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Reversible phosphorylation of the 26S proteasome

The 26S proteasome at the center of the ubiquitin-proteasome system (UPS) is essential for virtually all cellular processes of eukaryotes. A common misconception about the proteasome is that, once made, it remains as a static and uniform complex with spontaneous and constitutive activity for protein...

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Detalles Bibliográficos
Autores principales: Guo, Xing, Huang, Xiuliang, Chen, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359188/
https://www.ncbi.nlm.nih.gov/pubmed/28258412
http://dx.doi.org/10.1007/s13238-017-0382-x
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author Guo, Xing
Huang, Xiuliang
Chen, Mark J.
author_facet Guo, Xing
Huang, Xiuliang
Chen, Mark J.
author_sort Guo, Xing
collection PubMed
description The 26S proteasome at the center of the ubiquitin-proteasome system (UPS) is essential for virtually all cellular processes of eukaryotes. A common misconception about the proteasome is that, once made, it remains as a static and uniform complex with spontaneous and constitutive activity for protein degradation. Recent discoveries have provided compelling evidence to support the exact opposite insomuch as the 26S proteasome undergoes dynamic and reversible phosphorylation under a variety of physiopathological conditions. In this review, we summarize the history and current understanding of proteasome phosphorylation, and advocate the idea of targeting proteasome kinases/phosphatases as a new strategy for clinical interventions of several human diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13238-017-0382-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-53591882017-04-03 Reversible phosphorylation of the 26S proteasome Guo, Xing Huang, Xiuliang Chen, Mark J. Protein Cell Review The 26S proteasome at the center of the ubiquitin-proteasome system (UPS) is essential for virtually all cellular processes of eukaryotes. A common misconception about the proteasome is that, once made, it remains as a static and uniform complex with spontaneous and constitutive activity for protein degradation. Recent discoveries have provided compelling evidence to support the exact opposite insomuch as the 26S proteasome undergoes dynamic and reversible phosphorylation under a variety of physiopathological conditions. In this review, we summarize the history and current understanding of proteasome phosphorylation, and advocate the idea of targeting proteasome kinases/phosphatases as a new strategy for clinical interventions of several human diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13238-017-0382-x) contains supplementary material, which is available to authorized users. Higher Education Press 2017-03-03 2017-04 /pmc/articles/PMC5359188/ /pubmed/28258412 http://dx.doi.org/10.1007/s13238-017-0382-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Guo, Xing
Huang, Xiuliang
Chen, Mark J.
Reversible phosphorylation of the 26S proteasome
title Reversible phosphorylation of the 26S proteasome
title_full Reversible phosphorylation of the 26S proteasome
title_fullStr Reversible phosphorylation of the 26S proteasome
title_full_unstemmed Reversible phosphorylation of the 26S proteasome
title_short Reversible phosphorylation of the 26S proteasome
title_sort reversible phosphorylation of the 26s proteasome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359188/
https://www.ncbi.nlm.nih.gov/pubmed/28258412
http://dx.doi.org/10.1007/s13238-017-0382-x
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