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PMID: 3961485 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Uncoupling translocation from translation: implications for transport of proteins across membranes.

Science (New York, N.Y.) ·Vol. 232 ·No. 4748 ·1986-04-18 ·Pages 348-52

Perara E, Rothman RE, Lingappa VR

Abstract

The segregation of secretory proteins into the cisternae of the endoplasmic reticulum (ER) is normally tightly coupled to their synthesis. This feature distinguishes their biogenesis from that of proteins targeted to many other organelles. In the examples presented, translocation across the ER membrane is dissociated from translation. Transport, which is normally cotranslational, may proceed in the absence of chain elongation. Moreover, translocation across the ER membrane does not proceed spontaneously since, even in the absence of protein synthesis, energy substrates are required for translocation. These conclusions have been extended to the cotranslational integration of newly synthesized transmembrane proteins.

MeSH Terms
Biological Transport Cell-Free System Electrophoresis, Polyacrylamide Gel Endoplasmic Reticulum/metabolism,physiology Intracellular Membranes/metabolism,physiology Microsomes/metabolism Protein Biosynthesis Proteins/metabolism RNA, Messenger/metabolism
Chemicals
Proteins RNA, Messenger
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Perara E
Rothman R E
Lingappa V R
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1986-04-18
Pages
348-52
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM31626 · United States
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