Fasshauer Dirk, Antonin Wolfram, Subramaniam Vinod, Jahn Reinhard
Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, AM Fassberg 11, 37077 Göttingen, Germany.
Nat Struct Biol. 2002 Feb;9(2):144-51. doi: 10.1038/nsb750.
SNARE proteins are essential for intracellular membrane fusion of eukaryotes. Their assembly into stable four-helix bundles bridges membranes and may provide the energy for initiating membrane fusion. In vitro, assembly of soluble SNARE fragments is accompanied by major structural rearrangements that can be described as a folding reaction. The pathways and the thermodynamics of SNARE protein interactions, however, are not known. Here we report that assembly and dissociation of two distantly related SNARE complexes exhibit a marked hysteresis. The assembled and disassembled native states are separated by a kinetic barrier and cannot equilibrate on biologically relevant timescales. We suggest that the hysteresis is a hallmark of all SNARE complexes and that complex assembly and disassembly follow different pathways that may be independently controlled.
SNARE蛋白对于真核生物细胞内膜融合至关重要。它们组装成稳定的四螺旋束连接膜,并可能为启动膜融合提供能量。在体外,可溶性SNARE片段的组装伴随着主要的结构重排,这可被描述为一种折叠反应。然而,SNARE蛋白相互作用的途径和热力学尚不清楚。在此我们报告,两种远缘相关的SNARE复合物的组装和解离表现出明显的滞后现象。组装态和解离态的天然状态被一个动力学屏障分隔开,并且在生物学相关的时间尺度上无法达到平衡。我们认为,滞后现象是所有SNARE复合物的一个标志,并且复合物的组装和解离遵循不同的途径,这些途径可能是独立可控的。