Chen Yong, Xu Yibin, Zhang Fan, Shin Yeon-Kyun
Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA.
EMBO J. 2004 Feb 25;23(4):681-9. doi: 10.1038/sj.emboj.7600083. Epub 2004 Feb 5.
SNARE complex formation is essential for intracellular membrane fusion. Vesicle-associated (v-) SNARE intertwines with target membrane (t-) SNARE to form a coiled coil that bridges two membranes and facilitates fusion. For the SNARE family involved in neuronal communications, complex formation is tightly regulated by the v-SNARE-membrane interactions. However, it was found using EPR that complex formation is spontaneous for a different SNARE family that is involved in protein trafficking in yeast. Further, reconstituted yeast SNAREs promoted membrane fusion, different from the inhibited fusion for reconstituted neuronal SNAREs. The EPR structural analysis showed that none of the coiled-coil residues of yeast v-SNARE is buried in the hydrophobic layer of the membrane, making the entire coiled-coil motif accessible, again different from the deep insertion of the membrane-proximal region of neuronal v-SNARE into the bilayer. Importantly, yeast membrane fusion is constitutively active, while synaptic membrane fusion is regulated, consistent with the present results for two SNARE families. Thus, the v-SNARE-membrane interaction may be a major molecular determinant for regulated versus constitutive membrane fusion in cells.
SNARE复合体的形成对于细胞内膜融合至关重要。囊泡相关(v-)SNARE与靶膜(t-)SNARE相互缠绕形成卷曲螺旋,该卷曲螺旋连接两个膜并促进融合。对于参与神经元通讯的SNARE家族,复合体的形成受到v-SNARE与膜相互作用的严格调控。然而,通过电子顺磁共振(EPR)发现,对于参与酵母中蛋白质运输的另一个SNARE家族,复合体的形成是自发的。此外,重组的酵母SNARE促进膜融合,这与重组的神经元SNARE抑制融合不同。EPR结构分析表明,酵母v-SNARE的卷曲螺旋残基均未埋入膜的疏水层中,使得整个卷曲螺旋基序可及,这再次与神经元v-SNARE的膜近端区域深深插入双层膜不同。重要的是,酵母膜融合是组成性激活的,而突触膜融合是受调控的,这与目前关于两个SNARE家族的结果一致。因此,v-SNARE与膜的相互作用可能是细胞中受调控的与组成性膜融合的主要分子决定因素。