Project acronym STANIB
Project Space, Time and Number In the Brain
Researcher (PI) David Burr
Host Institution (HI) UNIVERSITA DEGLI STUDI DI FIRENZE
Call Details Advanced Grant (AdG), SH4, ERC-2008-AdG
Summary The primary aim of this project is to establish in Pisa a European Centre of Excellence dedicated to frontier, interdisciplinary research of human perception. The research will focus primarily on the human visual system (and its development), but will also investigate key issues of cross-sensory integration. The Institute of Neuroscience has been a leading centre of visual research since its inception in the 1970s, when the multidisciplinary approach of Lamberto Maffei (physiologist) and Adriana Fiorentini (psychophysicist) made seminal and highly influential contributions to many aspects of human and animal vision. In recent years, the focus of the institute has veered towards developmental neurobiology. This project aims to reestablish a cognitive visual neuroscience section within the institute, dedicated to multidisciplinary research into human perception, using modern, non-invasive experimental techniques, such as psychophysics, evoked potentials, neuro-imaging and neuro-computation. The PI has been highly active in cognitive visual neuroscience for thirty years, publishing 150 publications on diverse aspects of perception, including motion perception, colour, space, and vision during saccadics. The planned research builds on these themes, aiming at achieving a firmer understanding of perceptual processes. New topics will also be tackled, such as cross-modal integration between the senses, the perception of event duration and the sense of number estimation, or numerosity. The research will be multi-disciplinary, using psychophysical, neuro-computational and neuro-imaging techniques. Particularly exciting will be the application of state-of-the-art high-field imaging to these important research questions. The establishment of this centre would be fundamental for Italian and European neuroscience in providing a laboratory of critical mass to focus the existing expertise, and to train young scientists within a long-standing tradition of excellence.
Summary
The primary aim of this project is to establish in Pisa a European Centre of Excellence dedicated to frontier, interdisciplinary research of human perception. The research will focus primarily on the human visual system (and its development), but will also investigate key issues of cross-sensory integration. The Institute of Neuroscience has been a leading centre of visual research since its inception in the 1970s, when the multidisciplinary approach of Lamberto Maffei (physiologist) and Adriana Fiorentini (psychophysicist) made seminal and highly influential contributions to many aspects of human and animal vision. In recent years, the focus of the institute has veered towards developmental neurobiology. This project aims to reestablish a cognitive visual neuroscience section within the institute, dedicated to multidisciplinary research into human perception, using modern, non-invasive experimental techniques, such as psychophysics, evoked potentials, neuro-imaging and neuro-computation. The PI has been highly active in cognitive visual neuroscience for thirty years, publishing 150 publications on diverse aspects of perception, including motion perception, colour, space, and vision during saccadics. The planned research builds on these themes, aiming at achieving a firmer understanding of perceptual processes. New topics will also be tackled, such as cross-modal integration between the senses, the perception of event duration and the sense of number estimation, or numerosity. The research will be multi-disciplinary, using psychophysical, neuro-computational and neuro-imaging techniques. Particularly exciting will be the application of state-of-the-art high-field imaging to these important research questions. The establishment of this centre would be fundamental for Italian and European neuroscience in providing a laboratory of critical mass to focus the existing expertise, and to train young scientists within a long-standing tradition of excellence.
Max ERC Funding
2 376 000 €
Duration
Start date: 2009-07-01, End date: 2014-06-30
Project acronym STIMULUS
Project Space-Time Methods for Multi-Fluid Problems on Unstructured Meshes
Researcher (PI) Michael Dumbser
Host Institution (HI) UNIVERSITA DEGLI STUDI DI TRENTO
Call Details Starting Grant (StG), PE1, ERC-2011-StG_20101014
Summary In this project we develop new algorithms for the solution of general nonlinear systems of time dependent partial differential equations (PDE) in the context of non-ideal magnetized multi-fluid plasma flows with thermal radiation. We will produce new high order schemes on unstructured tetrahedral meshes that are applicable to a rather general class of problems in general geometries, thus opening a wide range of possible applications in science and engineering. We will consider both, Eulerian methods on fixed grids and Lagrangian schemes on moving meshes to reduce numerical diffusion at material interfaces. A particular feature of our schemes is that they are high-order one-step methods based on local space-time predictors that allow using time-accurate local time stepping, i.e. each element runs at its own optimal time step. Even nowadays better than second order accurate 3D unstructured Eulerian methods are very rare, but there is still no better than second order accurate unstructured Lagrangian scheme available on general tetrahedral meshes. To develop these missing algorithms is the objective of our research project.
A very challenging application that we have in mind is inertial confinement fusion (ICF) which is highly relevant for modern society and its increasing need for clean and inexhaustible energy. It is believed that early ICF experiments in the 1970ies failed because they did not reach the necessary critical pressure and temperature due to hydrodynamic instabilities in the flow. In this project we propose to design algorithms for simulating ICF flows with billions of high order elements on up to 100,000 CPUs of modern supercomputers. We will also propose active control strategies based on adjoint equations to reduce the hydrodynamical instabilities. Hence this project aims at providing next-generation numerical modeling tools for a possible future scenario of clean civil energy production via ICF.
Summary
In this project we develop new algorithms for the solution of general nonlinear systems of time dependent partial differential equations (PDE) in the context of non-ideal magnetized multi-fluid plasma flows with thermal radiation. We will produce new high order schemes on unstructured tetrahedral meshes that are applicable to a rather general class of problems in general geometries, thus opening a wide range of possible applications in science and engineering. We will consider both, Eulerian methods on fixed grids and Lagrangian schemes on moving meshes to reduce numerical diffusion at material interfaces. A particular feature of our schemes is that they are high-order one-step methods based on local space-time predictors that allow using time-accurate local time stepping, i.e. each element runs at its own optimal time step. Even nowadays better than second order accurate 3D unstructured Eulerian methods are very rare, but there is still no better than second order accurate unstructured Lagrangian scheme available on general tetrahedral meshes. To develop these missing algorithms is the objective of our research project.
A very challenging application that we have in mind is inertial confinement fusion (ICF) which is highly relevant for modern society and its increasing need for clean and inexhaustible energy. It is believed that early ICF experiments in the 1970ies failed because they did not reach the necessary critical pressure and temperature due to hydrodynamic instabilities in the flow. In this project we propose to design algorithms for simulating ICF flows with billions of high order elements on up to 100,000 CPUs of modern supercomputers. We will also propose active control strategies based on adjoint equations to reduce the hydrodynamical instabilities. Hence this project aims at providing next-generation numerical modeling tools for a possible future scenario of clean civil energy production via ICF.
Max ERC Funding
918 000 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym STRATUS
Project Structure and dynamics of biomolecules by two-dimensional ultraviolet spectroscopy
Researcher (PI) Giulio Cerullo
Host Institution (HI) POLITECNICO DI MILANO
Call Details Advanced Grant (AdG), PE4, ERC-2011-ADG_20110209
Summary "Two-dimensional (2D) nuclear magnetic resonance is a diagnostic technique that has revolutionized structural biology. A wealth of spectroscopic information can be obtained by extrapolating 2D techniques to the optical frequency domain, using ultrashort light pulses. 2D electronic spectroscopy (2DES) allows fundamentally new insights into the structure and dynamics of multi-chromophore systems, by measuring how the electronic states of chromophores interact with one another and transfer electronic excitations. Due to technical difficulties, 2DES has been limited so far to the visible range, while most biomolecules absorb in the ultraviolet (UV). This project aims at extending 2DES to the challenging and still uncharted UV-domain and applying it to the study of the photophysics of genomic systems and of the secondary structure of proteins.
Nature has engineered DNA molecules to be photostable, so that harmful photochemical processes are minimized. 2DES will unravel the molecular mechanisms of the photoinduced electronic intra/inter-chromophore events in DNA, exposing the energy dissipation pathways which are responsible for its photoprotection.
2DES will be also established as a new diagnostic tool for structural studies of polypeptides and proteins, relying on the UV absorbing peptide bonds and aromatic residues, the latter acting as native local structural probes. 2DES will provide sensitive information on the misfolding/aggregation processes responsible for a wide class of diseases, with the speed of standard optical techniques but with a much greater information content. This will bridge the experimental gap between crude estimates of protein unfolding and full structure determination, enabling rapid assessment of which variants are worth of deeper structural studies.
To realize the full power of 2DES, experiments will be combined with simulations and electronic calculations that are necessary to correlate the data with molecular states and structures."
Summary
"Two-dimensional (2D) nuclear magnetic resonance is a diagnostic technique that has revolutionized structural biology. A wealth of spectroscopic information can be obtained by extrapolating 2D techniques to the optical frequency domain, using ultrashort light pulses. 2D electronic spectroscopy (2DES) allows fundamentally new insights into the structure and dynamics of multi-chromophore systems, by measuring how the electronic states of chromophores interact with one another and transfer electronic excitations. Due to technical difficulties, 2DES has been limited so far to the visible range, while most biomolecules absorb in the ultraviolet (UV). This project aims at extending 2DES to the challenging and still uncharted UV-domain and applying it to the study of the photophysics of genomic systems and of the secondary structure of proteins.
Nature has engineered DNA molecules to be photostable, so that harmful photochemical processes are minimized. 2DES will unravel the molecular mechanisms of the photoinduced electronic intra/inter-chromophore events in DNA, exposing the energy dissipation pathways which are responsible for its photoprotection.
2DES will be also established as a new diagnostic tool for structural studies of polypeptides and proteins, relying on the UV absorbing peptide bonds and aromatic residues, the latter acting as native local structural probes. 2DES will provide sensitive information on the misfolding/aggregation processes responsible for a wide class of diseases, with the speed of standard optical techniques but with a much greater information content. This will bridge the experimental gap between crude estimates of protein unfolding and full structure determination, enabling rapid assessment of which variants are worth of deeper structural studies.
To realize the full power of 2DES, experiments will be combined with simulations and electronic calculations that are necessary to correlate the data with molecular states and structures."
Max ERC Funding
2 493 000 €
Duration
Start date: 2012-04-01, End date: 2017-03-31
Project acronym SULFENIC
Project Unraveling the cellular sulfenome: a search for new redox-regulated pathways
Researcher (PI) Jean-Francois Gaëtan Collet
Host Institution (HI) UNIVERSITE CATHOLIQUE DE LOUVAIN
Call Details Starting Grant (StG), LS1, ERC-2011-StG_20101109
Summary Within proteins, cysteine residues are sensitive to oxidation by reactive oxygen species (ROS). The first oxidation product of cysteines exposed to ROS is the sulfenic acid derivative (-SOH). Sulfenic acids are highly reactive intermediates that, unless they are stabilized within the protein microenvironment, react with another cysteine present in the vicinity to form a disulfide or are further oxidized to the irreversible sulfinic (-SO2H) and sulfonic (-SO3H) acid modifications. Sulfenic acid formation has traditionally been viewed as an unwanted reaction opening the way to damages that are harmful to proteins. However, it has become clear in recent years that formation of sulfenic acids is not always deleterious to the cell. A new concept is emerging, in which sulfenylation of specific cysteine residues modulates signal transduction pathways by altering the activity and function of cellular proteins, just as phosphorylation and dephosphorylation cycles regulate enzyme activities and cellular pathways. However, the modulation of protein function by sulfenic acid formation has been unambiguously shown for only a few proteins. We postulate that specific oxidation of cysteine residues via sulfenylation modulates the activity of many more proteins and pathways and that numerous sulfenylation sites have not yet been recognized. We want to apply an unprecedented multi-facetted approach to fully grasp the physiological scope of cysteine sulfenic acid formation by uncovering the sulfenome of a living organism, using Escherichia coli as a model. The main objectives of our research program are (1) to comprehensively characterize the sulfenome of E. coli, 2) to identify new proteins and pathways regulated by sulfenylation and (3) to understand how sulfenyla-tion is controlled at the cellular level. If our hypothesis proves to be true, our project will uncover a new “redox dimension” affecting many cellular processes and pathways, opening up new avenues of investigation.
Summary
Within proteins, cysteine residues are sensitive to oxidation by reactive oxygen species (ROS). The first oxidation product of cysteines exposed to ROS is the sulfenic acid derivative (-SOH). Sulfenic acids are highly reactive intermediates that, unless they are stabilized within the protein microenvironment, react with another cysteine present in the vicinity to form a disulfide or are further oxidized to the irreversible sulfinic (-SO2H) and sulfonic (-SO3H) acid modifications. Sulfenic acid formation has traditionally been viewed as an unwanted reaction opening the way to damages that are harmful to proteins. However, it has become clear in recent years that formation of sulfenic acids is not always deleterious to the cell. A new concept is emerging, in which sulfenylation of specific cysteine residues modulates signal transduction pathways by altering the activity and function of cellular proteins, just as phosphorylation and dephosphorylation cycles regulate enzyme activities and cellular pathways. However, the modulation of protein function by sulfenic acid formation has been unambiguously shown for only a few proteins. We postulate that specific oxidation of cysteine residues via sulfenylation modulates the activity of many more proteins and pathways and that numerous sulfenylation sites have not yet been recognized. We want to apply an unprecedented multi-facetted approach to fully grasp the physiological scope of cysteine sulfenic acid formation by uncovering the sulfenome of a living organism, using Escherichia coli as a model. The main objectives of our research program are (1) to comprehensively characterize the sulfenome of E. coli, 2) to identify new proteins and pathways regulated by sulfenylation and (3) to understand how sulfenyla-tion is controlled at the cellular level. If our hypothesis proves to be true, our project will uncover a new “redox dimension” affecting many cellular processes and pathways, opening up new avenues of investigation.
Max ERC Funding
1 492 000 €
Duration
Start date: 2011-11-01, End date: 2016-10-31
Project acronym SYMBIOVEC
Project Yeast symbionts of malaria vectors: from basic research to the management of malaria control
Researcher (PI) Irene Ricci
Host Institution (HI) UNIVERSITA DEGLI STUDI DI CAMERINO
Call Details Starting Grant (StG), LS9, ERC-2011-StG_20101109
Summary Advances in biotechnology propose innovative tools particularly relevant for public health application by genetic manipulation of microbial symbionts of arthropod vectoring disease. The symbiont engineering prevents the transmission of pathogens to human by interfering with their stage within the arthropod, thorough the expression of anti-pathogen effector molecules. This approach, defined paratransgenesis is simpler than the proposed engineering of the vector itself (transgenesis) and implies minor applicative and ethical concerns. Identification of good candidate for paratransgenesis has opened the way towards the investigation of microbes residing in the arthropod body, particularly those localised within the gut that often represents the locale in which pathogens transit or develop. Good paratransgenic candidates were already identified in the bug vectoring Chagas disease in South America and in the tse-tse fly vectoring sleeping sickness in Africa. As regard mosquitoes, responsible of tens of human infections including malaria, some interesting bacteria have been recognized as candidates for genetic manipulation, even if the ability of recombinant strains to cure mosquito has not been demonstrated yet in the field. Bacteria can be easily isolated, modified and reintroduced in the mosquito but secretion of antagonists by prokaryotic cell can represent a matter difficult to resolve. In this context endosymbiotic yeasts seem to be very appealing. Their genetic and cellular complexity makes yeasts as ideal tools for manipulation and bypasses many difficulties relative to the recombinant products releasing. On these bases, I have recently begun a study on the yeast microflora in mosquito. Particularly, I investigated the relationship between the yeast endosymbiont Pichia anomala and malaria vectors. Considering the special features of this yeast, I propose its use as paratransgenic tool for malaria control.
Summary
Advances in biotechnology propose innovative tools particularly relevant for public health application by genetic manipulation of microbial symbionts of arthropod vectoring disease. The symbiont engineering prevents the transmission of pathogens to human by interfering with their stage within the arthropod, thorough the expression of anti-pathogen effector molecules. This approach, defined paratransgenesis is simpler than the proposed engineering of the vector itself (transgenesis) and implies minor applicative and ethical concerns. Identification of good candidate for paratransgenesis has opened the way towards the investigation of microbes residing in the arthropod body, particularly those localised within the gut that often represents the locale in which pathogens transit or develop. Good paratransgenic candidates were already identified in the bug vectoring Chagas disease in South America and in the tse-tse fly vectoring sleeping sickness in Africa. As regard mosquitoes, responsible of tens of human infections including malaria, some interesting bacteria have been recognized as candidates for genetic manipulation, even if the ability of recombinant strains to cure mosquito has not been demonstrated yet in the field. Bacteria can be easily isolated, modified and reintroduced in the mosquito but secretion of antagonists by prokaryotic cell can represent a matter difficult to resolve. In this context endosymbiotic yeasts seem to be very appealing. Their genetic and cellular complexity makes yeasts as ideal tools for manipulation and bypasses many difficulties relative to the recombinant products releasing. On these bases, I have recently begun a study on the yeast microflora in mosquito. Particularly, I investigated the relationship between the yeast endosymbiont Pichia anomala and malaria vectors. Considering the special features of this yeast, I propose its use as paratransgenic tool for malaria control.
Max ERC Funding
1 500 000 €
Duration
Start date: 2012-06-01, End date: 2017-05-31
Project acronym VORTEX
Project Exploring electron vortex beams
Researcher (PI) Johan Verbeeck
Host Institution (HI) UNIVERSITEIT ANTWERPEN
Call Details Starting Grant (StG), PE3, ERC-2011-StG_20101014
Summary In this project I will exploit new possibilities opened up by the recent succesful demonstration of our ability to create electron vortex beams in a transmission electron microscope. Electron vortex beams carry a helical phase and angular momentum around their propagation axis. They form the counterpart of optical vortex beams that were invented almost 20 years ago and have lead to many exciting new applications in optics.
In preliminary experiments with electron vortices I have demonstrated (Verbeeck et al. Nature, 467,301 (2010)) their usefulness for magnetic state mapping. This property makes them very desirable for solid state physics and materials science since no other tool exists that can map the local magnetisation inside materials with atomic scale resolution. We aim to develop atomic resolution magnetic state mapping and apply it to gain insight in spintronics devices as well as in topological insulators. We will follow two routes to this end, one using the combination of electron vortex beams and electron energy loss spectroscopy (EELS) and another making use of the Aharanov Bohm effect in elastic scattering.
Preliminary experiments proof that both routes are feasible and a wealth of interesting physics is ready to be explored.
We will also explore the potential of electron vortex beams to manipulate nanoparticles and transfer angular momentum from the electron beam to these particles. This would open up the road to assemble and create nanoscale devices and to study the fundamental laws that govern the interaction between vortex beams and particles with different physical properties.
I believe that this highly creative and innovative idea, combined with access to a state of the art transmission electron microscope and a young PI with a proven track record is combined into a project proposal entirely in the spirit of the ERC starting grants.
Summary
In this project I will exploit new possibilities opened up by the recent succesful demonstration of our ability to create electron vortex beams in a transmission electron microscope. Electron vortex beams carry a helical phase and angular momentum around their propagation axis. They form the counterpart of optical vortex beams that were invented almost 20 years ago and have lead to many exciting new applications in optics.
In preliminary experiments with electron vortices I have demonstrated (Verbeeck et al. Nature, 467,301 (2010)) their usefulness for magnetic state mapping. This property makes them very desirable for solid state physics and materials science since no other tool exists that can map the local magnetisation inside materials with atomic scale resolution. We aim to develop atomic resolution magnetic state mapping and apply it to gain insight in spintronics devices as well as in topological insulators. We will follow two routes to this end, one using the combination of electron vortex beams and electron energy loss spectroscopy (EELS) and another making use of the Aharanov Bohm effect in elastic scattering.
Preliminary experiments proof that both routes are feasible and a wealth of interesting physics is ready to be explored.
We will also explore the potential of electron vortex beams to manipulate nanoparticles and transfer angular momentum from the electron beam to these particles. This would open up the road to assemble and create nanoscale devices and to study the fundamental laws that govern the interaction between vortex beams and particles with different physical properties.
I believe that this highly creative and innovative idea, combined with access to a state of the art transmission electron microscope and a young PI with a proven track record is combined into a project proposal entirely in the spirit of the ERC starting grants.
Max ERC Funding
1 458 300 €
Duration
Start date: 2012-01-01, End date: 2016-12-31
Project acronym WillingToPay
Project Willing to Pay? Testing Institutionalist Theory with Experiments
Researcher (PI) Sven Holger Steinmo
Host Institution (HI) EUROPEAN UNIVERSITY INSTITUTE
Call Details Advanced Grant (AdG), SH2, ERC-2011-ADG_20110406
Summary The project will combine experimental techniques and methodologies with historically informed institutionalist analysis in order to more fully test and explore the relationships between institutions, policy regimes and citizen’s policy choices in different welfare states. The research will extend the current work in experimental economics and cognitive science by designing experiments that are modeled on real world institutions and policy choices in several different countries.
Specifically we will focus on two sets of redistributive policy issues: Taxation and public pensions in four democratic nations: Sweden, Italy, Britain and the United States. The basic point will be to build a series of scenarios that will allow us to test how different institutional contexts frame or shape citizens’ decisions and thereby better understand how they perceive and process different policy choices and trade-offs.
Throughout the study, historical institutionalist country specialists will work intensively with the experiments in each round, so that we can both refine the experiments in ways that can make them more realistic within different national contexts, but equally importantly so that we can build experiments that will test the specific hypotheses generated by these country specialists.
I believe that only when we better understand both what citizens in different polities actually believe about their state, and why, can we build realistic models to understand how their policy systems can be reformed or adapted in the context of the enormous pressures they face today. This research will thus combine the strengths of classical historical institutionalist analysis with recent developments in cognitive and evolutionary science and decision theory.
Summary
The project will combine experimental techniques and methodologies with historically informed institutionalist analysis in order to more fully test and explore the relationships between institutions, policy regimes and citizen’s policy choices in different welfare states. The research will extend the current work in experimental economics and cognitive science by designing experiments that are modeled on real world institutions and policy choices in several different countries.
Specifically we will focus on two sets of redistributive policy issues: Taxation and public pensions in four democratic nations: Sweden, Italy, Britain and the United States. The basic point will be to build a series of scenarios that will allow us to test how different institutional contexts frame or shape citizens’ decisions and thereby better understand how they perceive and process different policy choices and trade-offs.
Throughout the study, historical institutionalist country specialists will work intensively with the experiments in each round, so that we can both refine the experiments in ways that can make them more realistic within different national contexts, but equally importantly so that we can build experiments that will test the specific hypotheses generated by these country specialists.
I believe that only when we better understand both what citizens in different polities actually believe about their state, and why, can we build realistic models to understand how their policy systems can be reformed or adapted in the context of the enormous pressures they face today. This research will thus combine the strengths of classical historical institutionalist analysis with recent developments in cognitive and evolutionary science and decision theory.
Max ERC Funding
2 491 135 €
Duration
Start date: 2012-09-01, End date: 2017-08-31