Re-examining how Complexin Inhibits Neurotransmitter Release: SNARE complex Insertion or Electrostatic Hindrance?

被引:61
|
作者
Trimbuch, Thorsten [1 ]
Xu, Junjie [2 ]
Flaherty, David [2 ]
Tomchick, Diana R. [2 ]
Rizo, Josep [2 ,3 ,4 ]
Rosenmund, Christian [1 ]
机构
[1] Charite, Neurosci Res Ctr, NeuroCure Cluster Excellence, D-10117 Berlin, Germany
[2] Univ Texas SW Med Ctr Dallas, Dept Biophys, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
来源
ELIFE | 2014年 / 3卷
关键词
SYNAPTIC VESICLE EXOCYTOSIS; MEMBRANE-FUSION; CRYSTAL-STRUCTURE; BINDING; PROTEIN; SYNAPTOTAGMIN; INTERPLAY; SYNAPSES; DOCKING; SYSTEM;
D O I
10.7554/eLife.02391
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Complexins play activating and inhibitory functions in neurotransmitter release. The complexin accessory helix inhibits release and was proposed to insert into SNARE complexes to prevent their full assembly. This model was supported by 'superclamp' and 'poor-clamp' mutations that enhanced or decreased the complexin-I inhibitory activity in cell-cell fusion assays, and by the crystal structure of a superclamp mutant bound to a synaptobrevin-truncated SNARE complex. NMR studies now show that the complexin-I accessory helix does not insert into synaptobrevin-truncated SNARE complexes in solution, and electrophysiological data reveal that superclamp mutants have slightly stimulatory or no effects on neurotransmitter release, whereas a poor-clamp mutant inhibits release. Importantly, increasing or decreasing the negative charge of the complexin-I accessory helix inhibits or stimulates release, respectively. These results suggest a new model whereby the complexin accessory helix inhibits release through electrostatic (and perhaps steric) repulsion enabled by its location between the vesicle and plasma membranes.
引用
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页数:59
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