Peripheral Protein Quality Control Removes Unfolded CFTR from the Plasma Membrane
Open accessAbstract
Peripheral Quality Control: Protein misfolding diseases often lead to the retention and degradation of important proteins within the endoplasmic reticulum (ER). Strategies to reduce the stringency of ER quality control that allow the proteins to carry on through the secretory pathway to reach their destination at the cell surface have shown some promise. Okiyoneda et al. (p. 805 , published online 1 July; see the Perspective by Hutt and Balch ) wanted to understand how, even if a protein reaches its destination, it may still be subjected to a second level of quality control and be cleared from the plasma membrane. Using functional small-interfering RNA screens in cells expressing the common cystic fibrosis mutation F508CFTR, the authors identified a pair of chaperones that promoted clearance of defective proteins from the plasma membrane. This peripheral quality-control step will also need to be overcome to increase the effectiveness of strategies to overcome protein misfolding disorders.
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F508del leads to severely impaired processing, plasma membrane expression, and stability, as well as defective gating of F508del-CFTR.
“This leads to a combination of defects, consisting of severely impaired processing, plasma membrane (PM) expression, and stability, as well as defective gating of the F508del-CFTR (12–14).”
From Allosteric folding correction of F508del and rare CFTR mutants by elexacaftor-tezacaftor-ivacaftor (Trikafta) combination (2020) · cites this paper as [13]
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Veit, G., Roldan, A., Hancock, M. A., Da Fonte, D. F., Xu, H., Hussein, M., Frenkiel, S., Matouk, E., Velkov, T., & Lukacs, G. L. (2020) · JCI Insight · doi:10.1172/jci.insight.139983 · Cited by 250 · see citing works
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Zhang, K., Li, Z., Jaiswal, M., Bayat, V., Xiong, B., Sandoval, H., Charng, W.-L., David, G., Haueter, C., Yamamoto, S., et al. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201208033 · Cited by 58 · see citing works
- Authors
- Okiyoneda, T., Barrière, H., Bagdány, M., Rabeh, W. M., Du, K., Höhfeld, J., Young, J. C., & Lukacs, G. L.
- Affiliations
- McGill University (CA)
- University of Bonn (DE)
- Department of Physiology, and Groupe de Recherche Axé sur la Structure des Protéine (GRASP) McGill University, Montreal, Quebec H3G 1Y6, Canada.
- Venue
- Science
- Published
- 2010-08-13
- Volume
- 329
- Issue
- 5993
- Pages
- 805-810
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5026491
- OpenAlex
- W1982956224
- Cited by
- 408
- References
- 0
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 11 · 2023: 20 · 2022: 20 · 2021: 21 · 2020: 29 · 2019: 27 · 2018: 30 · 2017: 26 · 2016: 25 · 2015: 29 · 2014: 31 · 2013: 29 · 2012: 39
- FWCI
- 29.75
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Public Health Service (70306-1, 68825-2, 103329-1)
- Canadian Institutes of Health Research (68825_2, 103329_1, 70306_1)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- CFTR, cystic fibrosis, protein quality control, ubiquitination, lysosomal degradation, protein internalization, molecular chaperones, co-chaperones, ubiquitin ligase, E2 ubiquitin-conjugating enzyme, membrane protein degradation, endoplasmic reticulum quality control
- MeSH terms
- Cell Membrane, Glycosylation, HeLa Cells, Homeostasis, Humans, Lysosomes, Protein Conformation, Recombinant Proteins, Temperature, Protein Folding, Molecular Chaperones, HSP90 Heat-Shock Proteins, Cystic Fibrosis Transmembrane Conductance Regulator, Protein Transport, RNA, Small Interfering, Ubiquitin-Protein Ligases, Mutant Proteins, HSC70 Heat-Shock Proteins, Ubiquitination, Protein Stability, Ubiquitinated Proteins
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