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结合蛋白/可溶性N-乙基马来酰胺敏感因子附着蛋白受体复合物的三维结构。

Three-dimensional structure of the complexin/SNARE complex.

作者信息

Chen Xiaocheng, Tomchick Diana R, Kovrigin Evguenii, Araç Demet, Machius Mischa, Südhof Thomas C, Rizo Josep

机构信息

Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

Neuron. 2002 Jan 31;33(3):397-409. doi: 10.1016/s0896-6273(02)00583-4.

Abstract

During neurotransmitter release, the neuronal SNARE proteins synaptobrevin/VAMP, syntaxin, and SNAP-25 form a four-helix bundle, the SNARE complex, that pulls the synaptic vesicle and plasma membranes together possibly causing membrane fusion. Complexin binds tightly to the SNARE complex and is essential for efficient Ca(2+)-evoked neurotransmitter release. A combined X-ray and TROSY-based NMR study now reveals the atomic structure of the complexin/SNARE complex. Complexin binds in an antiparallel alpha-helical conformation to the groove between the synaptobrevin and syntaxin helices. This interaction stabilizes the interface between these two helices, which bears the repulsive forces between the apposed membranes. These results suggest that complexin stabilizes the fully assembled SNARE complex as a key step that enables the exquisitely high speed of Ca(2+)-evoked neurotransmitter release.

摘要

在神经递质释放过程中,神经元SNARE蛋白突触囊泡蛋白/囊泡相关膜蛋白(synaptobrevin/VAMP)、 syntaxin和SNAP-25形成一个四螺旋束,即SNARE复合体,它将突触囊泡和质膜拉到一起,可能导致膜融合。结合蛋白紧密结合到SNARE复合体上,对于高效的Ca(2+)诱发的神经递质释放至关重要。一项结合X射线和基于TROSY的核磁共振研究现在揭示了结合蛋白/SNARE复合体的原子结构。结合蛋白以反平行α螺旋构象结合到突触囊泡蛋白和syntaxin螺旋之间的凹槽中。这种相互作用稳定了这两个螺旋之间的界面,该界面承受着相邻膜之间的排斥力。这些结果表明,结合蛋白稳定完全组装好的SNARE复合体是实现Ca(2+)诱发的神经递质释放极高速度的关键步骤。

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