Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Sugiyama, Naoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mass Spectrometry Society of Japan 2020
Materias:
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
_version_ 1783537297294098432
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