Synaptotagmin oligomers are necessary and can be sufficient to form a Ca2+ -sensitive fusion clamp

FEBS Lett. 2019 Jan;593(2):154-162. doi: 10.1002/1873-3468.13317. Epub 2019 Jan 18.

Abstract

The buttressed-ring hypothesis, supported by recent cryo-electron tomography analysis of docked synaptic-like vesicles in neuroendocrine cells, postulates that prefusion SNAREpins are stabilized and organized by Synaptotagmin (Syt) ring-like oligomers. Here, we use a reconstituted single-vesicle fusion analysis to test the prediction that destabilizing the Syt1 oligomers destabilizes the clamp and results in spontaneous fusion in the absence of Ca2+ . Vesicles in which Syt oligomerization is compromised by a ring-destabilizing mutation dock and diffuse freely on the bilayer until they fuse spontaneously, similar to vesicles containing only v-SNAREs. In contrast, vesicles containing wild-type Syt are immobile as soon as they attach to the bilayer and remain frozen in place, up to at least 1 h until fusion is triggered by Ca2+ .

Keywords: SNARE proteins; Synaptotagmin; calcium; fusion clamp; single-vesicle analysis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Cryoelectron Microscopy
  • Electron Microscope Tomography
  • Membrane Fusion
  • Mutation
  • Protein Multimerization
  • SNARE Proteins / genetics
  • SNARE Proteins / metabolism*
  • Synaptic Vesicles / metabolism*
  • Synaptotagmin I / chemistry*
  • Synaptotagmin I / genetics
  • Synaptotagmin I / metabolism*

Substances

  • SNARE Proteins
  • Synaptotagmin I
  • Calcium