Project description DEENESFRITPL A new way to study protein dynamics in multicellular environments Studying protein dynamics in a physiological multicellular environment is challenging due to the high variability in protein signalling between individual cells and the sparsity of driver cells responsible for a specific physiological process. The EU-funded E-CTRL project will develop technologies to control target proteins in relevant cell subpopulations, aiming to build causal relationships between proteins and multicellular behaviour in neurobiology. It will study how proteins function in sparsely activated neuronal circuits during certain learning tasks in mice. The findings will shed light on the molecular mechanisms underlying memory and on developing new treatments for brain disorders like epilepsy, depression and autism. Show the project objective Hide the project objective Objective Protein signaling in cells is precisely coordinated in space and time. Molecular chemogenetics, optogenetics, and biosensors have generated a scientific revolution enabling the spatiotemporal codes of protein signaling in single cells. However, it is a great challenge to study protein dynamics in a physiological multicellular environment due to the extensive variability in protein signaling within individual cells, as well as the sparsity of driver cells responsible for a specific physiological process. To build causal relationships between proteins and multi-cellular behavior, we will develop broadly applicable technologies by engineering proteins enabling the control of target proteins with light, exclusively in the relevant driver cell subpopulations. These approaches can be used in any biological field in which protein signaling is critical for multi-cellular behavior, but here we will focus on three different stages of a challenging neurobiology process. Upon sensory experience, for example, by learning a new task, only the subsets of neurons within a corresponding brain region switch to the active state. It is largely unknown how proteins that are activated in these sparsely activated neuronal circuits operate in space and time. Our technologies will enlighten the spatiotemporal dynamics of proteins in active neuron subpopulations responding to certain learning tasks in mice. Understanding such learning neuronal circuit responses at the molecular level will pave the way to develop new therapeutic approaches for brain disorders including epilepsy, depression, and autism spectrum disorders. Fields of science natural sciencesbiological sciencesneurobiologyengineering and technologyelectrical engineering, electronic engineering, information engineeringelectronic engineeringsensorsbiosensorsmedical and health sciencesbasic medicineneurologyepilepsynatural sciencesbiological sciencesbiochemistrybiomoleculesproteinssocial sciencespolitical sciencespolitical transitionsrevolutions Keywords biosensors molecular optogenetics chemical biology protein engineering protein switches engineered allostery neural circuits synaptic plasticity cellular circuits Programme(s) HORIZON.1.1 - European Research Council (ERC) Main Programme Topic(s) ERC-2022-STG - ERC STARTING GRANTS Call for proposal ERC-2022-STG See other projects for this call Funding Scheme ERC - Support for frontier research (ERC) Coordinator KAROLINSKA INSTITUTET Net EU contribution € 1 494 669,00 Address Nobels vag 5 17177 Stockholm Sweden See on map Region Östra Sverige Stockholm Stockholms län Activity type Higher or Secondary Education Establishments Links Contact the organisation Opens in new window Website Opens in new window Participation in EU R&I programmes Opens in new window HORIZON collaboration network Opens in new window Other funding € 0,00
