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The endoplasmic reticulum and unfolded protein response in the control of mammalian recombinant protein production

  • University of Manchester
Research Output:
Contribution to journal
Review article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Review article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 1581-1593 (13 pages)

Journal (Volume, Issue Number)

Biotechnology Letters (Volume 36, Issue 8)

Publication milestones

  • Published - 01/01/2014

Publication status

Published - 01/01/2014

ISSN

0141-5492

Publication IDs

  • Scopus: 84903714956
  • PubMed: 24752815

Abstract

The endoplasmic reticulum (ER) of eukaryotic cells is involved in the synthesis and processing of proteins and lipids in the secretory pathway. These processing events that proteins undergo in the ER may present major limiting steps for recombinant protein production. Increased protein synthesis, accumulation of improperly processed or mis-folded protein can induce ER stress. To cope with ER stress, the ER has quality control mechanisms, such as the unfolded protein response (UPR) and ER-associated degradation to restore homeostasis. ER stress and UPR activation trigger multiple physiological cellular changes. Here we review cellular mechanisms that cope with ER stress and illustrate how this knowledge can be applied to increase the efficiency of recombinant protein expression.

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