Guiding tail-anchored membrane proteins to the endoplasmic reticulum in a chaperone cascade.

ABSTRACT: Newly synthesized integral membrane proteins must traverse the aqueous cytosolic environment before arrival at their membrane destination and are prone to aggregation, misfolding, and mislocalization during this process. The biogenesis of integral membrane proteins therefore poses acute challenges to protein homeostasis within a cell and requires the action of effective molecular chaperones. Chaperones that mediate membrane protein targeting not only need to protect the nascent transmembrane domains from improper exposure in the cytosol, but also need to accurately select client proteins and actively guide their clients to the appropriate target membrane. The mechanisms by which cellular chaperones work together to coordinate this complex process are only beginning to be delineated. Here,

SUBMITTER: Shan SO 

PROVIDER: S-EPMC6851334 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature