Rearrangements under confinement lead to increased binding energy of Synaptotagmin-1 with anionic membranes in Mg2+ and Ca2

FEBS Lett. 2018 May;592(9):1497-1506. doi: 10.1002/1873-3468.13040. Epub 2018 Apr 10.

Abstract

Synaptotagmin-1 (Syt1) is the primary calcium sensor (Ca2+ ) that mediates neurotransmitter release at the synapse. The tandem C2 domains (C2A and C2B) of Syt1 exhibit functionally critical, Ca2+ -dependent interactions with the plasma membrane. With the surface forces apparatus, we directly measure the binding energy of membrane-anchored Syt1 to an anionic membrane and find that Syt1 binds with ~6 kB T in EGTA, ~10 kB T in Mg2+ and ~18 kB T in Ca2+ . Molecular rearrangements measured during confinement are more prevalent in Ca2+ and Mg2+ and suggest that Syt1 initially binds through C2B, then reorients the C2 domains into the preferred binding configuration. These results provide energetic and mechanistic details of the Syt1 Ca2+ -activation process in synaptic transmission.

Keywords: membrane fusion; neurotransmission; synaptotagmin.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / pharmacology*
  • Cell Membrane / metabolism*
  • Dose-Response Relationship, Drug
  • Magnesium / pharmacology*
  • Protein Binding / drug effects
  • Surface Properties
  • Synaptotagmin I / metabolism*
  • Thermodynamics

Substances

  • Synaptotagmin I
  • Magnesium
  • Calcium