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N- to C-terminal SNARE complex assembly promotes rapid membrane fusion.

机译:从N端到C端的SNARE复合体可促进膜的快速融合。

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Assembly of the soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) syntaxin 1, SNAP-25, and synaptobrevin 2 is thought to be the driving force for the exocytosis of synaptic vesicles. However, whereas exocytosis is triggered at a millisecond time scale, the SNARE-mediated fusion of liposomes requires hours for completion, which challenges the idea of a key role for SNAREs in the final steps of exocytosis. We found that liposome fusion was dramatically accelerated when a stabilized syntaxin/SNAP-25 acceptor complex was used. Thus, SNAREs do have the capacity to execute fusion at a speed required for neuronal secretion, demonstrating that the maintenance of acceptor complexes is a critical step in biological fusion reactions.
机译:可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNAREs)语法1,SNAP-25和突触短纤维蛋白2的组装被认为是突触小泡胞吐的驱动力。然而,尽管胞吐作用是在毫秒级触发的,但是SNARE介导的脂质体融合需要数小时才能完成,这挑战了SNARE在胞吐作用的最终步骤中起关键作用的想法。我们发现当使用稳定的syntaxin / SNAP-25受体复合物时,脂质体融合得到了显着加速。因此,SNARE确实具有以神经元分泌所需的速度进行融合的能力,这表明维持受体复合物是生物融合反应中的关键步骤。

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