Das Sunit, Gerwin Claudia, Sheng Zu-Hang
Synaptic Function Unit, NINDS, National Institutes of Health, Bethesda, Maryland 20892-4154, USA.
J Biol Chem. 2003 Oct 17;278(42):41221-6. doi: 10.1074/jbc.M304851200. Epub 2003 Aug 1.
Syntaphilin is a brain-specific syntaxin-binding partner first characterized as an inhibitor of SNARE complex formation and neurotransmitter release. Here we show that syntaphilin also binds to dynamin-1 and through this interaction inhibits dynamin-mediated endocytosis. Immunoprecipitation studies from cross-linked rat synaptosomes demonstrate that an endogenous syntaphilin-dynamin-1 complex exists independently of dynamin-1 binding to amphiphysin. Functionally, syntaphilin expression inhibits transferrin internalization in COS-7 cells. These data reveal that syntaphilin is an inhibitor of both SNARE-based fusion and dynamin-mediated endocytosis.
突触结合蛋白是一种大脑特异性的 syntaxin 结合蛋白,最初被鉴定为 SNARE 复合体形成和神经递质释放的抑制剂。在此我们表明,突触结合蛋白还与发动蛋白 -1 结合,并通过这种相互作用抑制发动蛋白介导的内吞作用。来自交联大鼠突触体的免疫沉淀研究表明,内源性突触结合蛋白 - 发动蛋白 -1 复合体独立于发动蛋白 -1 与 amphiphysin 的结合而存在。在功能上,突触结合蛋白的表达抑制了 COS-7 细胞中运铁蛋白的内化。这些数据表明,突触结合蛋白是基于 SNARE 的融合和发动蛋白介导的内吞作用的抑制剂。