v-SNARE transmembrane domains function as catalysts for vesicle fusion

Elife. 2016 Jun 25;5:e17571. doi: 10.7554/eLife.17571.

Abstract

Vesicle fusion is mediated by an assembly of SNARE proteins between opposing membranes, but it is unknown whether transmembrane domains (TMDs) of SNARE proteins serve mechanistic functions that go beyond passive anchoring of the force-generating SNAREpin to the fusing membranes. Here, we show that conformational flexibility of synaptobrevin-2 TMD is essential for efficient Ca(2+)-triggered exocytosis and actively promotes membrane fusion as well as fusion pore expansion. Specifically, the introduction of helix-stabilizing leucine residues within the TMD region spanning the vesicle's outer leaflet strongly impairs exocytosis and decelerates fusion pore dilation. In contrast, increasing the number of helix-destabilizing, ß-branched valine or isoleucine residues within the TMD restores normal secretion but accelerates fusion pore expansion beyond the rate found for the wildtype protein. These observations provide evidence that the synaptobrevin-2 TMD catalyzes the fusion process by its structural flexibility, actively setting the pace of fusion pore expansion.

Keywords: exocytosis; membrane fusion; mouse; neuroscience; neurotransmitter release; synaptobrevin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • DNA Mutational Analysis
  • Exocytosis*
  • Membrane Fusion*
  • Mice
  • Models, Biological
  • Mutant Proteins / chemistry
  • Mutant Proteins / genetics*
  • Mutant Proteins / metabolism*
  • Protein Conformation
  • Secretory Vesicles / metabolism*
  • Vesicle-Associated Membrane Protein 2 / chemistry
  • Vesicle-Associated Membrane Protein 2 / genetics*
  • Vesicle-Associated Membrane Protein 2 / metabolism*

Substances

  • Mutant Proteins
  • Vesicle-Associated Membrane Protein 2