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PMID: 19575641 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Conflicting views on the membrane fusion machinery and the fusion pore.

Annual review of cell and developmental biology ·Vol. 25 ·2009-00-00 ·Pages 513-37

Sørensen JB

Abstract

Fast exocytosis of synaptic vesicles differs from other membrane fusion reactions by being under tight temporal control by the intracellular calcium concentration. This is achieved by subjecting the SNARE-dependent fusion pathway to additional layers of control, both upstream and downstream of the assembly of the fusogenic SNARE-complex. Here, I review conflicting views on the function of the core fusion machinery consisting of the SNAREs, Munc18, complexin, and synaptotagmin. Munc18 controls docking of vesicles to the plasma membrane and initial SNARE-complex assembly, whereas complexin and synaptotagmin cooperate in holding the SNARE complex in an intermediate release-ready or cocked state. Different effects of complexin and synaptotagmin shape the energy landscape for fusion and make final fusion calcium triggered. The final steps are fusion pore formation and expansion, which allow release of the water-soluble vesicle content. The fusion pore remains the most elusive part of the exocytosis pathway, owing to its short lifetime.

MeSH Terms
Animals Calcium/metabolism Exocytosis Membrane Fusion Munc18 Proteins/metabolism SNARE Proteins/metabolism Synaptic Vesicles/metabolism Synaptotagmins/metabolism
Chemicals
Munc18 Proteins SNARE Proteins Synaptotagmins Calcium
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Sørensen Jakob B
Department of Neuroscience and Pharmacology, Faculty of Health Sciences, University of Copenhagen, 2200 Copenhagen N, Denmark. [email protected]
Article Info
Journal
Annual review of cell and developmental biology
Abbr.
Annu Rev Cell Dev Biol
ISSN
1530-8995
Published
2009-00-00
Pages
513-37
Language
English
Region
United States
NLM ID
9600627
Subset
IM
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