Hu Kuang, Carroll Joe, Rickman Colin, Davletov Bazbek
MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, United Kingdom.
J Biol Chem. 2002 Nov 1;277(44):41652-6. doi: 10.1074/jbc.M205044200. Epub 2002 Aug 27.
Calcium-dependent synaptic vesicle exocytosis requires three SNARE (soluble N-ethylmaleimide-sensitive-factor attachment protein receptor) proteins: synaptobrevin/vesicle-associated membrane protein in the vesicular membrane and syntaxin and SNAP-25 in the presynaptic membrane. The SNAREs form a thermodynamically stable complex that is believed to drive fusion of vesicular and presynaptic membranes. Complexin, also known as synaphin, is a neuronal cytosolic protein that acts as a positive regulator of synaptic vesicle exocytosis. Complexin binds selectively to the neuronal SNARE complex, but how this promotes exocytosis remains unknown. Here we used purified full-length and truncated SNARE proteins and a gel shift assay to show that the action of complexin on SNARE complex depends strictly on the transmembrane regions of syntaxin and synaptobrevin. By means of a preparative immunoaffinity procedure to achieve total extraction of SNARE complex from brain, we demonstrated that complexin is the only neuronal protein that tightly associates with it. Our data indicated that, in the presence of complexin, the neuronal SNARE proteins assemble directly into a complex in which the transmembrane regions interact. We propose that complexin facilitates neuronal exocytosis by promoting interaction between the complementary syntaxin and synaptobrevin transmembrane regions that reside in opposing membranes prior to fusion.
钙依赖性突触小泡胞吐作用需要三种SNARE(可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体)蛋白:突触小泡膜中的突触小泡蛋白/囊泡相关膜蛋白以及突触前膜中的 syntaxin和SNAP-25。SNARE蛋白形成一种热力学稳定的复合物,据信该复合物驱动囊泡膜与突触前膜的融合。结合蛋白,也称为突触结合蛋白,是一种神经元胞质蛋白,作为突触小泡胞吐作用的正向调节剂。结合蛋白选择性地结合神经元SNARE复合物,但这如何促进胞吐作用仍不清楚。在这里,我们使用纯化的全长和截短的SNARE蛋白以及凝胶迁移试验来表明结合蛋白对SNARE复合物的作用严格依赖于syntaxin和突触小泡蛋白的跨膜区域。通过一种制备性免疫亲和程序从脑中实现SNARE复合物的完全提取,我们证明结合蛋白是唯一与之紧密结合的神经元蛋白。我们的数据表明,在结合蛋白存在的情况下,神经元SNARE蛋白直接组装成一个复合物,其中跨膜区域相互作用。我们提出,结合蛋白通过促进互补的syntaxin和突触小泡蛋白跨膜区域之间的相互作用来促进神经元胞吐作用,这些跨膜区域在融合前位于相对的膜中。