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An alternative pathway for membrane protein biogenesis at the endoplasmic reticulum

Authors: O'Keefe, Sarah; Zong, Guanghui; Duah, Kwabena B; Andrews, Lauren E; Shi, Wei Q; High, Stephen;

An alternative pathway for membrane protein biogenesis at the endoplasmic reticulum

Abstract

AbstractThe heterotrimeric Sec61 complex is a major site for the biogenesis of transmembrane proteins (TMPs), accepting nascent TMP precursors that are targeted to the endoplasmic reticulum (ER) by the signal recognition particle (SRP). Unlike most single-spanning membrane proteins, the integration of type III TMPs is completely resistant to small molecule inhibitors of the Sec61 translocon. Using siRNA-mediated depletion of specific ER components, in combination with the potent Sec61 inhibitor ipomoeassin F (Ipom-F), we show that type III TMPs utilise a distinct pathway for membrane integration at the ER. Hence, following SRP-mediated delivery to the ER, type III TMPs can uniquely access the membrane insertase activity of the ER membrane complex (EMC) via a mechanism that is facilitated by the Sec61 translocon. This alternative EMC-mediated insertion pathway allows type III TMPs to bypass the Ipom-F-mediated blockade of membrane integration that is seen with obligate Sec61 clients.

Keywords

/82/29, 570, QH301-705.5, Immunoblotting, /13/106, /13, Endoplasmic Reticulum, Models, Biological, Article, /13/1, Animals, Humans, /631/45/612/1237, Biology (General), /13/89, /82, Membrane Proteins, Intracellular Membranes, Protein Transport, Protein Biosynthesis, /631/80/642/1463, RNA Interference, /82/1, Glycoconjugates, Signal Recognition Particle, SEC Translocation Channels, HeLa Cells

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
48
Top 1%
Top 10%
Top 1%
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