4.5 Review Book Chapter

Conflicting Views on the Membrane Fusion Machinery and the Fusion Pore

Journal

ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY
Volume 25, Issue -, Pages 513-537

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.cellbio.24.110707.175239

Keywords

soluble NSF attachment protein receptor complex; exocytosis; synaptic vesicle; neurotransmitter release; synaptotagmin

Funding

  1. Deutsche Forschungsgerneinschaft [SFB-B16, GRK521]
  2. The Lundbeck Foundation
  3. Danish Medical Research Council
  4. Lundbeck Foundation [R28-2008-1976] Funding Source: researchfish

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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.

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