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Strategies to Target Specific Components of the Ubiquitin Conjugation/Deconjugation Machinery.

Authors :
Taylor NC
McGouran JF
Source :
Frontiers in chemistry [Front Chem] 2020 Jan 10; Vol. 7, pp. 914. Date of Electronic Publication: 2020 Jan 10 (Print Publication: 2019).
Publication Year :
2020

Abstract

The regulation of ubiquitination status in the cell is controlled by ubiquitin ligases acting in tandem with deubiquitinating enzymes. Ubiquitination controls many key processes in the cell from division to death making its tight regulation key to optimal cell function. Activity based protein profiling has emerged as a powerful technique to study these important enzymes. With around 100 deubiquitinating enzymes and 600 ubiquitin ligases in the human genome targeting a subclass of these enzymes or even a single enzyme is a compelling strategy to unpick this complex system. In this review we will discuss different approaches adopted, including activity-based probes centered around ubiquitin-protein, ubiquitin-peptide and mutated ubiquitin scaffolds. We examine challenges faced and opportunities presented to increase specificity in activity-based protein profiling of the ubiquitin conjugation/deconjugation machinery.<br /> (Copyright © 2020 Taylor and McGouran.)

Details

Language :
English
ISSN :
2296-2646
Volume :
7
Database :
MEDLINE
Journal :
Frontiers in chemistry
Publication Type :
Academic Journal
Accession number :
31998698
Full Text :
https://doi.org/10.3389/fchem.2019.00914