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
Country United Kingdom
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 HONORLOGIC
Project The Cultural Logic of Honor and Social Interaction: A Cross-Cultural Comparison
Researcher (PI) Ayse USKUL
Host Institution (HI) UNIVERSITY OF KENT
Country United Kingdom
Call Details Consolidator Grant (CoG), SH3, ERC-2018-COG
Summary Understanding (un)willingness to coordinate with others, to compromise when faced with different choices, or to apologize for transgressions is crucial as these behaviors can act as strong facilitators or inhibitors of important interpersonal processes such as negotiations and coalition building. These behaviors play a major role when individuals from different cultural backgrounds work together to solve disputes or address joint challenges. Yet, we know little about what these behaviors mean in different cultural groups or how they are approached. With HONORLOGIC, I aim to initiate a step-change in our understanding of cultural variation in these important domains of social behavior by providing unique, multimethod, comparative and converging evidence from a wide range of cultural groups. I will answer the question “How do cultural groups that promote honor as a core cultural value approach coordinating with others, reaching compromise, and offering apologies?” by integrating insights from social/cultural psychology, behavioral economics, and anthropology. I will do this by collecting quantitative data using economic games, experiments, and surveys from Spain, Italy, Greece, Turkey, Cyprus, Lebanon, Egypt and Tunisia, as cultural groups where honor has been shown to play a defining role in individuals’ social worlds. I will also run the proposed studies in the US, the UK, Japan and Korea to provide a broader comparative perspective.
HONORLOGIC will produce transformative evidence for theories of social interaction and decision making in psychology, economics, and evolutionary science by (a) producing innovative theory and data with an interdisciplinary and multi-method approach, (b) increasing the diversity of the existing evidence pool, (c) testing established theoretical assumptions in new cultural groups, and (d) contributing to capacity building in under-researched cultural groups in psychological research.
Summary
Understanding (un)willingness to coordinate with others, to compromise when faced with different choices, or to apologize for transgressions is crucial as these behaviors can act as strong facilitators or inhibitors of important interpersonal processes such as negotiations and coalition building. These behaviors play a major role when individuals from different cultural backgrounds work together to solve disputes or address joint challenges. Yet, we know little about what these behaviors mean in different cultural groups or how they are approached. With HONORLOGIC, I aim to initiate a step-change in our understanding of cultural variation in these important domains of social behavior by providing unique, multimethod, comparative and converging evidence from a wide range of cultural groups. I will answer the question “How do cultural groups that promote honor as a core cultural value approach coordinating with others, reaching compromise, and offering apologies?” by integrating insights from social/cultural psychology, behavioral economics, and anthropology. I will do this by collecting quantitative data using economic games, experiments, and surveys from Spain, Italy, Greece, Turkey, Cyprus, Lebanon, Egypt and Tunisia, as cultural groups where honor has been shown to play a defining role in individuals’ social worlds. I will also run the proposed studies in the US, the UK, Japan and Korea to provide a broader comparative perspective.
HONORLOGIC will produce transformative evidence for theories of social interaction and decision making in psychology, economics, and evolutionary science by (a) producing innovative theory and data with an interdisciplinary and multi-method approach, (b) increasing the diversity of the existing evidence pool, (c) testing established theoretical assumptions in new cultural groups, and (d) contributing to capacity building in under-researched cultural groups in psychological research.
Max ERC Funding
1 998 694 €
Duration
Start date: 2019-09-01, End date: 2024-08-31
Project acronym Liquid2DM
Project Two-dimensional liquid cell dielectric microscopy
Researcher (PI) Laura FUMAGALLI
Host Institution (HI) THE UNIVERSITY OF MANCHESTER
Country United Kingdom
Call Details Consolidator Grant (CoG), PE4, ERC-2018-COG
Summary Understanding molecular organization and dynamics which are governed by electrostatic and electrodynamics interactions on the nanoscale requires the measurement of dielectric polarization at the molecular level. Yet, this has remained a formidable challenge because standard dielectric spectroscopy is limited to the micrometer scale that is achieved by using microfabricated electrodes at low frequencies and optical approaches at high frequencies. At the same time, despite the advances in atomistic calculations, theorists struggle to predict dielectric polarization when the system approaches molecular sizes. During the last years I pioneered the development of scanning dielectric microscopy, measuring the dielectric constants of nano-objects as small as tens of nanometers in size - a resolution unparalleled world-wide. In the next five years, I will push the boundaries of the technique and probe the polarizability of liquids and biological macromolecules under two-dimensional (2D) confinement by implementing novel experimental and theoretical approaches. By engineering 2D liquid cells with controlled properties by van der Waals assembly, I will probe polarization and thermodynamic properties of nanoconfined molecular liquids for the first time on the molecular scale with fundamental implications for physical and life sciences. It will provide the experimental data to validate first-principles predictions and mean-field computational methods on which the study of condensed/soft matter and molecular biology is based. The proposal will exploit my current lead to access a key physical property of matter that has remained unknown so far, enabling a wealth of new science in a vast range of research fields, from physical sciences to chemistry and biology, and facilitating the design of devices with novel functionalities.
Summary
Understanding molecular organization and dynamics which are governed by electrostatic and electrodynamics interactions on the nanoscale requires the measurement of dielectric polarization at the molecular level. Yet, this has remained a formidable challenge because standard dielectric spectroscopy is limited to the micrometer scale that is achieved by using microfabricated electrodes at low frequencies and optical approaches at high frequencies. At the same time, despite the advances in atomistic calculations, theorists struggle to predict dielectric polarization when the system approaches molecular sizes. During the last years I pioneered the development of scanning dielectric microscopy, measuring the dielectric constants of nano-objects as small as tens of nanometers in size - a resolution unparalleled world-wide. In the next five years, I will push the boundaries of the technique and probe the polarizability of liquids and biological macromolecules under two-dimensional (2D) confinement by implementing novel experimental and theoretical approaches. By engineering 2D liquid cells with controlled properties by van der Waals assembly, I will probe polarization and thermodynamic properties of nanoconfined molecular liquids for the first time on the molecular scale with fundamental implications for physical and life sciences. It will provide the experimental data to validate first-principles predictions and mean-field computational methods on which the study of condensed/soft matter and molecular biology is based. The proposal will exploit my current lead to access a key physical property of matter that has remained unknown so far, enabling a wealth of new science in a vast range of research fields, from physical sciences to chemistry and biology, and facilitating the design of devices with novel functionalities.
Max ERC Funding
1 998 829 €
Duration
Start date: 2019-10-01, End date: 2024-09-30
Project acronym PHOTOMASS
Project Imaging Biomolecular Self-Assembly with a Molecular Photonic Scale
Researcher (PI) Philipp KUKURA
Host Institution (HI) THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Country United Kingdom
Call Details Consolidator Grant (CoG), PE4, ERC-2018-COG
Summary We propose to transform our understanding of biomolecular interactions and self-assembly by directly visualising the associated molecular mechanisms. To achieve this, we will capitalise on our recent development of interferometric scattering mass spectrometry (iSCAMS), which enables not only the detection and imaging of single biomolecules in solution, but also the accurate determination of their molecular mass at the single molecule level. These studies, and the development of the associated technology, will bridge the gap between high-resolution structural and low-resolution solution-based methods for studies of biomolecular interactions and assembly. We will achieve these ambitious goals by pursuing five interconnected objectives chosen according to their potential to maximise scientific and societal impact by addressing fundamental questions related to biological function and health: (1) Determine the physicochemical origins of mono- and polydispersity; (2) Visualise the mechanism of viral capsid assembly; (3) Reveal the molecular basis of cytoskeletal dynamics; (4) Capture the aggregation and inhibition of amyloid aggregation. These four system-oriented objectives will be accompanied by a technological objective, (5) aimed at implementing improvements in terms of dynamic range and resolution of iSCAMS required for studying self-assembly. As a consequence of the universal applicability of our approach for characterising molecular interactions, oligomeric distributions and dynamics in a facile fashion in solution, this ambitious project opens up a broad range of exciting applications beyond molecular biophysics in fields as drug-discovery, bioanalytical and biomedical science.
Summary
We propose to transform our understanding of biomolecular interactions and self-assembly by directly visualising the associated molecular mechanisms. To achieve this, we will capitalise on our recent development of interferometric scattering mass spectrometry (iSCAMS), which enables not only the detection and imaging of single biomolecules in solution, but also the accurate determination of their molecular mass at the single molecule level. These studies, and the development of the associated technology, will bridge the gap between high-resolution structural and low-resolution solution-based methods for studies of biomolecular interactions and assembly. We will achieve these ambitious goals by pursuing five interconnected objectives chosen according to their potential to maximise scientific and societal impact by addressing fundamental questions related to biological function and health: (1) Determine the physicochemical origins of mono- and polydispersity; (2) Visualise the mechanism of viral capsid assembly; (3) Reveal the molecular basis of cytoskeletal dynamics; (4) Capture the aggregation and inhibition of amyloid aggregation. These four system-oriented objectives will be accompanied by a technological objective, (5) aimed at implementing improvements in terms of dynamic range and resolution of iSCAMS required for studying self-assembly. As a consequence of the universal applicability of our approach for characterising molecular interactions, oligomeric distributions and dynamics in a facile fashion in solution, this ambitious project opens up a broad range of exciting applications beyond molecular biophysics in fields as drug-discovery, bioanalytical and biomedical science.
Max ERC Funding
1 999 574 €
Duration
Start date: 2019-06-01, End date: 2024-05-31
Project acronym PoliticsOfPatents
Project Politics of Patents: Re-imagining citizenship via clothing inventions 1820 - 2020
Researcher (PI) Katrina Elly JUNGNICKEL
Host Institution (HI) GOLDSMITHS' COLLEGE
Country United Kingdom
Call Details Consolidator Grant (CoG), SH3, ERC-2018-COG
Summary From Victorian women cyclists, who suffered social stigma for daring to replace their skirts with bloomers a century ago, to the recent French burkini ban, where women were forcibly removed from beaches, specifically clothed bodies have long been sites of debate about gender, race, class and religion in public space. Clothing is directly connected to social life and the political world and as such is central to ideas around the politics of identity, participation and belonging. Yet, it is under explored in relation to citizenship studies. This five-year project undertakes for the first time a transnational sociological investigation of 200 years of clothing inventions. It focuses on clothing patents in Espacenet, the European Patent Office’s free online database. Inventors are the focus as they operate on the cutting edge of social and political change; building on the past to make claims on the present and imagine different futures. Central to this research is the idea that clothing inventors can be explored as citizen-makers and that clothing patents are rich untapped sources of data that render visible alternative citizenship possibilities, which may provoke new questions about things we take for granted. The research will be located in a Patent Lab using an inventive mixed-methods approach including quantitative and in-depth visual and document analysis, interviews with inventors and garment reconstruction.
Summary
From Victorian women cyclists, who suffered social stigma for daring to replace their skirts with bloomers a century ago, to the recent French burkini ban, where women were forcibly removed from beaches, specifically clothed bodies have long been sites of debate about gender, race, class and religion in public space. Clothing is directly connected to social life and the political world and as such is central to ideas around the politics of identity, participation and belonging. Yet, it is under explored in relation to citizenship studies. This five-year project undertakes for the first time a transnational sociological investigation of 200 years of clothing inventions. It focuses on clothing patents in Espacenet, the European Patent Office’s free online database. Inventors are the focus as they operate on the cutting edge of social and political change; building on the past to make claims on the present and imagine different futures. Central to this research is the idea that clothing inventors can be explored as citizen-makers and that clothing patents are rich untapped sources of data that render visible alternative citizenship possibilities, which may provoke new questions about things we take for granted. The research will be located in a Patent Lab using an inventive mixed-methods approach including quantitative and in-depth visual and document analysis, interviews with inventors and garment reconstruction.
Max ERC Funding
1 802 154 €
Duration
Start date: 2019-03-01, End date: 2024-02-29
Project acronym ProDAP
Project Protein Dynamics in Antiviral Processes
Researcher (PI) Andreas PICHLMAIR
Host Institution (HI) TECHNISCHE UNIVERSITAET MUENCHEN
Country Germany
Call Details Consolidator Grant (CoG), LS6, ERC-2018-COG
Summary The innate antiviral defense system is of central importance to protect from viral pathogens. Its ability to mitigate a detrimental outcome of an infectious event relies on interactions that happen between viral and host-derived proteins as well as on signalling cascades that regulate the cellular response. However, despite the importance of these interactions, the involved processes and proteins are not yet fully understood.
We established state of the art mass spectrometry techniques and statistical modelling to characterise protein-protein interactions that are affected by viruses. We identified a class of proteins we name “viral affected proteins changing their interaction” (iVAPs). In addition, we established protein turnover rates of >6900 proteins in virus infected cells and identified a group of “viral affected proteins changing turnover rates” (tVAPs). tVAPs are regulated on basis of protein stabilisation, degradation or translation. Preliminary experiments show critical importance of iVAPs and tVAPs in antiviral immunity, suggesting functional similarities to Interferon stimulated genes (ISGs). Alike ISGs, VAPs therefore represent a critical component of the immune system.
ProDAP will establish the function of iVAPs and tVAPs in the antiviral immune response. Systematic screens employing depletion and overexpression experiments, integration of these data in functional networks and mechanistic follow up studies will be performed. Already identified and new candidate proteins will be tested mechanistically for their immune-regulatory capacity and their influence on virus infections in vitro and in vivo.
ProDAP will allow insights in yet unstudied modulators of host-pathogen interplay and will influence our current understanding of immune regulation in general. It is well established that ISGs are of central importance to defend virus infections and we hypothesize that VAPs may fulfil a similarly important protective function that has yet not been elucid
Summary
The innate antiviral defense system is of central importance to protect from viral pathogens. Its ability to mitigate a detrimental outcome of an infectious event relies on interactions that happen between viral and host-derived proteins as well as on signalling cascades that regulate the cellular response. However, despite the importance of these interactions, the involved processes and proteins are not yet fully understood.
We established state of the art mass spectrometry techniques and statistical modelling to characterise protein-protein interactions that are affected by viruses. We identified a class of proteins we name “viral affected proteins changing their interaction” (iVAPs). In addition, we established protein turnover rates of >6900 proteins in virus infected cells and identified a group of “viral affected proteins changing turnover rates” (tVAPs). tVAPs are regulated on basis of protein stabilisation, degradation or translation. Preliminary experiments show critical importance of iVAPs and tVAPs in antiviral immunity, suggesting functional similarities to Interferon stimulated genes (ISGs). Alike ISGs, VAPs therefore represent a critical component of the immune system.
ProDAP will establish the function of iVAPs and tVAPs in the antiviral immune response. Systematic screens employing depletion and overexpression experiments, integration of these data in functional networks and mechanistic follow up studies will be performed. Already identified and new candidate proteins will be tested mechanistically for their immune-regulatory capacity and their influence on virus infections in vitro and in vivo.
ProDAP will allow insights in yet unstudied modulators of host-pathogen interplay and will influence our current understanding of immune regulation in general. It is well established that ISGs are of central importance to defend virus infections and we hypothesize that VAPs may fulfil a similarly important protective function that has yet not been elucid
Max ERC Funding
2 169 555 €
Duration
Start date: 2019-04-01, End date: 2024-03-31
Project acronym ROSA
Project Religion and Its Others in South Asia and the World: Communities, Debates, Freedoms
Researcher (PI) Jacob COPEMAN
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Country United Kingdom
Call Details Consolidator Grant (CoG), SH3, ERC-2018-COG
Summary Those who question or do not conform to dominant local religious tradition(s) and/or religion as such have, of course, faced serious problems and difficulties in a number of different historical periods and locations. This project examines the forms in which individuals and communities raise, in the open or in more hidden transcripts, questions over the dominant religious norms in South Asia. This project is also interested in how such people are being targeted as distinct minorities by various religious and political groups. However, the effects of these encounters extend beyond this region: a significant number of community members now seek asylum in European countries. In consequence, these countries are now debating whether, or to what extent, varieties of religious non-conformism can be legitimate reasons for granting asylum.
While much recent academic work has focused on religious revivalism and reformist movements, critical engagement and sceptical attitudes towards dominant religious norms in South Asia are so far under-researched. A key aim of this study is to correct this absence and thereby to transform our understanding of the kinds of positions, individuals and communities that flourish but also, and critically, face challenges and provoke social contentions in South Asia. It will provide three national ‘deep contextualisations’ of debates and criticism faced by secularists and religious sceptics in South Asia, asking: What are the specific circumstances in which criticism targeting these communities and positions evolve? This study also investigates the assumptions that inform European countries’ responses to cases in which asylum is sought on the basis of claimants’ religious nonconformism, and also those informing advocacy work performed by global secular networks on their behalf. Thus, while this project is ethnographically grounded in South Asia, it also extends beyond this region to examine global implications of critical debates and actions that are taking place there.
Summary
Those who question or do not conform to dominant local religious tradition(s) and/or religion as such have, of course, faced serious problems and difficulties in a number of different historical periods and locations. This project examines the forms in which individuals and communities raise, in the open or in more hidden transcripts, questions over the dominant religious norms in South Asia. This project is also interested in how such people are being targeted as distinct minorities by various religious and political groups. However, the effects of these encounters extend beyond this region: a significant number of community members now seek asylum in European countries. In consequence, these countries are now debating whether, or to what extent, varieties of religious non-conformism can be legitimate reasons for granting asylum.
While much recent academic work has focused on religious revivalism and reformist movements, critical engagement and sceptical attitudes towards dominant religious norms in South Asia are so far under-researched. A key aim of this study is to correct this absence and thereby to transform our understanding of the kinds of positions, individuals and communities that flourish but also, and critically, face challenges and provoke social contentions in South Asia. It will provide three national ‘deep contextualisations’ of debates and criticism faced by secularists and religious sceptics in South Asia, asking: What are the specific circumstances in which criticism targeting these communities and positions evolve? This study also investigates the assumptions that inform European countries’ responses to cases in which asylum is sought on the basis of claimants’ religious nonconformism, and also those informing advocacy work performed by global secular networks on their behalf. Thus, while this project is ethnographically grounded in South Asia, it also extends beyond this region to examine global implications of critical debates and actions that are taking place there.
Max ERC Funding
1 999 782 €
Duration
Start date: 2019-12-01, End date: 2024-11-30
Project acronym RUSINFORM
Project The Consequences of the Internet for Russia's Informational Influence Abroad
Researcher (PI) Florian TOEPFL
Host Institution (HI) UNIVERSITAT PASSAU
Country Germany
Call Details Consolidator Grant (CoG), SH3, ERC-2018-COG
Summary Over the past decade, Russia’s ruling elites have massively stepped up their efforts to influ-ence media audiences abroad. Amongst others, Russia has been alleged to have sought to sway votes in Austria, France, Germany, Ukraine, and the US. This project’s overarching research ques-tion is: How, and with what consequences, have new Internet-based technologies contributed to the emergence of novel resources, techniques, and processes by which political elites in Moscow can influence media audiences abroad?
In order to address this question, a theoretical work package (WP4) will undertake the first major systematic effort to interrogate how much, or how little, we can leverage extant in-depth knowledge of former-Soviet foreign propaganda, conducted in the broadcast era, in order to make sense of Russia’s recent digitally-enabled efforts.
WP4 will be informed by three empirical WPs. They will scrutinize three heavily digitally-enabled elements of Russia’s recent efforts:
• WP1 will conduct the first in-depth study of the foreign online audiences who co-create and disseminate Russia-related content.
• WP2 will produce pioneering research about how social media platforms function as key transmission channels that connect Russia’s domestic media with Russian-speaking audiences abroad.
• WP3 will be the first study to scrutinize the role of the Kremlin-controlled search engine Yan-dex as a resource of foreign influence.
Methodologically, WP1-3 are highly innovative because they combine new computational methods (data mining, automated text analysis) with traditional methods (surveys, in-depth inter-views, grounded theory).
In response to Russia’s recent efforts, countermeasures have been ushered in by a plurality of actors, including the EU, NATO, and NGOs. These actors will benefit immensely from the knowledge generated, which will enable them to enhance their initiatives to secure democratic elec-toral processes against undue informational interference.
Summary
Over the past decade, Russia’s ruling elites have massively stepped up their efforts to influ-ence media audiences abroad. Amongst others, Russia has been alleged to have sought to sway votes in Austria, France, Germany, Ukraine, and the US. This project’s overarching research ques-tion is: How, and with what consequences, have new Internet-based technologies contributed to the emergence of novel resources, techniques, and processes by which political elites in Moscow can influence media audiences abroad?
In order to address this question, a theoretical work package (WP4) will undertake the first major systematic effort to interrogate how much, or how little, we can leverage extant in-depth knowledge of former-Soviet foreign propaganda, conducted in the broadcast era, in order to make sense of Russia’s recent digitally-enabled efforts.
WP4 will be informed by three empirical WPs. They will scrutinize three heavily digitally-enabled elements of Russia’s recent efforts:
• WP1 will conduct the first in-depth study of the foreign online audiences who co-create and disseminate Russia-related content.
• WP2 will produce pioneering research about how social media platforms function as key transmission channels that connect Russia’s domestic media with Russian-speaking audiences abroad.
• WP3 will be the first study to scrutinize the role of the Kremlin-controlled search engine Yan-dex as a resource of foreign influence.
Methodologically, WP1-3 are highly innovative because they combine new computational methods (data mining, automated text analysis) with traditional methods (surveys, in-depth inter-views, grounded theory).
In response to Russia’s recent efforts, countermeasures have been ushered in by a plurality of actors, including the EU, NATO, and NGOs. These actors will benefit immensely from the knowledge generated, which will enable them to enhance their initiatives to secure democratic elec-toral processes against undue informational interference.
Max ERC Funding
1 999 535 €
Duration
Start date: 2019-11-01, End date: 2024-10-31
Project acronym STEP 2
Project Spatiotemporal regulation of T-cell Priming
Researcher (PI) Wolfgang Kastenmueller
Host Institution (HI) JULIUS-MAXIMILIANS-UNIVERSITAT WURZBURG
Country Germany
Call Details Consolidator Grant (CoG), LS6, ERC-2018-COG
Summary The initiation of adaptive cellular immunity requires antigen-specific interactions between Dendritic cells (DC) and naive CD8 T cells in secondary lymphoid organs. We aim to understand how the dynamic migratory behavior of myeloid and lymphoid cells is coordinated to ensure that “the right cells” communicate at “the right time” in “the right place” to enable robust immune responses. Using intravital microscopy, we have recently identified a critical phase (“Step 2”) of T cell priming that follows the initial encounter of DC and CD8 T cells and is essential to develop protective immunity.
The aim of this proposal is to identify the cellular and molecular mechanisms regulating T cell differentiation during Step 2. We will employ a newly developed imaging method (“Net-Vis”) to investigate how key elements of Step 2 (XCR1 DC) receive antigenic and inflammatory “information” within a network of myeloid cells. Next, we will test a novel model of T cell priming in which stepwise relocalization to multicellular clusters within the LN orchestrates T cell differentiation. Combining deep-tissue intravital microscopy, “Niche-seq” and novel genetic approaches, we will identify the cellular players and molecules guiding these processes and test their mechanistic implications. Finally, we will investigate the identity and mechanisms of Foxp3+ T cells that co-regulate CD8 T cell activation and differentiation during Step 2.
In summary, we will exploit an array of innovative imaging, spatiotemporal transcriptomics and genetic approaches to investigate novel fundamental aspects of CD8 T cell priming during a newly discovered distinct phase of T cell activation and differentiation. Investigating the mechanisms that guide these central steps in adaptive immunity is anticipated to reveal new avenues for the therapeutic manipulation of immune responses against infection and cancer.
Summary
The initiation of adaptive cellular immunity requires antigen-specific interactions between Dendritic cells (DC) and naive CD8 T cells in secondary lymphoid organs. We aim to understand how the dynamic migratory behavior of myeloid and lymphoid cells is coordinated to ensure that “the right cells” communicate at “the right time” in “the right place” to enable robust immune responses. Using intravital microscopy, we have recently identified a critical phase (“Step 2”) of T cell priming that follows the initial encounter of DC and CD8 T cells and is essential to develop protective immunity.
The aim of this proposal is to identify the cellular and molecular mechanisms regulating T cell differentiation during Step 2. We will employ a newly developed imaging method (“Net-Vis”) to investigate how key elements of Step 2 (XCR1 DC) receive antigenic and inflammatory “information” within a network of myeloid cells. Next, we will test a novel model of T cell priming in which stepwise relocalization to multicellular clusters within the LN orchestrates T cell differentiation. Combining deep-tissue intravital microscopy, “Niche-seq” and novel genetic approaches, we will identify the cellular players and molecules guiding these processes and test their mechanistic implications. Finally, we will investigate the identity and mechanisms of Foxp3+ T cells that co-regulate CD8 T cell activation and differentiation during Step 2.
In summary, we will exploit an array of innovative imaging, spatiotemporal transcriptomics and genetic approaches to investigate novel fundamental aspects of CD8 T cell priming during a newly discovered distinct phase of T cell activation and differentiation. Investigating the mechanisms that guide these central steps in adaptive immunity is anticipated to reveal new avenues for the therapeutic manipulation of immune responses against infection and cancer.
Max ERC Funding
1 874 425 €
Duration
Start date: 2019-09-01, End date: 2024-08-31
Project acronym TRIFECTs
Project Trions and sp3-Defects in Single-walled Carbon Nanotubes for Optoelectronics
Researcher (PI) Jana ZAUMSEIL
Host Institution (HI) RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG
Country Germany
Call Details Consolidator Grant (CoG), PE4, ERC-2018-COG
Summary Semiconducting single-walled carbon nanotubes (SWNTs) combine solution-processability, large carrier mobilities, narrow emission linewidths and environmental stability for optoelectronic devices with light-emission in the near-infrared (800-1800 nm, e.g., for optical data communication and bio-imaging) when sorted by (n,m) species. The recent availability of highly pure, monochiral semiconducting SWNTs as bulk materials allows us to employ and further tailor their charge transport and light emission properties and thus enables their application in practical devices. Two new emissive species - charged excitons (trions) and bright sp3-defects - were recently discovered in SWNTs and have fundamentally changed our notions about SWNT luminescence. Both show red-shifted, narrow and enhanced emission. However, very little is yet known about their photophysical properties and especially their interactions with each other and their environment (e.g., in devices). Their emissive properties could potentially be tailored by external magnetic fields, dielectric environment and additional functional groups. Strong light-matter coupling in suitable optical cavities could be applied to create trion-polaritons in SWNTs as new low-mass charge carriers in polaritonic devices. Trions and emissive sp3-defects are not limited to SWNTs and hence these concepts could be transferred and applied to other low-dimensional semiconductors.
The goals of this project are to
- understand and use trions and trion-polaritons for light emission and polaritonic charge transport,
- understand and tune the interactions of sp3-defects with charges and trions in SWNTs,
- modify and apply sp3-defects for enhanced light emission from SWNTs in optoelectronic devices,
- explore trions in new low-dimensional materials (e.g., graphene nanoribbons and novel monolayered semiconductors).
Summary
Semiconducting single-walled carbon nanotubes (SWNTs) combine solution-processability, large carrier mobilities, narrow emission linewidths and environmental stability for optoelectronic devices with light-emission in the near-infrared (800-1800 nm, e.g., for optical data communication and bio-imaging) when sorted by (n,m) species. The recent availability of highly pure, monochiral semiconducting SWNTs as bulk materials allows us to employ and further tailor their charge transport and light emission properties and thus enables their application in practical devices. Two new emissive species - charged excitons (trions) and bright sp3-defects - were recently discovered in SWNTs and have fundamentally changed our notions about SWNT luminescence. Both show red-shifted, narrow and enhanced emission. However, very little is yet known about their photophysical properties and especially their interactions with each other and their environment (e.g., in devices). Their emissive properties could potentially be tailored by external magnetic fields, dielectric environment and additional functional groups. Strong light-matter coupling in suitable optical cavities could be applied to create trion-polaritons in SWNTs as new low-mass charge carriers in polaritonic devices. Trions and emissive sp3-defects are not limited to SWNTs and hence these concepts could be transferred and applied to other low-dimensional semiconductors.
The goals of this project are to
- understand and use trions and trion-polaritons for light emission and polaritonic charge transport,
- understand and tune the interactions of sp3-defects with charges and trions in SWNTs,
- modify and apply sp3-defects for enhanced light emission from SWNTs in optoelectronic devices,
- explore trions in new low-dimensional materials (e.g., graphene nanoribbons and novel monolayered semiconductors).
Max ERC Funding
1 998 500 €
Duration
Start date: 2019-04-01, End date: 2024-03-31