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一种参与依赖SNARE的胞吐作用的钳夹机制。

A clamping mechanism involved in SNARE-dependent exocytosis.

作者信息

Giraudo Claudio G, Eng William S, Melia Thomas J, Rothman James E

机构信息

Department of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA.

出版信息

Science. 2006 Aug 4;313(5787):676-80. doi: 10.1126/science.1129450. Epub 2006 Jun 22.

Abstract

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. Cells 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.

摘要

在突触处神经递质释放过程中,钙离子内流刺激神经递质释放。然而,尽管已经鉴定出核心融合机制[可溶性N - 乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)]和主要钙传感器(突触结合蛋白),但突触小泡融合与钙偶联的机制仍不清楚。在这里,我们描述了可能代表偶联机制基本原理的内容:一种可逆钳制蛋白(复合体),它可以使SNAREpin(一种在融合途中组装好的具有融合能力的中间体)冻结。当钙与钙传感器突触结合蛋白结合时,钳制就会被释放。SNARE蛋白以及像突触结合蛋白和复合体这样的关键调节因子可以在细胞表面异位表达。表达这种“翻转”的突触SNARE的细胞会持续融合,但当我们共表达复合体时,融合被阻断。在存在突触结合蛋白的情况下,加入钙会触发从这个中间体开始的融合。

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