Shen Jingshi, Tareste David C, Paumet Fabienne, Rothman James E, Melia Thomas J
Department of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA.
Cell. 2007 Jan 12;128(1):183-95. doi: 10.1016/j.cell.2006.12.016.
Sec1/Munc18 (SM) proteins are required for every step of intracellular membrane fusion, but their molecular mechanism of action has been unclear. In this work, we demonstrate a fundamental role of the SM protein: to act as a stimulatory subunit of its cognate SNARE fusion machinery. In a reconstituted system, mammalian SNARE pairs assemble between bilayers to drive a basal fusion reaction. Munc18-1/nSec1, a synaptic SM protein required for neurotransmitter release, strongly accelerates this reaction through direct contact with both t- and v-SNAREs. Munc18-1 accelerates fusion only for the cognate SNAREs for exocytosis, therefore enhancing fusion specificity.
Sec1/Munc18(SM)蛋白是细胞内膜融合每个步骤所必需的,但它们的分子作用机制尚不清楚。在这项研究中,我们证明了SM蛋白的一个基本作用:作为其同源SNARE融合机制的刺激亚基。在一个重构系统中,哺乳动物SNARE对在双层膜之间组装以驱动基础融合反应。Munc18-1/nSec1是神经递质释放所需的一种突触SM蛋白,它通过与t-SNARE和v-SNARE直接接触,强烈加速这一反应。Munc18-1仅对同源的用于胞吐作用的SNAREs加速融合,从而提高融合特异性。