AI Article Synopsis

  • Membrane tubulation coupled with fission (MTCF) is a common process, but understanding how it's coordinated is challenging due to the lack of proper monitoring techniques.
  • Using specially designed polymer cushioned bilayer islands, researchers investigated the interaction between the membrane tubulator BIN1 and the fission protein Dyn2.
  • Findings suggest that high ratios of Dyn2 to BIN1 lead to effective MTCF, as BIN1 helps recruit but restricts Dyn2 from binding to the membrane, linking this process to certain muscle diseases caused by mutations in these proteins.

Article Abstract

Membrane tubulation coupled with fission (MTCF) is a widespread phenomenon but mechanisms for their coordination remain unclear, partly because of the lack of assays to monitor dynamics of membrane tubulation and subsequent fission. Using polymer cushioned bilayer islands, we analyze the membrane tubulator Bridging Integrator 1 (BIN1) mixed with the fission catalyst dynamin2 (Dyn2). Our results reveal this mixture to constitute a minimal two-component module that demonstrates MTCF. MTCF is an emergent property and arises because BIN1 facilitates recruitment but inhibits membrane binding of Dyn2 in a dose-dependent manner. MTCF is therefore apparent only at high Dyn2 to BIN1 ratios. Because of their mutual involvement in T-tubules biogenesis, mutations in BIN1 and Dyn2 are associated with centronuclear myopathies and our analysis links the pathology with aberrant MTCF. Together, our results establish cushioned bilayer islands as a facile template for the analysis of membrane tubulation and inform of mechanisms that coordinate MTCF.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11098101PMC
http://dx.doi.org/10.1073/pnas.2402180121DOI Listing

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