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Updated: Mar 6, 2026

Identification of Post-translational Modifications of Plant Protein Complexes
Published on: February 22, 2014
Reversible phosphorylation of the 26S proteasome
Xing Guo1, Xiuliang Huang2, Mark J Chen3
1The Life Sciences Institute of Zhejiang University, Hangzhou, 310058, China. xguo@zju.edu.cn.
Abstract:
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.
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