Farkas Ákos, Bohnsack Katherine E
Department of Molecular Biology, University Medical Center Göttingen, Göttingen, Germany.
J Cell Biol. 2021 Aug 2;220(8). doi: 10.1083/jcb.202105004. Epub 2021 Jul 15.
Tail-anchored (TA) proteins fulfill diverse cellular functions within different organellar membranes. Their characteristic C-terminal transmembrane segment renders TA proteins inherently prone to aggregation and necessitates their posttranslational targeting. The guided entry of TA proteins (GET in yeast)/transmembrane recognition complex (TRC in humans) pathway represents a major route for TA proteins to the endoplasmic reticulum (ER). Here, we review important new insights into the capture of nascent TA proteins at the ribosome by the GET pathway pretargeting complex and the mechanism of their delivery into the ER membrane by the GET receptor insertase. Interestingly, several alternative routes by which TA proteins can be targeted to the ER have emerged, raising intriguing questions about how selectivity is achieved during TA protein capture. Furthermore, mistargeting of TA proteins is a fundamental cellular problem, and we discuss the recently discovered quality control machineries in the ER and outer mitochondrial membrane for displacing mislocalized TA proteins.
尾锚定(TA)蛋白在不同的细胞器膜内发挥多种细胞功能。其特有的C末端跨膜片段使TA蛋白天生易于聚集,因此需要进行翻译后靶向运输。TA蛋白的引导进入(酵母中的GET)/跨膜识别复合物(人类中的TRC)途径是TA蛋白进入内质网(ER)的主要途径。在此,我们综述了关于GET途径预靶向复合物在核糖体上捕获新生TA蛋白以及GET受体插入酶将其递送至内质网膜的机制的重要新见解。有趣的是,已经出现了几种TA蛋白靶向内质网的替代途径,这引发了关于TA蛋白捕获过程中如何实现选择性的有趣问题。此外,TA蛋白的错误靶向是一个基本的细胞问题,我们讨论了内质网和线粒体外膜中最近发现的用于置换错误定位的TA蛋白的质量控制机制。