Data versus Dogma: New Challenges for SNARE-based Models of “Fast” Exocytosis at Nerve Terminals

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Cameron Gundersen

Abstract

Over the last several years, progress in understanding the molecular mechanism of fast, Ca2+-dependent exocytosis at nerve terminals has led to the following textbook picture:

The depolarization-dependent opening of presynaptic Ca2+ channels leads to a transient elevation of cytosolic Ca ion activity within the vicinity of docked synaptic vesicles. The binding of Ca2+ to synaptotagmin 1 (or, 2) then initiates a poorly understood reaction that allows vesicular and target SNAREs (soluble,N-ethylmaleimide-sensitivefactorattachment protein receptors) to complete their intermolecular coiling. The energy released by SNARE coiling then drives fusion between the membrane of suitably primed vesicles and the plasma membrane. Although there is widespread agreement that SNAREs and synaptotagmin are crucial for the molecular events that culminate in fast, synchronous exocytosis at neuronal synapses, there remains no consensus about how these proteins trigger the membrane fusion event that is central to this process. This review extends earlier criticisms of models implicating SNAREs in the terminal steps of the exocytotic cascade and explains how recent data are more compatible with a direct role for synaptotagmin 1 (or, 2) in this process.

 

 

 

Article Details

How to Cite
GUNDERSEN, Cameron. Data versus Dogma: New Challenges for SNARE-based Models of “Fast” Exocytosis at Nerve Terminals. International Biology Review, [S.l.], v. 1, n. 4, nov. 2016. ISSN 2572-7168. Available at: <http://journals.ke-i.org/index.php/ibr/article/view/789>. Date accessed: 13 dec. 2017. doi: https://doi.org/10.18103/ibr.v1i4.789.
Keywords
Key Words: synaptotagmin, syntaxin, synaptobrevin, SNAP-25, membrane fusion, electron tomography
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