Project Details
SFB 1286: Quantitative Synaptology
Subject Area
Medicine
Biology
Physics
Biology
Physics
Term
since 2017
Website
Homepage
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 317475864
Synapses are the central information processors in the brain. Their function, efficacy and plasticity are key determinants of all brain functions, and of the corresponding behavioral output. Conversely, aberrant synapse function is the cause of many neurological and psychiatric disorders. Our ultimate objective is to generate a functional virtual synapse, in silico, that covers both the presynaptic and postsynaptic compartments.Over the first funding period we proposed to obtain a wide set of molecular, structural and functional data on a prototypic, averaged model synapse, while only engaging a few computational projects. For the second funding period we envisioned refining these data by further wet-lab experimental work, while at the same time enhancing strongly the computational aspects, by recruiting new computational neuroscience projects into the CRC. Finally, the work will culminate in the third funding period, in which we will rely even more heavily on in silico modelling. We followed this plan closely during the first funding period, and we are “on schedule” with regard to most aspects. We determined the locations of many synaptic organelles and proteins, their copy numbers, their movement rates, their metabolic turnover, several of their post-translational modifications, and their interactomes. We also performed multiple analyses of neuronal and synaptic RNAs and lipids. Finally, we initialized several modeling projects, in which collaborations with experimentalists were employed to provide an understanding of defined synaptic processes.During the second funding period, we will continue our work along these lines, while strongly enhancing the computational aspects. As we proposed in 2017, we more than doubled the number of computational projects, which now address multiple aspects of synaptic transmission, from protein movement and nanoscale organization to long-term dynamics and plasticity. The completion of these projects will place us in an optimal position to establish synapse function models in the third funding period.Our synaptic models will be used to answer questions on synaptic function and dysfunction, and will be extremely important in the context of connectomics efforts, since they will suggest the functional responses of synapses in given connectomes, thereby greatly increasing the functionality of structural connectomes.
DFG Programme
Collaborative Research Centres
Current projects
- A01 - The ultrastructure of synapses in action (Project Head Cooper, Ph.D., Benjamin )
- A02 - Structure of synaptic organelles by X-ray diffraction and imaging (Project Head Salditt, Tim )
- A03 - A dynamic analysis of extracellular matrix (ECM) remodeling as a mechanism of synapse organization and plasticity (Project Head Rizzoli, Ph.D., Silvio-Olivier )
- A04 - Activity-dependent morphological changes at endbulb of Held synapses (Project Head Wichmann, Carolin )
- A05 - Mitochondrial heterogeneity in synapses (Project Head Jakobs, Stefan )
- A06 - Mitochondria function and turnover in synapses (Project Heads Rehling, Peter ; Urlaub, Henning )
- A07 - The organization of the synaptic cytoskeleton (Project Heads D' Este, Elisa ; Hell, Stefan W. )
- A08 - The role of post-translationally modified proteins in synaptic transmission (Project Heads Jahn, Reinhard ; Urlaub, Henning )
- A09 - SUMOylation and Neddylation at Synapses (Project Heads Brose, Nils ; Tirard, Marilyn )
- A11 - Molecular architecture of the presynaptic compartment (Project Head Lipstein-Thoms, Ph.D., Noa )
- A12 - Molecular organization of synaptic vesicles (Project Head Fernandez Busnadiego, Ruben )
- B02 - An in vitro approach to understanding the structure-organizing role of the vesicle cluster (Project Heads Köster, Sarah ; Rizzoli, Ph.D., Silvio-Olivier )
- B04 - In vitro reconstitution of inhibitory GABAergic postsynapses (Project Head Steinem, Claudia )
- B05 - Quantitative molecular physiology of calyceal synapses (Project Head Moser, Tobias )
- B06 - The role of RNA in synapse physiology and neurodegeneration (Project Heads Fischer, André ; Outeiro, Tiago Fleming )
- B08 - Defining cascades of molecular alterations in synucleinopathies during neurodegeneration (Project Head Outeiro, Tiago Fleming )
- B10 - Nanoscale Dynamics and Regulation of Synapsin Condensates (Project Head Milovanovic, Dragomir )
- B11 - Signaling mechanisms of synaptic state transitions in relation to long-term synaptic plasticity (Project Head Schlüter, Oliver M. )
- C01 - The plasticity-dependent spatiotemporal organization of AMPARs and scaffolding proteins (Project Head Tetzlaff, Christian )
- C02 - Release face designs and dynamics tailored for synaptic working memory (Project Head Wolf, Fred )
- C03 - Modelling dendritic spine fluctuations (Project Heads Fauth, Michael ; Wörgötter, Florentin )
- C05 - The synapse as a complex physical environment (Project Head Klumpp, Stefan )
- C06 - Coarse-grained simulation of the role of local environment on presynaptic release: from fusion to fission (Project Head Müller, Marcus )
- C08 - Experimental and theoretical analysis of single active zone function (Project Head Moser, Tobias )
- C09 - Relating the presynaptic vesicle cycle to the information processing function of synaptic plasticity (Project Head Priesemann, Viola )
- C10 - Innovative deep learning approaches enable quantitative analyses of synaptic imaging datasets (Project Head Pape, Constantin )
- Z01 - Central Tasks (Project Head Rizzoli, Ph.D., Silvio-Olivier )
- Z02 - Integrative data analysis and interpretation, and generation of a synaptic integrative data strategy (SynIDs) (Project Head Bonn, Stefan )
- Z04 - Quantitative visualization and analysis of synaptic proteins using nanobodies (Project Head Opazo, Felipe )
Completed projects
- A10 - Protein–protein interactions at the synapse monitored by quantitative protein cross-linking (Project Head Urlaub, Henning )
- B01 - The organization of structural lipids in synaptic membranes (Project Head Phan, Thi Ngoc Nhu )
- B03 - Mapping the protein and lipid organization in the plasma membrane of neurons using rapid rupture event imaging (Project Head Janshoff, Andreas )
- B09 - Cytoskeletal alterations contributing to synapto-axonal dysfunction in Parkinson’s disease (Project Head Lingor, Paul )
- Z03 - Simple multi-color super-resolution imaging by 10x expansion microscopy (Project Head Rizzoli, Ph.D., Silvio-Olivier )
Applicant Institution
Georg-August-Universität Göttingen
Participating Institution
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)
im Forschungsverbund Berlin e.V.; Max-Planck-Institut für Dynamik und Selbstorganisation (MPIDS); Max-Planck-Institut für biophysikalische Chemie
(Karl-Friedrich-Bonhoeffer-Institut) (aufgelöst); Max-Planck-Institut für experimentelle Medizin (aufgelöst); Max-Planck-Institut für medizinische Forschung; Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
c/o Charité - Universitätsmedizin Berlin; Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Standort Göttingen; Universitätsklinikum Hamburg-Eppendorf
im Forschungsverbund Berlin e.V.; Max-Planck-Institut für Dynamik und Selbstorganisation (MPIDS); Max-Planck-Institut für biophysikalische Chemie
(Karl-Friedrich-Bonhoeffer-Institut) (aufgelöst); Max-Planck-Institut für experimentelle Medizin (aufgelöst); Max-Planck-Institut für medizinische Forschung; Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
c/o Charité - Universitätsmedizin Berlin; Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Standort Göttingen; Universitätsklinikum Hamburg-Eppendorf
Spokesperson
Professor Silvio-Olivier Rizzoli, Ph.D.