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Assay Systems for Profiling Deubiquitinating Activity

Deubiquitinating enzymes regulate various cellular processes, particularly protein degradation, localization, and protein–protein interactions. The dysregulation of deubiquitinating enzyme (DUB) activity has been linked to several diseases; however, the function of many DUBs has not been identified....

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Detalles Bibliográficos
Autores principales: Cho, Jinhong, Park, Jinyoung, Kim, Eunice EunKyeong, Song, Eun Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460613/
https://www.ncbi.nlm.nih.gov/pubmed/32781716
http://dx.doi.org/10.3390/ijms21165638
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author Cho, Jinhong
Park, Jinyoung
Kim, Eunice EunKyeong
Song, Eun Joo
author_facet Cho, Jinhong
Park, Jinyoung
Kim, Eunice EunKyeong
Song, Eun Joo
author_sort Cho, Jinhong
collection PubMed
description Deubiquitinating enzymes regulate various cellular processes, particularly protein degradation, localization, and protein–protein interactions. The dysregulation of deubiquitinating enzyme (DUB) activity has been linked to several diseases; however, the function of many DUBs has not been identified. Therefore, the development of methods to assess DUB activity is important to identify novel DUBs, characterize DUB selectivity, and profile dynamic DUB substrates. Here, we review various methods of evaluating DUB activity using cell lysates or purified DUBs, as well as the types of probes used in these methods. In addition, we introduce some techniques that can deliver DUB probes into the cells and cell-permeable activity-based probes to directly visualize and quantify DUB activity in live cells. This review could contribute to the development of DUB inhibitors by providing important information on the characteristics and applications of various probes used to evaluate and detect DUB activity in vitro and in vivo.
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spelling pubmed-74606132020-09-03 Assay Systems for Profiling Deubiquitinating Activity Cho, Jinhong Park, Jinyoung Kim, Eunice EunKyeong Song, Eun Joo Int J Mol Sci Review Deubiquitinating enzymes regulate various cellular processes, particularly protein degradation, localization, and protein–protein interactions. The dysregulation of deubiquitinating enzyme (DUB) activity has been linked to several diseases; however, the function of many DUBs has not been identified. Therefore, the development of methods to assess DUB activity is important to identify novel DUBs, characterize DUB selectivity, and profile dynamic DUB substrates. Here, we review various methods of evaluating DUB activity using cell lysates or purified DUBs, as well as the types of probes used in these methods. In addition, we introduce some techniques that can deliver DUB probes into the cells and cell-permeable activity-based probes to directly visualize and quantify DUB activity in live cells. This review could contribute to the development of DUB inhibitors by providing important information on the characteristics and applications of various probes used to evaluate and detect DUB activity in vitro and in vivo. MDPI 2020-08-06 /pmc/articles/PMC7460613/ /pubmed/32781716 http://dx.doi.org/10.3390/ijms21165638 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cho, Jinhong
Park, Jinyoung
Kim, Eunice EunKyeong
Song, Eun Joo
Assay Systems for Profiling Deubiquitinating Activity
title Assay Systems for Profiling Deubiquitinating Activity
title_full Assay Systems for Profiling Deubiquitinating Activity
title_fullStr Assay Systems for Profiling Deubiquitinating Activity
title_full_unstemmed Assay Systems for Profiling Deubiquitinating Activity
title_short Assay Systems for Profiling Deubiquitinating Activity
title_sort assay systems for profiling deubiquitinating activity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460613/
https://www.ncbi.nlm.nih.gov/pubmed/32781716
http://dx.doi.org/10.3390/ijms21165638
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