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A snapshot of membrane protein insertion
Author(s) -
Tanaka Yoshiki,
Tsukazaki Tomoya
Publication year - 2019
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.15252/embr.201949034
Subject(s) - snapshot (computer storage) , membrane protein , computational biology , biology , microbiology and biotechnology , membrane , computer science , genetics , operating system
The cytoplasm is the main place for protein translation from where nascent proteins are transported to their working areas, including the inside, outside, and membrane of the cell. The majority of newly synthesized membrane proteins is co‐translationally inserted into the membrane by the evolutionary conserved Sec translocon. In this issue of EMBO Reports , Kater et al [1] use single‐particle cryo‐electron microscopy to visualize a high‐resolution structure of the E. coli Sec YEG translocon:ribosome‐nascent chain complex in a lipid environment constituted by nanodiscs. This snapshot represents an early intermediate state in membrane protein insertion and provides important information for understanding the molecular mechanism of membrane protein biogenesis.