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A clamping mechanism involved in SNARE-dependent exocytosis.

机译:钳制机制参与SNARE依赖的胞吐作用。

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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.
机译:在突触释放神经递质的过程中,钙离子的涌入会刺激神经递质的释放。然而,尽管已经确定了核心融合机制[可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)]和主要的钙传感器(突触标签蛋白),但突触小泡融合至钙的机制仍不清楚。在这里,我们描述了可能代表偶联机理的基本原理:一种可逆的夹持蛋白(复合蛋白),可以使SNAREpin冻结,SNAREpin是一种组装好的具有融合能力的中间体,可以融合。当钙结合到钙传感器突触素上时,夹具将被释放。 SNARE蛋白和关键调节剂(如突触结合蛋白和复合蛋白)可以在细胞表面异位表达。表达这种“翻转的”突触SNARE的细胞组成性融合,但是当我们共表达复合蛋白时,融合被阻止。在突触结合蛋白存在下,从该中间体中添加回钙引发了融合。

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