Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Cold Spring Harb Perspect Biol. 2023 Mar 1;15(3):a041252. doi: 10.1101/cshperspect.a041252.
Tail-anchored (TA) proteins are an essential class of integral membrane proteins required for many aspects of cellular physiology. TA proteins contain a single carboxy-terminal transmembrane domain that must be post-translationally recognized, guided to, and ultimately inserted into the correct cellular compartment. The majority of TA proteins begin their biogenesis in the endoplasmic reticulum (ER) and utilize two parallel strategies for targeting and insertion: the guided-entry of tail-anchored proteins (GET) and ER-membrane protein complex (EMC) pathways. Here we focus on how these two sets of machinery target, transfer, and insert TAs into the lipid bilayer in close collaboration with quality control machinery. Additionally, we highlight the unifying features of the insertion process as revealed by recent structures of the GET and EMC membrane protein complexes.
尾部锚定(TA)蛋白是一类必需的跨膜蛋白,对于细胞生理学的许多方面都很重要。TA 蛋白含有单个羧基末端跨膜结构域,该结构域必须在翻译后被识别、导向并最终插入到正确的细胞隔室中。大多数 TA 蛋白在粗面内质网(ER)中开始其生物发生,并利用两种平行的靶向和插入策略:尾部锚定蛋白的引导进入(GET)和内质网-膜蛋白复合物(EMC)途径。在这里,我们重点关注这两套机制如何在质量控制机制的密切协作下,靶向、传递和将 TA 插入脂质双层。此外,我们还强调了最近 GET 和 EMC 膜蛋白复合物结构揭示的插入过程的统一特征。