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Catching a DUB in the act: novel ubiquitin-based active site directed probes

Protein ubiquitylation is an important regulator of protein function, localization and half-life. It plays a key role in most cellular processes including immune signaling. Deregulation of this process is a major causative factor for many diseases. A major advancement in the identification and chara...

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Detalles Bibliográficos
Autores principales: Ekkebus, Reggy, Flierman, Dennis, Geurink, Paul P, Ovaa, Huib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185813/
https://www.ncbi.nlm.nih.gov/pubmed/25461387
http://dx.doi.org/10.1016/j.cbpa.2014.10.005
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author Ekkebus, Reggy
Flierman, Dennis
Geurink, Paul P
Ovaa, Huib
author_facet Ekkebus, Reggy
Flierman, Dennis
Geurink, Paul P
Ovaa, Huib
author_sort Ekkebus, Reggy
collection PubMed
description Protein ubiquitylation is an important regulator of protein function, localization and half-life. It plays a key role in most cellular processes including immune signaling. Deregulation of this process is a major causative factor for many diseases. A major advancement in the identification and characterization of the enzymes that remove ubiquitin, deubiquitylases (DUBs) was made by the development of activity-based probes (ABPs). Recent advances in chemical protein synthesis and ligation methodology has yielded novel reagents for use in ubiquitylation research. We describe recent advances and discuss future directions in reagent development for studying DUBs.
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spelling pubmed-71858132020-04-28 Catching a DUB in the act: novel ubiquitin-based active site directed probes Ekkebus, Reggy Flierman, Dennis Geurink, Paul P Ovaa, Huib Curr Opin Chem Biol Article Protein ubiquitylation is an important regulator of protein function, localization and half-life. It plays a key role in most cellular processes including immune signaling. Deregulation of this process is a major causative factor for many diseases. A major advancement in the identification and characterization of the enzymes that remove ubiquitin, deubiquitylases (DUBs) was made by the development of activity-based probes (ABPs). Recent advances in chemical protein synthesis and ligation methodology has yielded novel reagents for use in ubiquitylation research. We describe recent advances and discuss future directions in reagent development for studying DUBs. Elsevier Ltd. 2014-12 2014-11-03 /pmc/articles/PMC7185813/ /pubmed/25461387 http://dx.doi.org/10.1016/j.cbpa.2014.10.005 Text en Copyright © 2014 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ekkebus, Reggy
Flierman, Dennis
Geurink, Paul P
Ovaa, Huib
Catching a DUB in the act: novel ubiquitin-based active site directed probes
title Catching a DUB in the act: novel ubiquitin-based active site directed probes
title_full Catching a DUB in the act: novel ubiquitin-based active site directed probes
title_fullStr Catching a DUB in the act: novel ubiquitin-based active site directed probes
title_full_unstemmed Catching a DUB in the act: novel ubiquitin-based active site directed probes
title_short Catching a DUB in the act: novel ubiquitin-based active site directed probes
title_sort catching a dub in the act: novel ubiquitin-based active site directed probes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185813/
https://www.ncbi.nlm.nih.gov/pubmed/25461387
http://dx.doi.org/10.1016/j.cbpa.2014.10.005
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