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TRAPPI tethers COPII vesicles by binding the coat subunit Sec23

机译:TRAPPI通过结合外壳亚基Sec23束缚COPII囊泡

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The budding of endoplasmic reticulum (ER)-derived vesicles is dependent on the COPII coat complex. Coat assembly is initiated when Sarl-GTP recruits the cargo adaptor complex, Sec23/Sec24, by binding to its GTPase-activating protein (GAP) Sec23 (ref. 2). This leads to the capture of transmembrane cargo by Sec24 (refs 3, 4) before the coat is polymerized by the Sec13/Sec31 complex. The initial interaction of a vesicle with its target membrane is mediated by tethers. We report here that in yeast and mammalian cells the tethering complex TRAPPI (ref. 7) binds to the coat subunit Sec23. This event requires the Bet3 subunit. In vitro studies demonstrate that the interaction between Sec23 and Bet3 targets TRAPPI to COPII vesicles to mediate vesicle tethering. We propose that the binding of TRAPPI to Sec23 marks a coated vesicle for fusion with another COPII vesicle or the Golgi apparatus. An implication of these findings is that the intracellular destination of a transport vesicle may be determined in part by its coat and its associated cargo.
机译:内质网(ER)衍生的囊泡的出芽取决于COPII外套复合物。当Sarl-GTP通过结合其GTPase激活蛋白(GAP)Sec23募集货物衔接子复合物Sec23 / Sec24时,即开始进行外套组装(参考文献2)。这导致在Sec13 / Sec31络合物聚合涂层之前,Sec24(参考文献3、4)捕获了跨膜货物。囊泡与其靶膜的初始相互作用是由系链介导的。我们在此报告,在酵母和哺乳动物细胞中,束缚复合物TRAPPI(参考文献7)与外壳亚基Sec23结合。此事件需要Bet3子单元。体外研究表明,Sec23和Bet3之间的相互作用将TRAPPI靶向COPII囊泡以介导囊泡束缚。我们建议将TRAPPI与Sec23的结合标记一个包被的囊泡,以便与另一个COPII囊泡或高尔基体融合。这些发现的暗示是,运输囊泡的细胞内目的地可能部分地取决于其囊泡及其相关货物。

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