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蛋白质翻译后跨内质网膜转运

Posttranslational protein translocation across the membrane of the endoplasmic reticulum.

作者信息

Rapoport T A, Matlack K E, Plath K, Misselwitz B, Staeck O

机构信息

Howard Hughes Medical Institute and Department of Cell Biology, Harvard Medical School, Boston, MA 02115-6091, USA.

出版信息

Biol Chem. 1999 Oct;380(10):1143-50. doi: 10.1515/BC.1999.145.

Abstract

Posttranslational protein translocation across the membrane of the endoplasmic reticulum is mediated by the Sec complex. This complex includes a transmembrane channel formed by multiple copies of the Sec61 protein. Translocation of a polypeptide begins when the signal sequence binds at a specific site within the channel. Binding results in the insertion of the substrate into the channel, possibly as a loop with a small segment exposed to the lumen. While bound, the signal sequence is in contact with both protein components of the channel and the lipid of the membrane. Subsequent movement of the polypeptide through the channel occurs when BiP molecules interact transiently with a luminal domain of the Sec complex, hydrolyze ATP, and bind to the substrate. Bound BiP promotes translocation by preventing the substrate from diffusing backwards through the channel, and thus acts as a molecular ratchet.

摘要

翻译后蛋白质跨内质网膜的转运由Sec复合体介导。该复合体包括由多个Sec61蛋白拷贝形成的跨膜通道。当信号序列在通道内的特定位点结合时,多肽的转运开始。结合导致底物插入通道,可能以一个小片段暴露于腔内的环的形式。结合时,信号序列与通道的蛋白质成分和膜脂都接触。当BiP分子与Sec复合体的腔内结构域短暂相互作用、水解ATP并与底物结合时,多肽随后通过通道移动。结合的BiP通过防止底物通过通道向后扩散来促进转运,因此起到分子棘轮的作用。

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