Active-site directed probes to report enzymatic action in the ubiquitin proteasome system
- 19 July 2007
- journal article
- Published by Springer Nature in Nature Reviews Cancer
- Vol. 7 (8) , 613-620
- https://doi.org/10.1038/nrc2128
Abstract
Irreversible covalent inhibitors equipped with reporter groups allow the study of target enzymes based on catalytic activity instead of expression level. This Perspective discusses the design and use of such probes directed at the ubiquitin–proteasome system. Can they identify new cancer therapies that target this system? Irreversible covalent inhibitors equipped with reporter groups, also termed activity-based probes, allow the study of target enzymes based on catalytic activity instead of expression level, which does not necessarily indicate protein function and subsequent cellular consequences. Activity-based probes offer advantages over traditional techniques: they can be applied to the cell or tissue of choice and molecular imaging and pharmacology applications are possible. Here the design and use of probes directed at enzymatic activities in the ubiquitin proteasome system are discussed. This system holds promise for the development of new, targeted anticancer therapies and the probes discussed here might aid in fulfilling this promise.Keywords
This publication has 99 references indexed in Scilit:
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsNature, 2007
- Identification of a Peptoid Inhibitor of the Proteasome 19S Regulatory ParticleJournal of the American Chemical Society, 2007
- The deubiquitinating enzyme USP2a regulates the p53 pathway by targeting Mdm2The EMBO Journal, 2007
- Drug discovery in the ubiquitin–proteasome systemNature Reviews Drug Discovery, 2006
- Ubiquitylation and cell signalingThe EMBO Journal, 2005
- Small molecule RITA binds to p53, blocks p53–HDM-2 interaction and activates p53 function in tumorsNature Medicine, 2004
- De-ubiquitination and ubiquitin ligase domains of A20 downregulate NF-κB signallingNature, 2004
- Disruption of HAUSP gene stabilizes p53Nature, 2004
- A cryptic protease couples deubiquitination and degradation by the proteasomeNature, 2002
- Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilizationNature, 2002