4.8 Article

Relaxation of Loaded ESCRT-III Spiral Springs Drives Membrane Deformation

Journal

CELL
Volume 163, Issue 4, Pages 866-879

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2015.10.017

Keywords

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Funding

  1. Human Frontier Science Program (HFSP)
  2. European Research Council (ERC) [RGY0076-2008, 310080-MEM-STRUCT-AFM]
  3. Swiss National Fund for Research [311536-MEMFIS]
  4. European Commission [300532-2011]
  5. Agence Nationale de la Recherche, France (ANR)
  6. ANR-Nano [ANR-12-BS10-009-01]
  7. ANR-BBMS [ANR-12-BSV8-0006-01]
  8. Universite Paris-Sud and CNRS
  9. Marie Curie Integration Grant [PCIG12-GA-2012-334053]
  10. Investissements d'Avenir'' LabEx PALM [ANR-10-LABX-0039-PALM]
  11. [131003A_130520]
  12. [131003A_149975]
  13. Agence Nationale de la Recherche (ANR) [ANR-12-BSV8-0006] Funding Source: Agence Nationale de la Recherche (ANR)

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ESCRT-III is required for lipid membrane remodeling in many cellular processes, from abscission to viral budding and multi-vesicular body biogenesis. However, how ESCRT-III polymerization generates membrane curvature remains debated. Here, we show that Snf7, the main component of ESCRT-III, polymerizes into spirals at the surface of lipid bilayers. When covering the entire membrane surface, these spirals stopped growing when densely packed: they had a polygonal shape, suggesting that lateral compression could deform them. We reasoned that Snf7 spirals could function as spiral springs. By measuring the polymerization energy and the rigidity of Snf7 filaments, we showed that they were deformed while growing in a confined area. Furthermore, we observed that the elastic expansion of compressed Snf7 spirals generated an area difference between the two sides of the membrane and thus curvature. This spring-like activity underlies the driving force by which ESCRT-III could mediate membrane deformation and fission.

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