Carr Chavela M, Munson Mary
Department of Pathology and Laboratory Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
EMBO Rep. 2007 Sep;8(9):834-8. doi: 10.1038/sj.embor.7401051.
Communication between neurons relies on chemical synapses and the release of neurotransmitters into the synaptic cleft. Neurotransmitter release is an exquisitely regulated membrane fusion event that requires the linking of an electrical nerve stimulus to Ca(2+) influx, which leads to the fusion of neurotransmitter-filled vesicles with the cell membrane. The timing of neurotransmitter release is controlled through the regulation of the soluble N-ethylmaleimide sensitive factor attachment receptor (SNARE) proteins-the core of the membrane fusion machinery. Assembly of the fusion-competent SNARE complex is regulated by several neuronal proteins, including complexin and the Ca(2+)-sensor synaptotagmin. Both complexin and synaptotagmin bind directly to SNAREs, but their mechanism of action has so far remained unclear. Recent studies revealed that synaptotagmin-Ca(2+) and complexin collaborate to regulate membrane fusion. These compelling new results provide a molecular mechanistic insight into the functions of both proteins: complexin 'clamps' the SNARE complex in a pre-fusion intermediate, which is then released by the action of Ca(2+)-bound synaptotagmin to trigger rapid fusion.
神经元之间的通讯依赖于化学突触以及神经递质释放到突触间隙。神经递质释放是一个受到精确调控的膜融合事件,它需要将电神经刺激与Ca(2+)内流相联系,进而导致充满神经递质的囊泡与细胞膜融合。神经递质释放的时机是通过对可溶性N-乙基马来酰亚胺敏感因子附着受体(SNARE)蛋白的调控来控制的,SNARE蛋白是膜融合机制的核心。具有融合能力的SNARE复合体的组装受到多种神经元蛋白的调控,包括复合体蛋白和Ca(2+)传感器突触结合蛋白。复合体蛋白和突触结合蛋白都直接与SNAREs结合,但其作用机制至今仍不清楚。最近的研究表明,突触结合蛋白-Ca(2+)和复合体蛋白协同调节膜融合。这些引人注目的新结果为这两种蛋白的功能提供了分子机制上的见解:复合体蛋白将SNARE复合体“钳制”在融合前的中间体中,然后通过与Ca(2+)结合的突触结合蛋白的作用将其释放,从而触发快速融合。