Abstract
The Sec61 complex is the proteinaceous pore through which one-third of mammalian polypeptides access the lumen of the endoplasmic reticulum (ER) during their translocation across, or insertion into, the ER membrane. N-terminal ER signal peptides mediate polypeptide targeting to, and opening of, the Sec61 channel in a substrate-specific manner. Here, we discuss the recently defined features of ER signal peptides which necessitate the use of the accessory components Sec62 and Sec63 during the Sec61-mediated cotranslational translocation of newly synthesized secretory proteins.
Original language | English |
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Journal | FEBS Journal |
Volume | 287 |
Issue number | 21 |
Pages (from-to) | 4607-4611 |
Number of pages | 5 |
ISSN | 1742-464X |
DOIs |
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Publication status | Published - 1 Nov 2020 |
Externally published | Yes |
MoE publication type | A1 Journal article-refereed |
Bibliographical note
Funding Information:The authors thank Lisa Swanton for advice. This work was supported by a Wellcome Trust Investigator Award in Science (204957/Z/16/Z).
Publisher Copyright:
© 2020 Federation of European Biochemical Societies
Fields of Science
- endoplasmic reticulum
- Sec61 complex
- Sec62/Sec63
- signal peptides
- translocon gating