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Small-molecule probes elucidate global enzyme activity in a proteomic context

The recent dramatic improvements in high-resolution mass spectrometry (MS) have revolutionized the speed and scope of proteomic studies. Conventional MS-based proteomics methodologies allow global protein profiling based on expression levels. Although these techniques are promising, there are numero...

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Autores principales: Lee, Jun-Seok, Yoo, Young-Hwa, Yoon, Chang No
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163878/
https://www.ncbi.nlm.nih.gov/pubmed/24499666
http://dx.doi.org/10.5483/BMBRep.2014.47.3.264
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author Lee, Jun-Seok
Yoo, Young-Hwa
Yoon, Chang No
author_facet Lee, Jun-Seok
Yoo, Young-Hwa
Yoon, Chang No
author_sort Lee, Jun-Seok
collection PubMed
description The recent dramatic improvements in high-resolution mass spectrometry (MS) have revolutionized the speed and scope of proteomic studies. Conventional MS-based proteomics methodologies allow global protein profiling based on expression levels. Although these techniques are promising, there are numerous biological activities yet to be unveiled, such as the dynamic regulation of enzyme activity. Chemical proteomics is an emerging field that extends these types proteomic profiling. In particular, activity-based protein profiling (ABPP) utilizes small-molecule probes to monitor enzyme activity directly in living intact subjects. In this mini-review, we summarize the unique roles of smallmolecule probes in proteomics studies and highlight some recent examples in which this principle has been applied. [BMB Reports 2014; 47(3): 149-157]
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spelling pubmed-41638782014-09-16 Small-molecule probes elucidate global enzyme activity in a proteomic context Lee, Jun-Seok Yoo, Young-Hwa Yoon, Chang No BMB Rep Review Article The recent dramatic improvements in high-resolution mass spectrometry (MS) have revolutionized the speed and scope of proteomic studies. Conventional MS-based proteomics methodologies allow global protein profiling based on expression levels. Although these techniques are promising, there are numerous biological activities yet to be unveiled, such as the dynamic regulation of enzyme activity. Chemical proteomics is an emerging field that extends these types proteomic profiling. In particular, activity-based protein profiling (ABPP) utilizes small-molecule probes to monitor enzyme activity directly in living intact subjects. In this mini-review, we summarize the unique roles of smallmolecule probes in proteomics studies and highlight some recent examples in which this principle has been applied. [BMB Reports 2014; 47(3): 149-157] Korean Society for Biochemistry and Molecular Biology 2014-03 /pmc/articles/PMC4163878/ /pubmed/24499666 http://dx.doi.org/10.5483/BMBRep.2014.47.3.264 Text en Copyright © 2014, Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lee, Jun-Seok
Yoo, Young-Hwa
Yoon, Chang No
Small-molecule probes elucidate global enzyme activity in a proteomic context
title Small-molecule probes elucidate global enzyme activity in a proteomic context
title_full Small-molecule probes elucidate global enzyme activity in a proteomic context
title_fullStr Small-molecule probes elucidate global enzyme activity in a proteomic context
title_full_unstemmed Small-molecule probes elucidate global enzyme activity in a proteomic context
title_short Small-molecule probes elucidate global enzyme activity in a proteomic context
title_sort small-molecule probes elucidate global enzyme activity in a proteomic context
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163878/
https://www.ncbi.nlm.nih.gov/pubmed/24499666
http://dx.doi.org/10.5483/BMBRep.2014.47.3.264
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