AI Article Synopsis

  • * Synaptotagmin proteins mainly handle synchronous release, while double C2 domain proteins (Doc2) serve as Ca2+ sensors for spontaneous release, showing higher Ca2+ sensitivity.
  • * Doc2 proteins compete with synaptotagmin-1 by binding to SNARE complexes, indicating a broader mechanism where different proteins regulate vesicle fusion based on their actions with SNAREs.

Article Abstract

Synaptic vesicle fusion in brain synapses occurs in phases that are either tightly coupled to action potentials (synchronous), immediately following action potentials (asynchronous), or as stochastic events in the absence of action potentials (spontaneous). Synaptotagmin-1, -2, and -9 are vesicle-associated Ca2+ sensors for synchronous release. Here we found that double C2 domain (Doc2) proteins act as Ca2+ sensors to trigger spontaneous release. Although Doc2 proteins are cytosolic, they function analogously to synaptotagmin-1 but with a higher Ca2+ sensitivity. Doc2 proteins bound to N-ethylmaleimide-sensitive factor attachment receptor (SNARE) complexes in competition with synaptotagmin-1. Thus, different classes of multiple C2 domain-containing molecules trigger synchronous versus spontaneous fusion, which suggests a general mechanism for synaptic vesicle fusion triggered by the combined actions of SNAREs and multiple C2 domain-containing proteins.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846320PMC
http://dx.doi.org/10.1126/science.1183765DOI Listing

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