A structural perspective on tail-anchored protein biogenesis by the GET pathway

被引:34
作者
Mateja, Agnieszka [1 ]
Keenan, Robert J. [1 ]
机构
[1] Univ Chicago, Dept Biochem & Mol Biol, 929 East 57th St, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
ENDOPLASMIC-RETICULUM MEMBRANE; CRYSTAL-STRUCTURE; TARGETING FACTOR; TERMINAL DOMAIN; INSERTION; COMPLEX; MECHANISM; GET3; IDENTIFICATION; RECOGNITION;
D O I
10.1016/j.sbi.2018.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many tail-anchored (TA) membrane proteins are targeted to and inserted into the endoplasmic reticulum (ER) by the 'guided entry of tail-anchored proteins' (GET) pathway. This post translational pathway uses transmembrane-domain selective cytosolic chaperones for targeting, and a dedicated membrane protein complex for insertion. The past decade has seen rapid progress towards defining the molecular basis of TA protein biogenesis by the GET pathway. Here we review the mechanisms underlying each step of the pathway, emphasizing recent structural work and highlighting key questions that await future studies.
引用
收藏
页码:195 / 202
页数:8
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