Grusovin J, Stoichevska V, Gough K H, Nunan K, Ward C W, Macaulay S L
CSIRO Health Sciences and Nutrition, 343 Royal Parade, Parkville 3052, Victoria, Australia.
Biochem J. 2000 Sep 15;350 Pt 3(Pt 3):741-6.
munc18c is a critical protein involved in trafficking events associated with syntaxin 4 and which also mediates inhibitory effects on vesicle docking and/or fusion. To investigate the domains of munc18c responsible for its interaction with syntaxin 4, fragments of munc18c were generated and their interaction with syntaxin 4 examined in vivo by the yeast two-hybrid assay. In vitro protein-protein interaction studies were then used to confirm that the interaction between the proteins was direct. Full-length munc18c(1-592), munc18c(1-139) and munc18c(1-225), but not munc18c(226-592), munc18c(1-100), munc18c(43-139) or munc18c(66-139), interacted with the cytoplasmic portion of syntaxin 4, Stx4(2-273), as assessed by yeast two-hybrid assay of growth on nutritionally deficient media and by beta-galactosidase reporter induction. The N-terminal predicted helix-a-helix-b-helix-c region of syntaxin 4, Stx4(29-157), failed to interact with full-length munc18c(1-592), indicating that a larger portion of syntaxin 4 is necessary for the interaction. The yeast two-hybrid results were confirmed by protein-protein interaction studies between Stx4(2-273) and glutathione S-transferase fusion proteins of munc18c. Full-length munc18c(1-592), munc18c(1-139) and munc18c(1-225) interacted with Stx4(2-273) whereas munc18c(1-100) did not, consistent with the yeast two-hybrid data. These data thus identify a region of munc18c between residues 1 and 139 as a minimal domain for its interaction with syntaxin 4.
munc18c是一种关键蛋白,参与与Syntaxin 4相关的运输事件,并且还介导对囊泡对接和/或融合的抑制作用。为了研究munc18c中负责其与Syntaxin 4相互作用的结构域,生成了munc18c的片段,并通过酵母双杂交试验在体内检测它们与Syntaxin 4的相互作用。然后进行体外蛋白质-蛋白质相互作用研究,以确认蛋白质之间的相互作用是直接的。全长munc18c(1-592)、munc18c(1-139)和munc18c(1-225),而不是munc18c(226-592)、munc18c(1-100)、munc18c(43-139)或munc18c(66-139),与Syntaxin 4的胞质部分Stx4(2-273)相互作用,这是通过在营养缺陷培养基上生长的酵母双杂交试验和β-半乳糖苷酶报告基因诱导来评估的。Syntaxin 4的N端预测的螺旋-a-螺旋-b-螺旋-c区域Stx4(29-157)未能与全长munc18c(1-592)相互作用,表明Syntaxin 4的更大一部分对于这种相互作用是必需的。酵母双杂交结果通过Stx4(2-273)与munc18c的谷胱甘肽S-转移酶融合蛋白之间的蛋白质-蛋白质相互作用研究得到证实。全长munc18c(1-592)、munc18c(1-139)和munc18c(1-225)与Stx4(2-273)相互作用,而munc18c(1-100)则不与Stx4(2-273)相互作用,这与酵母双杂交数据一致。因此,这些数据确定了munc18c中1至139位残基之间的区域是其与Syntaxin 4相互作用的最小结构域。