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Mass Spectrometry-Based Discovery of in vitro Kinome Substrates
Protein phosphorylation mediated by protein kinases is one of the most significant posttranslational modifications in many biological events. The function and physiological substrates of specific protein kinases, which are highly associated with known signal transduction elements or therapeutic targ...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Mass Spectrometry Society of Japan
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242781/ https://www.ncbi.nlm.nih.gov/pubmed/32547896 http://dx.doi.org/10.5702/massspectrometry.A0082 |
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author | Sugiyama, Naoyuki |
author_facet | Sugiyama, Naoyuki |
author_sort | Sugiyama, Naoyuki |
collection | PubMed |
description | Protein phosphorylation mediated by protein kinases is one of the most significant posttranslational modifications in many biological events. The function and physiological substrates of specific protein kinases, which are highly associated with known signal transduction elements or therapeutic targets, have been extensively studied using various approaches; however, most protein kinases have not yet been characterized. In recent decades, many techniques have been developed for the identification of in vitro and physiological substrates of protein kinases. In this review, I summarize recent studies profiling the characteristics of kinases using mass spectrometry-based proteomics, focusing on the large-scale identification of in vitro substrates of the human kinome using a quantitative phosphoproteomics approach. |
format | Online Article Text |
id | pubmed-7242781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Mass Spectrometry Society of Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-72427812020-06-15 Mass Spectrometry-Based Discovery of in vitro Kinome Substrates Sugiyama, Naoyuki Mass Spectrom (Tokyo) Review Protein phosphorylation mediated by protein kinases is one of the most significant posttranslational modifications in many biological events. The function and physiological substrates of specific protein kinases, which are highly associated with known signal transduction elements or therapeutic targets, have been extensively studied using various approaches; however, most protein kinases have not yet been characterized. In recent decades, many techniques have been developed for the identification of in vitro and physiological substrates of protein kinases. In this review, I summarize recent studies profiling the characteristics of kinases using mass spectrometry-based proteomics, focusing on the large-scale identification of in vitro substrates of the human kinome using a quantitative phosphoproteomics approach. The Mass Spectrometry Society of Japan 2020 2020-03-28 /pmc/articles/PMC7242781/ /pubmed/32547896 http://dx.doi.org/10.5702/massspectrometry.A0082 Text en Copyright © 2020 Naoyuki Sugiyama. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Sugiyama, Naoyuki Mass Spectrometry-Based Discovery of in vitro Kinome Substrates |
title | Mass Spectrometry-Based Discovery of in vitro Kinome Substrates |
title_full | Mass Spectrometry-Based Discovery of in vitro Kinome Substrates |
title_fullStr | Mass Spectrometry-Based Discovery of in vitro Kinome Substrates |
title_full_unstemmed | Mass Spectrometry-Based Discovery of in vitro Kinome Substrates |
title_short | Mass Spectrometry-Based Discovery of in vitro Kinome Substrates |
title_sort | mass spectrometry-based discovery of in vitro kinome substrates |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242781/ https://www.ncbi.nlm.nih.gov/pubmed/32547896 http://dx.doi.org/10.5702/massspectrometry.A0082 |
work_keys_str_mv | AT sugiyamanaoyuki massspectrometrybaseddiscoveryofinvitrokinomesubstrates |