Role of MICOS-dependent cristae membrane dynamics within mitochondria (B12)

• Subject Area: Biochemistry
• Term: since 2020
• Project identifier: Deutsche Forschungsgemeinschaft (DFG) - Project number 267205415

The ultrastructure of the cristae membrane is highly variable and strongly altered in numerous human dis-orders. Remodelling of this membrane is known for more than 50 years (condensed vs. orthodox state) and was shown to occur also during apoptosis. The MICOS ('Mitochondrial Contact Site and Cristae Organizing System') complex is a large membrane protein complex ensuring proper cristae membrane architecture. By using live-cell stimulated emission depletion (STED) nanoscopy we could show that cristae membranes are highly dynamic and are reorganising themselves at a time scale of seconds in a MICOS-dependent manner. In this project, we aim to get a molecular understanding of the mechanisms and the physiological function of cristae membrane dynamics in mammalian cells. To achieve these aims we will apply nanoscopic techniques in living mammalian cells in combination with biochemical and genetic methods.

• DFG Programme: Collaborative Research Centres
• Subproject of: SFB 1208: Identity and Dynamics of Membrane Systems - from Molecules to Cellular Functions
• Applicant Institution: Heinrich-Heine-Universität Düsseldorf
• Project Head: Professor Dr. Andreas Reichert