moral philosophy and computer science perspectives, will conduct rigorous analysis of documentary sources and engage closely with officials, drone operators, and roboticists. Through innovative exploration and application of alternative frameworks for governing violence, DRONETHICS will produce: the first integrated conceptual framework for explaining ethical concerns arising from current and potential forms of drone violence; concrete recommendations for policy-makers on how to manage this violence ethically; and a new normative vision for shaping the longer-term trajectory of drone violence for the good of all humanity.
Summary
The increasing use of armed, uninhabited aircraft (drones) is a serious political challenge with implications for security and justice worldwide. Drone technology is attracting high levels of investment, drones controlled remotely are becoming more numerous, and technological momentum toward drones controlled by artificial intelligence (AI) is building. Many human lives are at stake in this, so the violent use of drones continues to raise ethical questions. DRONETHICS will systematically address an urgent need to clarify the morality of ‘drone violence’, defined as violence involving a weapon system that is radically remote from its immediate user. Such remoteness is achieved through extreme physical distancing or the devolution of agency from humans to machines, so drone violence disrupts traditional expectations about war and a warrior’s exposure to risk. In turn, the disruptively innovative premise of this project is that such violence does not necessarily fall within the remit of the Just War framework according to which war is traditionally judged and governed. Moving beyond state-of-the-art Just War thinking, the project opens up an ethical inquiry into drone violence conceptualised as either war, law enforcement, interpersonal violence, or devolved (to AI) violence. An interdisciplinary research team, incorporating international relations, moral philosophy and computer science perspectives, will conduct rigorous analysis of documentary sources and engage closely with officials, drone operators, and roboticists. Through innovative exploration and application of alternative frameworks for governing violence, DRONETHICS will produce: the first integrated conceptual framework for explaining ethical concerns arising from current and potential forms of drone violence; concrete recommendations for policy-makers on how to manage this violence ethically; and a new normative vision for shaping the longer-term trajectory of drone violence for the good of all humanity.
Max ERC Funding
1 359 348 €
Duration
Start date: 2018-07-01, End date: 2022-06-30
Project acronym DUPLEX
Project Programmable Plastics
Researcher (PI) Christopher Alexander Hunter
Host Institution (HI) THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Call Details Advanced Grant (AdG), PE5, ERC-2012-ADG_20120216
Summary The unique properties of nucleic acids have made them the material of choice for complex nanofabrication. High fidelity formation of duplexes via non-covalent interactions between complementary sequences provides a straightforward approach to molecular programming of multicomponent self-assembly processes. The structure of the nucleic acid backbone and bases can be changed without destroying these properties, suggesting that there are all kinds of unexplored polymeric structures that will also show sequence selective duplex formation. This proposal investigates this rich new area at the interface of supramolecular, biological and polymer chemistry. The appeal of nucleic acids is that we can dial up any desired sequence via chemical solid phase synthesis or via biological template synthesis. With recent advances in polymerisation processes, which proceed under mild conditions compatible with non-covalent chemistry, we are now in a position to develop comparable processes for synthetic polymers. This proposal explores a ground-breaking approach to the synthesis of polymeric systems equipped with defined sequences of recognition sites. The aim is to establish protocols for routine solid phase synthesis of one class of oligomer, which can be used to template the synthesis of different classes of oligomer. This template chemistry will provide tools for polymerisation of conventional monomers using templates to determine the sequence of recognition sites and hence incorporate the selective recognition properties of nucleic acids into bulk polymers like polystyrene. The ability to program polymers with recognition information will open the way to new materials of unprecedented complexity and functionality with applications in all areas of nanotechnology where precise control over macromolecular structure and supramolecular organisation will be used to program mechanical, photochemical and electronic properties into sophisticated assemblies that rival biology.
Summary
The unique properties of nucleic acids have made them the material of choice for complex nanofabrication. High fidelity formation of duplexes via non-covalent interactions between complementary sequences provides a straightforward approach to molecular programming of multicomponent self-assembly processes. The structure of the nucleic acid backbone and bases can be changed without destroying these properties, suggesting that there are all kinds of unexplored polymeric structures that will also show sequence selective duplex formation. This proposal investigates this rich new area at the interface of supramolecular, biological and polymer chemistry. The appeal of nucleic acids is that we can dial up any desired sequence via chemical solid phase synthesis or via biological template synthesis. With recent advances in polymerisation processes, which proceed under mild conditions compatible with non-covalent chemistry, we are now in a position to develop comparable processes for synthetic polymers. This proposal explores a ground-breaking approach to the synthesis of polymeric systems equipped with defined sequences of recognition sites. The aim is to establish protocols for routine solid phase synthesis of one class of oligomer, which can be used to template the synthesis of different classes of oligomer. This template chemistry will provide tools for polymerisation of conventional monomers using templates to determine the sequence of recognition sites and hence incorporate the selective recognition properties of nucleic acids into bulk polymers like polystyrene. The ability to program polymers with recognition information will open the way to new materials of unprecedented complexity and functionality with applications in all areas of nanotechnology where precise control over macromolecular structure and supramolecular organisation will be used to program mechanical, photochemical and electronic properties into sophisticated assemblies that rival biology.
Max ERC Funding
2 457 947 €
Duration
Start date: 2013-03-01, End date: 2019-02-28
Project acronym DUST
Project Data Assimilation for Agent-Based Models: Applications to Civil Emergencies
Researcher (PI) Nicolas Sparrow MALLESON
Host Institution (HI) UNIVERSITY OF LEEDS
Call Details Starting Grant (StG), SH2, ERC-2017-STG
Summary Civil emergencies such as flooding, terrorist attacks, fire, etc., can have devastating impacts on people, infrastructure, and economies. Knowing how to best respond to an emergency can be extremely difficult because building a clear picture of the emerging situation is challenging with the limited data and modelling capabilities that are available. Agent-based modelling (ABM) is a field that excels in its ability to simulate human systems and has therefore become a popular tool for simulating disasters and for modelling strategies that are aimed at mitigating developing problems. However, the field suffers from a serious drawback: models are not able to incorporate up-to-date data (e.g. social media, mobile telephone use, public transport records, etc.). Instead they are initialised with historical data and therefore their forecasts diverge rapidly from reality.
To address this major shortcoming, this research will develop dynamic data assimilation methods for use in ABMs. These techniques have already revolutionised weather forecasts and could offer the same advantages for ABMs of social systems. There are serious methodological barriers that must be overcome, but this research has the potential to produce a step change in the ability of models to create accurate short-term forecasts of social systems. The project is largely methodological, and will evidence the efficacy of the new methods by developing a cutting-edge simulation of a city – entitled the Dynamic Urban Simulation Technique (DUST) – that can be dynamically optimised with streaming ‘big’ data. The model will ultimately be used in three areas of important policy impact: (1) as a tool for understanding and managing cities; (2) as a planning tool for exploring and preparing for potential emergency situations; and (3) as a real-time management tool, drawing on current data as they emerge to create the most reliable picture of the current situation.
Summary
Civil emergencies such as flooding, terrorist attacks, fire, etc., can have devastating impacts on people, infrastructure, and economies. Knowing how to best respond to an emergency can be extremely difficult because building a clear picture of the emerging situation is challenging with the limited data and modelling capabilities that are available. Agent-based modelling (ABM) is a field that excels in its ability to simulate human systems and has therefore become a popular tool for simulating disasters and for modelling strategies that are aimed at mitigating developing problems. However, the field suffers from a serious drawback: models are not able to incorporate up-to-date data (e.g. social media, mobile telephone use, public transport records, etc.). Instead they are initialised with historical data and therefore their forecasts diverge rapidly from reality.
To address this major shortcoming, this research will develop dynamic data assimilation methods for use in ABMs. These techniques have already revolutionised weather forecasts and could offer the same advantages for ABMs of social systems. There are serious methodological barriers that must be overcome, but this research has the potential to produce a step change in the ability of models to create accurate short-term forecasts of social systems. The project is largely methodological, and will evidence the efficacy of the new methods by developing a cutting-edge simulation of a city – entitled the Dynamic Urban Simulation Technique (DUST) – that can be dynamically optimised with streaming ‘big’ data. The model will ultimately be used in three areas of important policy impact: (1) as a tool for understanding and managing cities; (2) as a planning tool for exploring and preparing for potential emergency situations; and (3) as a real-time management tool, drawing on current data as they emerge to create the most reliable picture of the current situation.
Max ERC Funding
1 499 840 €
Duration
Start date: 2018-01-01, End date: 2022-12-31
Project acronym DYNAFLUORS
Project Dynamic Activatable Fluorophores
Researcher (PI) Marc VENDRELL ESCOBAR
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Consolidator Grant (CoG), PE5, ERC-2017-COG
Summary In DYNAFLUORS I will develop the first chemical toolbox for imaging in real time the activity of immune cells in tumours.
Although the management of cancer has improved over the years, the cure rates for patients with metastasis and advanced tumours remain low due to lack of appropriate therapies. Recent studies suggest that drugs empowering host immune cells (i.e. immunotherapies) are promising approaches for intractable tumours. However, there are no tools to visualise and understand how host immune cells stop cancer progression in vivo. This important unmet challenge drives the ambitious targets of this proposal.
Over the past 10 years, I have pioneered the development of chemical fluorophores that allow unparalleled analysis of biological systems. In this project, I will implement an innovative approach to unify cutting-edge methodologies in chemistry and biology and develop Dynamic Activatable Fluorophores (DYNAFLUORS) as a chemical toolbox with enhanced imaging capabilities over current technologies.
The cross-disciplinary and ambitious nature of this project will open multiple avenues for broad impact in many areas of chemistry as well as in basic biology, imaging and medicine. DYNAFLUORS will allow us to image, from the molecular level to human tissue, the activity of immune cells in tumours and the response to therapy in real time. This ground-breaking chemical platform will represent a step forward in the forefront of chemical imaging and will create new opportunities in the personalised management of cancer.
In the long term, DYNAFLUORS will become a transformative toolbox for monitoring disease in humans. The integration of functional fluorophores into imaging technologies to perform ‘optical biopsies’ in vivo and to create patient-specific drug-response assays has the potential to revolutionise the diagnosis, stratification and personalised treatment of disease.
Summary
In DYNAFLUORS I will develop the first chemical toolbox for imaging in real time the activity of immune cells in tumours.
Although the management of cancer has improved over the years, the cure rates for patients with metastasis and advanced tumours remain low due to lack of appropriate therapies. Recent studies suggest that drugs empowering host immune cells (i.e. immunotherapies) are promising approaches for intractable tumours. However, there are no tools to visualise and understand how host immune cells stop cancer progression in vivo. This important unmet challenge drives the ambitious targets of this proposal.
Over the past 10 years, I have pioneered the development of chemical fluorophores that allow unparalleled analysis of biological systems. In this project, I will implement an innovative approach to unify cutting-edge methodologies in chemistry and biology and develop Dynamic Activatable Fluorophores (DYNAFLUORS) as a chemical toolbox with enhanced imaging capabilities over current technologies.
The cross-disciplinary and ambitious nature of this project will open multiple avenues for broad impact in many areas of chemistry as well as in basic biology, imaging and medicine. DYNAFLUORS will allow us to image, from the molecular level to human tissue, the activity of immune cells in tumours and the response to therapy in real time. This ground-breaking chemical platform will represent a step forward in the forefront of chemical imaging and will create new opportunities in the personalised management of cancer.
In the long term, DYNAFLUORS will become a transformative toolbox for monitoring disease in humans. The integration of functional fluorophores into imaging technologies to perform ‘optical biopsies’ in vivo and to create patient-specific drug-response assays has the potential to revolutionise the diagnosis, stratification and personalised treatment of disease.
Max ERC Funding
1 986 650 €
Duration
Start date: 2018-06-01, End date: 2023-05-31
Project acronym DYNAMIN
Project Dynamic Control of Mineralisation
Researcher (PI) Fiona Meldrum
Host Institution (HI) UNIVERSITY OF LEEDS
Call Details Advanced Grant (AdG), PE5, ERC-2017-ADG
Summary This project will take inspiration from biomineralisation to achieve exceptional, dynamic control over crystallisation processes.
Understanding the fundamental mechanisms which govern crystallisation promises the ability to inhibit or promote crystallisation as desired, and to tailor the properties of crystalline materials towards a huge range of applications. Biomineralisation provides a perfect precedent for this approach, where organisms achieve control currently unparalleled in synthetic systems. This is achieved because mineralisation occurs within controlled environments in which an organism can interact with the nascent mineral.
Thanks to recent advances in microfabrication techniques and analytical methods we finally have the tools required to bring such control to the laboratory. DYNAMIN will exploit microfluidic and confined systems to study and interact with crystallisation processes with outstanding spatial and temporal resolution. Flowing droplet devices will be coupled to synchrotron techniques to investigate and control nucleation, using soluble additives and nucleating particles to direct the crystallisation pathway. Static chambers will be used to interact with crystallisation processes over longer length and time scales to achieve spatio-temporal control to rival that in biomineralisation, while a unique confined system – titania nanotubes – will enable the study and control of organic-mediated mineralisation, using fresh reagents and proteinases to interact with the process. Finally, a key biogenic strategy will provide the inspiration to develop a simple and potentially general method to trigger and control the transformation of amorphous precursor phases to single crystal products.
This will generate a new framework for studying and controlling crystallisation processes, where these new skills will find applications in sectors ranging from the Chemical Industry, to Healthcare, Advanced Materials, Formulated Products and the Environment.
Summary
This project will take inspiration from biomineralisation to achieve exceptional, dynamic control over crystallisation processes.
Understanding the fundamental mechanisms which govern crystallisation promises the ability to inhibit or promote crystallisation as desired, and to tailor the properties of crystalline materials towards a huge range of applications. Biomineralisation provides a perfect precedent for this approach, where organisms achieve control currently unparalleled in synthetic systems. This is achieved because mineralisation occurs within controlled environments in which an organism can interact with the nascent mineral.
Thanks to recent advances in microfabrication techniques and analytical methods we finally have the tools required to bring such control to the laboratory. DYNAMIN will exploit microfluidic and confined systems to study and interact with crystallisation processes with outstanding spatial and temporal resolution. Flowing droplet devices will be coupled to synchrotron techniques to investigate and control nucleation, using soluble additives and nucleating particles to direct the crystallisation pathway. Static chambers will be used to interact with crystallisation processes over longer length and time scales to achieve spatio-temporal control to rival that in biomineralisation, while a unique confined system – titania nanotubes – will enable the study and control of organic-mediated mineralisation, using fresh reagents and proteinases to interact with the process. Finally, a key biogenic strategy will provide the inspiration to develop a simple and potentially general method to trigger and control the transformation of amorphous precursor phases to single crystal products.
This will generate a new framework for studying and controlling crystallisation processes, where these new skills will find applications in sectors ranging from the Chemical Industry, to Healthcare, Advanced Materials, Formulated Products and the Environment.
Max ERC Funding
2 632 375 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym DYNAPORE
Project Dynamic responsive porous crystals
Researcher (PI) Matthew ROSSEINSKY
Host Institution (HI) THE UNIVERSITY OF LIVERPOOL
Call Details Advanced Grant (AdG), PE5, ERC-2015-AdG
Summary The project addresses the long-term vision of man-made materials with chemical selectivity and functional efficiency produced by dynamic structural flexibility. These materials are not intended as protein mimics; they are however inspired by nature’s use of flexible rather than rigid systems, with their ability to dynamically restructure around guests and thus perform highly specific chemistry. Such materials would transform chemical processes through their precision, for example by reorganising to accelerate each step of a cascade reaction without reagent or product inhibition. The road to this vision is blocked as we do not have the methodology and understanding to control such materials.
The aim is to develop synergic, multidisciplinary experimental and computational capability to harness the dynamics of flexible crystalline porous solids for function, demonstrated in separation and catalysis. This will enable design and synthesis of materials that controllably adopt distinct structures according to their chemical environment to optimise performance. We will create a new workflow that integrates understanding of the structure-composition-dynamics-property relationship into the materials design and discovery process. This workflow builds on proof-of-concept in (i) chemical control of dynamical restructuring in flexible crystalline porous materials and in the use of dynamics to (ii) enhance function and (iii) guide synthesis.
Crystalline flexible porous materials are selected because crystallinity maximises the atomic-scale understanding generated, which is transferable to other materials classes, whilst porosity permits sorption and organisation of guests that controls function.
This inorganic materials chemistry project develops integrated capability in chemical synthesis (new metal-organic frameworks and linkers), computation (prediction and evaluation of structure and dynamical guest response), characterisation (e.g. by diffraction) and measurement of function.
Summary
The project addresses the long-term vision of man-made materials with chemical selectivity and functional efficiency produced by dynamic structural flexibility. These materials are not intended as protein mimics; they are however inspired by nature’s use of flexible rather than rigid systems, with their ability to dynamically restructure around guests and thus perform highly specific chemistry. Such materials would transform chemical processes through their precision, for example by reorganising to accelerate each step of a cascade reaction without reagent or product inhibition. The road to this vision is blocked as we do not have the methodology and understanding to control such materials.
The aim is to develop synergic, multidisciplinary experimental and computational capability to harness the dynamics of flexible crystalline porous solids for function, demonstrated in separation and catalysis. This will enable design and synthesis of materials that controllably adopt distinct structures according to their chemical environment to optimise performance. We will create a new workflow that integrates understanding of the structure-composition-dynamics-property relationship into the materials design and discovery process. This workflow builds on proof-of-concept in (i) chemical control of dynamical restructuring in flexible crystalline porous materials and in the use of dynamics to (ii) enhance function and (iii) guide synthesis.
Crystalline flexible porous materials are selected because crystallinity maximises the atomic-scale understanding generated, which is transferable to other materials classes, whilst porosity permits sorption and organisation of guests that controls function.
This inorganic materials chemistry project develops integrated capability in chemical synthesis (new metal-organic frameworks and linkers), computation (prediction and evaluation of structure and dynamical guest response), characterisation (e.g. by diffraction) and measurement of function.
Max ERC Funding
2 493 425 €
Duration
Start date: 2016-10-01, End date: 2021-09-30
Project acronym EBDD
Project Beyond structure: integrated computational and experimental approach to Ensemble-Based Drug Design
Researcher (PI) Julien Michel
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Call Details Starting Grant (StG), PE4, ERC-2013-StG
Summary "Although protein dynamics plays an essential role in function, it is rarely considered explicitly in current structure-based approaches to drug design. Here I propose the computer-aided design of ligands by modulation of protein dynamics, or equivalently, protein structural ensembles. The detailed understanding of ligand-induced perturbations of protein dynamics that will result from this study is crucial not just to accurately predicting binding affinities and tackling ""undruggable"" targets, but also to understanding protein allostery.
Three major aims will be pursued during this project.
First, I will combine concepts from chemoinformatics and non-equilibrium thermodynamics to detect cryptic ""druggable"" small molecule binding sites in computed structural ensembles. New computational methods will be developed to predict how binding at these putative sites is likely to influence protein function. This will enable rational approaches to allosteric control of protein function.
Second, new classes of non-equilibrium sampling algorithms will be developed to improve by 2-3 orders of magnitude the speed of computation of protein/ligand structural ensembles by molecular simulations. This will enable routine consideration of protein flexibility in ligand optimisation problems.
Third, I will address with the above methods a frontier problem in molecular recognition: the rational design of protein isoform-specific ligands. To achieve this goal, I will integrate computation with experiments and focus efforts on the therapeutically relevant cyclophilin protein family. Experimental work will involve the use of purchased or custom-synthesized competitive and allosteric ligands in enzymatic assays, calorimetry and crystal structure analyses.
Overall, this project proposes fundamental advances in our ability to quantify and engineer protein-ligand interactions, therefore expanding opportunities for the development of future small molecule therapeutics."
Summary
"Although protein dynamics plays an essential role in function, it is rarely considered explicitly in current structure-based approaches to drug design. Here I propose the computer-aided design of ligands by modulation of protein dynamics, or equivalently, protein structural ensembles. The detailed understanding of ligand-induced perturbations of protein dynamics that will result from this study is crucial not just to accurately predicting binding affinities and tackling ""undruggable"" targets, but also to understanding protein allostery.
Three major aims will be pursued during this project.
First, I will combine concepts from chemoinformatics and non-equilibrium thermodynamics to detect cryptic ""druggable"" small molecule binding sites in computed structural ensembles. New computational methods will be developed to predict how binding at these putative sites is likely to influence protein function. This will enable rational approaches to allosteric control of protein function.
Second, new classes of non-equilibrium sampling algorithms will be developed to improve by 2-3 orders of magnitude the speed of computation of protein/ligand structural ensembles by molecular simulations. This will enable routine consideration of protein flexibility in ligand optimisation problems.
Third, I will address with the above methods a frontier problem in molecular recognition: the rational design of protein isoform-specific ligands. To achieve this goal, I will integrate computation with experiments and focus efforts on the therapeutically relevant cyclophilin protein family. Experimental work will involve the use of purchased or custom-synthesized competitive and allosteric ligands in enzymatic assays, calorimetry and crystal structure analyses.
Overall, this project proposes fundamental advances in our ability to quantify and engineer protein-ligand interactions, therefore expanding opportunities for the development of future small molecule therapeutics."
Max ERC Funding
1 382 202 €
Duration
Start date: 2013-12-01, End date: 2018-11-30
Project acronym ECO-ZEN
Project Enabling Catalytic Cross Couplings with only Zinc Electrophiles, Nucleophiles and Boranes
Researcher (PI) Michael James INGLESON
Host Institution (HI) THE UNIVERSITY OF MANCHESTER
Call Details Consolidator Grant (CoG), PE5, ERC-2017-COG
Summary This high-impact, challenging CoG Proposal integrates multiple novel ideas in boron and zinc chemistry into an overarching project to open up new horizons across synthesis and catalysis. The Applicant’s successful ERC StG has opened up new avenues of pioneering research in main group element mediated transformations that were not conceivable before the work was done. Components of this proposal extend out from the StG into new, exciting research areas that are completely different. Developing low toxicity earth abundant catalysts for important transformations is vital to the EU with the focus herein being on; (i) the Suzuki-Miyaura (S-M) cross coupling reaction which is ubiquitous in industry and academia, and (ii) the formation of organoboranes that are essential synthetic intermediates. Both of these are currently dominated by toxic, expensive and low abundance precious metal catalysts (e.g. Pd, Ir). This project will deliver innovation through utilising combinations of main group Lewis acids and nucleophilic anions that do not react with each other, i.e. are frustrated pairs. This “frustration” enables the two species to concertedly transform substrates to achieve:
(i) Precious metal-free S-M cross coupling reactions of sp3C electrophiles catalysed by zinc and boron compounds, including stereospecific couplings and one pot two step cross electrophile couplings.
(ii) Trans-elementoboration of alkynes, including the unprecedented fluoroboration of alkynes.
Other new approaches will be developed to access novel (hetero)arylboronic acid derivatives using only simple boranes and without requiring noble metal catalysts, specifically: (i) boron directed C-H borylation and (ii) directed ortho borylation to enable subsequent meta selective SEAr C-H functionalisation.
This CoG will afford the freedom and impetus via consolidated funding to undertake fundamental research to deliver high impact results, including developing a new area of cross coupling catalysis research.
Summary
This high-impact, challenging CoG Proposal integrates multiple novel ideas in boron and zinc chemistry into an overarching project to open up new horizons across synthesis and catalysis. The Applicant’s successful ERC StG has opened up new avenues of pioneering research in main group element mediated transformations that were not conceivable before the work was done. Components of this proposal extend out from the StG into new, exciting research areas that are completely different. Developing low toxicity earth abundant catalysts for important transformations is vital to the EU with the focus herein being on; (i) the Suzuki-Miyaura (S-M) cross coupling reaction which is ubiquitous in industry and academia, and (ii) the formation of organoboranes that are essential synthetic intermediates. Both of these are currently dominated by toxic, expensive and low abundance precious metal catalysts (e.g. Pd, Ir). This project will deliver innovation through utilising combinations of main group Lewis acids and nucleophilic anions that do not react with each other, i.e. are frustrated pairs. This “frustration” enables the two species to concertedly transform substrates to achieve:
(i) Precious metal-free S-M cross coupling reactions of sp3C electrophiles catalysed by zinc and boron compounds, including stereospecific couplings and one pot two step cross electrophile couplings.
(ii) Trans-elementoboration of alkynes, including the unprecedented fluoroboration of alkynes.
Other new approaches will be developed to access novel (hetero)arylboronic acid derivatives using only simple boranes and without requiring noble metal catalysts, specifically: (i) boron directed C-H borylation and (ii) directed ortho borylation to enable subsequent meta selective SEAr C-H functionalisation.
This CoG will afford the freedom and impetus via consolidated funding to undertake fundamental research to deliver high impact results, including developing a new area of cross coupling catalysis research.
Max ERC Funding
2 070 093 €
Duration
Start date: 2018-05-01, End date: 2023-04-30
Project acronym ECONPUBLIC
Project "Economics in the Public Sphere: USA, UK, France, Brazil and Argentina since 1945"
Researcher (PI) Tiago Jorge Fernandes Da Mata
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Starting Grant (StG), SH2, ERC-2011-StG_20101124
Summary "Media reporting on the economy is never far from controversy. Academic economists and the public regularly find journalists at fault in their interpretation of events and prescription of solutions. Past scholarship has sought to locate the biases of journalists in political and institutional contexts. This project takes a novel approach by studying “economic journalism” as a site for the production of public economic knowledge. The practices of journalists are examined to reveal how they parse competing claims of expertise by academic economists, other social scientists and by laymen. The second half of the twentieth century was witness to increased homogeneity in academic economics and interdependence of national economies, yet the content and style of “economic journalism” has remained distinctive across nations. This project sets out to understand how and why media representation of economic knowledge has remained distinctively different even while the content and style of economics converged internationally. The project aims to understand this differentiation by focusing on three international economic controversies: the reconstruction debate post 1945, the monetary and oil crisis of the 1970s, and the current economic crisis; across five nations: USA, UK, France, Argentina, and Brazil. It combines archival research, oral history, ethnographic observation, content and textual analysis of media, to identify media representations of economic expertise and reveal how they are shaped by historical and cultural contexts. Cultural standards of trust, the history and economics of the media, and the history of economics and social movements explain the emergence of distinct national genres of “economic journalism.” The project offers a original perspective on how public knowledge of the economy is a iterative process engaging journalists, academics and laymen and explores its implications for the possibilities of public support for economic actions and policies."
Summary
"Media reporting on the economy is never far from controversy. Academic economists and the public regularly find journalists at fault in their interpretation of events and prescription of solutions. Past scholarship has sought to locate the biases of journalists in political and institutional contexts. This project takes a novel approach by studying “economic journalism” as a site for the production of public economic knowledge. The practices of journalists are examined to reveal how they parse competing claims of expertise by academic economists, other social scientists and by laymen. The second half of the twentieth century was witness to increased homogeneity in academic economics and interdependence of national economies, yet the content and style of “economic journalism” has remained distinctive across nations. This project sets out to understand how and why media representation of economic knowledge has remained distinctively different even while the content and style of economics converged internationally. The project aims to understand this differentiation by focusing on three international economic controversies: the reconstruction debate post 1945, the monetary and oil crisis of the 1970s, and the current economic crisis; across five nations: USA, UK, France, Argentina, and Brazil. It combines archival research, oral history, ethnographic observation, content and textual analysis of media, to identify media representations of economic expertise and reveal how they are shaped by historical and cultural contexts. Cultural standards of trust, the history and economics of the media, and the history of economics and social movements explain the emergence of distinct national genres of “economic journalism.” The project offers a original perspective on how public knowledge of the economy is a iterative process engaging journalists, academics and laymen and explores its implications for the possibilities of public support for economic actions and policies."
Max ERC Funding
1 458 041 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym ELHO
Project The Age of Hostility: Understanding the Nature, Dynamics, Determinants, and Consequences of Citizens' Electoral Hostility in 27 Democracies
Researcher (PI) Michael BRUTER
Host Institution (HI) LONDON SCHOOL OF ECONOMICS AND POLITICAL SCIENCE
Call Details Advanced Grant (AdG), SH2, ERC-2017-ADG
Summary ‘I hate Brexiteers, they betrayed my future’. Those words of an 18 year old on Brexit Referendum Night represent a growing and worrying phenomenon: electoral hostility. Electoral disagreements have long been seen as results of social divisions, but recent research shows that they have become a basis of antagonism in their own right in the US. Two comparative pilots I ran also found electoral hostility widespread in recent French and British elections but rare in South Africa and Australia. In the UK Brexit referendum, 51% of citizens felt anger towards opposite voters and 46% disgust.
I define electoral hostility as negative feelings (frustration, anger, contempt, disgust) held towards individuals or groups as a result of their effective or perceived electoral preferences. It may occur in the campaign, post-election, and reinforce into self-perpetuating cycles of hostility as it is structured as a Mokken scale which can become ‘stages’ of hostility. While scepticism of political elites is well-studied, hostility towards fellow voters takes electoral negativity to a new level. Electoral hostility may have far reaching consequences, leading citizens to resent one another due to electoral stances and drift apart in increasingly divided societies, but also to the delegitimization of electoral outcomes and negative attitudes towards solidarity.
ELHO will answer the following research question: What are the causes and consequences of electoral hostility at individual, group, and aggregate levels and how does it develop over time? The project’s innovative methods combine a 27 country multi-level panel survey, visual, physiological and field experiments, election diaries, family focus groups, a scoping survey of Election Management Bodies, and campaign and atmosphere coding. The project will also explore possible mitigation in ambitious partnership with psychiatrists, ergonomists, lawyers, EMBs and IGOs creating new Electoral Hostility Research Centre and Observatory.
Summary
‘I hate Brexiteers, they betrayed my future’. Those words of an 18 year old on Brexit Referendum Night represent a growing and worrying phenomenon: electoral hostility. Electoral disagreements have long been seen as results of social divisions, but recent research shows that they have become a basis of antagonism in their own right in the US. Two comparative pilots I ran also found electoral hostility widespread in recent French and British elections but rare in South Africa and Australia. In the UK Brexit referendum, 51% of citizens felt anger towards opposite voters and 46% disgust.
I define electoral hostility as negative feelings (frustration, anger, contempt, disgust) held towards individuals or groups as a result of their effective or perceived electoral preferences. It may occur in the campaign, post-election, and reinforce into self-perpetuating cycles of hostility as it is structured as a Mokken scale which can become ‘stages’ of hostility. While scepticism of political elites is well-studied, hostility towards fellow voters takes electoral negativity to a new level. Electoral hostility may have far reaching consequences, leading citizens to resent one another due to electoral stances and drift apart in increasingly divided societies, but also to the delegitimization of electoral outcomes and negative attitudes towards solidarity.
ELHO will answer the following research question: What are the causes and consequences of electoral hostility at individual, group, and aggregate levels and how does it develop over time? The project’s innovative methods combine a 27 country multi-level panel survey, visual, physiological and field experiments, election diaries, family focus groups, a scoping survey of Election Management Bodies, and campaign and atmosphere coding. The project will also explore possible mitigation in ambitious partnership with psychiatrists, ergonomists, lawyers, EMBs and IGOs creating new Electoral Hostility Research Centre and Observatory.
Max ERC Funding
2 499 838 €
Duration
Start date: 2019-04-01, End date: 2024-03-31
Project acronym EMERGE
Project Enzyme Driven Molecular Nanosystems
Researcher (PI) Rein V Ulijn
Host Institution (HI) UNIVERSITY OF STRATHCLYDE
Call Details Starting Grant (StG), PE5, ERC-2010-StG_20091028
Summary Functional nanomaterials are predicted to have an enormous impact on some of the most pressing issues of 21st century society, including next-generation health care and energy related technologies. Bottom-up approaches, using self-assembly principles, are increasingly considered to be the most appropriate routes for their synthesis. Indeed, Science magazine highlighted How far can we push chemical self-assembly? as one of the 25 biggest questions that face scientific inquiry over the next quarter century. Despite significant advances in recent years, it is still a major challenge to access precisely defined nano-structures in the laboratory, especially if these do not represent the global free energy minimum (i.e. are asymmetric, multifunctional, compartmentalized and/or dynamic). The biological world provides numerous outstanding examples of highly complex functional nano-scale architectures with attractive features such as defect repair, adaptability, molecular recognition and programmability. It is the objective of this ERC Starting Grant to develop and exploit the concept of (bio-)catalytic self-assembly, a bio-inspired approach for bottom-up synthesis of complex nanomaterials. We will explore three unique features of these systems (i) spatiotemporal control, (ii) catalytic amplification, either towards or away from equilibrium and the tempting vision of (iii) dynamic systems with emergent properties. In our approach we aim to encompass the entire spectrum from fundamental understanding to eventual societal benefit. Alongside the fundamental aims, we wish to put our methodologies to use, in collaboration with experts in these fields, to develop novel functional materials towards applications in next-generation biomaterials and gel-phase supramolecular (opto-) electronic materials.
Summary
Functional nanomaterials are predicted to have an enormous impact on some of the most pressing issues of 21st century society, including next-generation health care and energy related technologies. Bottom-up approaches, using self-assembly principles, are increasingly considered to be the most appropriate routes for their synthesis. Indeed, Science magazine highlighted How far can we push chemical self-assembly? as one of the 25 biggest questions that face scientific inquiry over the next quarter century. Despite significant advances in recent years, it is still a major challenge to access precisely defined nano-structures in the laboratory, especially if these do not represent the global free energy minimum (i.e. are asymmetric, multifunctional, compartmentalized and/or dynamic). The biological world provides numerous outstanding examples of highly complex functional nano-scale architectures with attractive features such as defect repair, adaptability, molecular recognition and programmability. It is the objective of this ERC Starting Grant to develop and exploit the concept of (bio-)catalytic self-assembly, a bio-inspired approach for bottom-up synthesis of complex nanomaterials. We will explore three unique features of these systems (i) spatiotemporal control, (ii) catalytic amplification, either towards or away from equilibrium and the tempting vision of (iii) dynamic systems with emergent properties. In our approach we aim to encompass the entire spectrum from fundamental understanding to eventual societal benefit. Alongside the fundamental aims, we wish to put our methodologies to use, in collaboration with experts in these fields, to develop novel functional materials towards applications in next-generation biomaterials and gel-phase supramolecular (opto-) electronic materials.
Max ERC Funding
1 500 000 €
Duration
Start date: 2011-01-01, End date: 2015-12-31
Project acronym EMERGING SUBJECTS
Project Emerging Subjects of the New Economy: Tracing Economic Growth in Mongolia
Researcher (PI) Rebecca Anna Empson Mannerfelt
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Call Details Consolidator Grant (CoG), SH2, ERC-2013-CoG
Summary This project examines how predicted economic growth is experienced by people in Mongolia with the advent of large-scale mining operations. Our project will generate new insight into two areas of concern for economic anthropology and beyond. First we will examine the way that the economy is unfolding in a distinct way in East Asia through different kinds of predictive narratives that come to have an effect on the way people act. Second we will explore how individual subjects also shape the economy in their everyday relations through various forms of exchange and the accumulation of wealth.
This dual focus provides the basis for a nuanced and powerful critique of our understanding of the way in which economic realities are shaped through predictive narratives as well as formed, from the ground-up, by local actors who carve out new forms of subjectivity through such actions. Indeed it is our suggestion that these new subjects of the growing economy are distinctly different from the post-socialist selves described in previous literature on the region. Instead they are powerful and hopeful subjects who demand a different kind of engagement and entitlement. The form such engagement takes and the kind of economic realities produced out of such forms is the focus of our study.
Summary
This project examines how predicted economic growth is experienced by people in Mongolia with the advent of large-scale mining operations. Our project will generate new insight into two areas of concern for economic anthropology and beyond. First we will examine the way that the economy is unfolding in a distinct way in East Asia through different kinds of predictive narratives that come to have an effect on the way people act. Second we will explore how individual subjects also shape the economy in their everyday relations through various forms of exchange and the accumulation of wealth.
This dual focus provides the basis for a nuanced and powerful critique of our understanding of the way in which economic realities are shaped through predictive narratives as well as formed, from the ground-up, by local actors who carve out new forms of subjectivity through such actions. Indeed it is our suggestion that these new subjects of the growing economy are distinctly different from the post-socialist selves described in previous literature on the region. Instead they are powerful and hopeful subjects who demand a different kind of engagement and entitlement. The form such engagement takes and the kind of economic realities produced out of such forms is the focus of our study.
Max ERC Funding
1 658 373 €
Duration
Start date: 2014-09-01, End date: 2019-06-30