| Literature DB >> 23178715 |
Qinghua Fang1, Ying Zhao, Manfred Lindau.
Abstract
Synaptobrevin 2 (Syb2), syntaxin (Sx1A), and SNAP-25, generate a force to induce fusion pore formation. The v-SNARE, Syb2, is anchored to the vesicle membrane by a single transmembrane domain. Here we show that 2 tryptophans (W89/W90) located in the juxtamembrane domain of Syb2, which stabilize the transmembrane (TM) domain position, control the ratio of spontaneous vs. stimulated membrane fusion events in chromaffin cells. Changing the 2 hydrophobic tryptophans to neutral alanines promotes spontaneous membrane fusion, faster transmitter release kinetics and complete release from individual vesicles. The results indicate that the two tryptophans act as a fusion clamp making fusion stimulus-dependent.Entities:
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Year: 2012 PMID: 23178715 PMCID: PMC3529983 DOI: 10.1016/j.febslet.2012.11.002
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124