A clamping mechanism involved in SNARE-dependent exocytosis

被引:265
作者
Giraudo, Claudio G. [1 ]
Eng, William S. [1 ]
Melia, Thomas J. [1 ]
Rothman, James E. [1 ]
机构
[1] Columbia Univ, Dept Physiol & Cellular Biophys, New York, NY 10032 USA
关键词
D O I
10.1126/science.1129450
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
During neurotransmitter release at the synapse, influx of calcium ions stimulates the release of neurotransmitter. However, the mechanism by which synaptic vesicle fusion is coupled to calcium has been unclear, despite the identification of both the core fusion machinery [soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE)] and the principal calcium sensor (synaptotagmin). Here, we describe what may represent a basic principle of the coupling mechanism: a reversible clamping protein (complexin) that can freeze the SNAREpin, an assembled fusion-competent intermediate en route to fusion. When calcium binds to the calcium sensor synaptotagmin, the clamp would then be released. SNARE proteins, and key regulators like synaptotagmin and complexin, can be ectopically expressed on the cell surface. Celts expressing such "flipped" synaptic SNARES fuse constitutively, but when we coexpressed complexin, fusion was blocked. Adding back calcium triggered fusion from this intermediate in the presence of synaptotagmin.
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页码:676 / 680
页数:5
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