Project Details
SFB 1638: Cellular membrane remodelling – how changing form creates function
Subject Area
Biology
Term
since 2024
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 511488495
Membranes are fundamental for the generation of complex cellular architectures, as shown in the compartmentalization of eukaryotic cells. Biological membranes are highly dynamic structures with an adaptable composition of lipids and proteins, and membrane remodelling, the process of changing the composition or configuration of biological membranes, generates cell architecture and governs cell physiology. Every cellular membrane is subject to remodelling and the vast variety of different membrane configurations are tightly linked to a biological function. Not surprisingly, many different processes have been described, in which cells remodel their membranes. The molecular mechanisms, however, of most membrane remodelling processes are only partially understood or still entirely unknown. The overarching general principles of membrane remodelling are yet to be established and a comprehensive framework of how cells use these common principles to generate specific functions is missing. With this CRC we will address this gap in our knowledge from a conceptual point of view. We propose that four fundamental types of membrane remodelling underlie the large biological diversity: transverse and lateral segregation, as well as morphological and topological transformation. A major focus of this CRC is to proof the hypothesis that cells couple the four basic types of membrane remodelling in a modular manner, and that this coupling yields directional sequences of remodelling events that generate specific biological functions. Specifically, our goals are to identify remodelling pathways and the components involved, elucidate the molecular mechanisms of cellular membrane remodelling events, establish how individual membrane remodelling events are coupled and understand how a series of coupled membrane remodelling events work cooperatively, leading to functional switches. To achieve these aims, we have assembled projects that examine a broad range of biological processes that crucially depend on membrane remodelling events and that take place at different cellular membranes. The investigated processes are currently understood at different levels. Our projects range from the identification of pathways and the defining of the molecular players involved in certain membrane-based processes to reaching an understanding of membrane remodelling events at atomic resolution. Our program will be guided by one common goal: to define the universal logic of the coupling of membrane remodelling events. In the long run, we will show that our understanding is robust enough to reconstitute many of the investigated processes with purified components. By re-building these pathways and manipulating them with newly developed tool compounds we will open new routes to influence biological processes under physiological and pathological conditions.
DFG Programme
Collaborative Research Centres
Current projects
- P01 - Systematic analysis of ER-shaping Reticulon and REEP proteins (Project Head Schlaitz, Anne-Lore )
- P02 - Mechanisms of Endoplasmic Reticulum morphogenesis (Project Head Schuck, Sebastian )
- P03 - Membrane remodelling driven by SARS-CoV-2 proteins (Project Heads Chlanda, Petr ; Schwarz, Ulrich )
- P04 - Structure-function analysis of lipid remodelling in tail-anchored protein insertion into the ER membrane (Project Head Sinning, Irmgard )
- P05 - Membrane fluidity and lipid droplet formation in the ER of renal proximal tubular cells (Project Head Simons, Matias )
- P06 - Nuclear membrane remodelling during pore complex insertion (Project Head Ellenberg, Jan )
- P07 - Fusion of the inner and outer nuclear membranes during nuclear pore complex assembly (Project Head Schiebel, Elmar )
- P08 - Membrane remodelling during mitochondrial lipid transfer (Project Head Meinecke, Michael )
- P09 - Membrane remodelling during the mitochondrial unfolded protein response (Project Head Vögtle, Friederike-Nora )
- P10 - Synaptic exocytosis: dynamic molecular arrangements and intermediates on the path to lipid bilayer merger (Project Head Söllner, Thomas )
- P11 - Molecular mechanism driving disulfide formation during FGF2 oligomerization and membrane translocation (Project Heads Dick, Tobias ; Nickel, Walter )
- P12 - Mechanical regulation of membrane curvature during endocytosis (Project Heads Cavalcanti-Adam, Elisabetta Ada ; Diz-Muñoz, Alba )
- P13 - Mechanical and chemical crosstalk between membranes and anchored mechano-kinases (Project Heads Gräter, Frauke ; Nickel, Walter )
- P14 - ESCRT-III-mediated membrane remodelling in Archaea and Eukarya (Project Head Moser von Filseck, Joachim )
- P15 - Remodelling lipid membranes with DNA/RNA nanotechnology (Project Head Göpfrich, Kerstin )
- Z01 - Molecular Dynamics Simulations of Membrane Systems (Project Heads Gräter, Frauke ; Lolicato, Fabio )
- Z02 - Spatial lipidomics and targeted lipid analytics (Project Heads Brügger, Britta ; Hopf, Carsten )
- Z03 - Cryo-EM and cryo-correlative approaches to study membrane remodelling (Project Heads Chlanda, Petr ; Paulino, Cristina )
- Z04 - Central Administration (Project Head Meinecke, Michael )
- ZINF - Information Infrastructure for SFB1638 (Project Heads Kopp, Jürgen ; Sinning, Irmgard )
Applicant Institution
Ruprecht-Karls-Universität Heidelberg
Participating University
Hochschule Mannheim
Participating Institution
Deutsches Krebsforschungszentrum (DKFZ); European Molecular Biology Laboratory (EMBL); Max-Planck-Institut für medizinische Forschung
Spokesperson
Professor Dr. Michael Meinecke