Journal
EMBO JOURNAL
Volume 31, Issue 15, Pages 3270-3281Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/emboj.2012.164
Keywords
exocytosis; fusion; reconstitution; SNARE; synaptic vesicle
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Funding
- German Research Foundation [SFB/TRR 83]
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Regulated exocytosis requires that the assembly of the basic membrane fusion machinery is temporarily arrested. Synchronized membrane fusion is then caused by a specific trigger-a local rise of the Ca2+ concentration. Using reconstituted giant unilamellar vesicles (GUVs), we have analysed the role of complexin and membrane-anchored synaptotagmin 1 in arresting and synchronizing fusion by lipid-mixing and cryo-electron microscopy. We find that they mediate the formation and consumption of docked small unilamellar vesicles (SUVs) via the following sequence of events: Synaptotagmin 1 mediates v-SNARE-SUV docking to t-SNARE-GUVs in a Ca2+-independent manner. Complexin blocks vesicle consumption, causing accumulation of docked vesicles. Together with synaptotagmin 1, complexin synchronizes and stimulates rapid fusion of accumulated docked vesicles in response to physiological Ca2+ concentrations. Thus, the reconstituted assay resolves both the stimulatory and inhibitory function of complexin and mimics key aspects of synaptic vesicle fusion. The EMBO Journal (2012) 31, 3270-3281. doi:10.1038/emboj.2012.164; Published online 15 June 2012
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