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Decoding Post-Translational Modification Crosstalk With Proteomics

Post-translational modification (PTM) of proteins allows cells to regulate protein functions, transduce signals and respond to perturbations. PTMs expand protein functionality and diversity, which leads to increased proteome complexity. PTM crosstalk describes the combinatorial action of multiple PT...

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Detalles Bibliográficos
Autores principales: Leutert, Mario, Entwisle, Samuel W., Villén, Judit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430371/
https://www.ncbi.nlm.nih.gov/pubmed/34339852
http://dx.doi.org/10.1016/j.mcpro.2021.100129
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author Leutert, Mario
Entwisle, Samuel W.
Villén, Judit
author_facet Leutert, Mario
Entwisle, Samuel W.
Villén, Judit
author_sort Leutert, Mario
collection PubMed
description Post-translational modification (PTM) of proteins allows cells to regulate protein functions, transduce signals and respond to perturbations. PTMs expand protein functionality and diversity, which leads to increased proteome complexity. PTM crosstalk describes the combinatorial action of multiple PTMs on the same or on different proteins for higher order regulation. Here we review how recent advances in proteomic technologies, mass spectrometry instrumentation, and bioinformatics spurred the proteome-wide identification of PTM crosstalk through measurements of PTM sites. We provide an overview of the basic modes of PTM crosstalk, the proteomic methods to elucidate PTM crosstalk, and approaches that can inform about the functional consequences of PTM crosstalk.
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spelling pubmed-84303712021-09-13 Decoding Post-Translational Modification Crosstalk With Proteomics Leutert, Mario Entwisle, Samuel W. Villén, Judit Mol Cell Proteomics Review Post-translational modification (PTM) of proteins allows cells to regulate protein functions, transduce signals and respond to perturbations. PTMs expand protein functionality and diversity, which leads to increased proteome complexity. PTM crosstalk describes the combinatorial action of multiple PTMs on the same or on different proteins for higher order regulation. Here we review how recent advances in proteomic technologies, mass spectrometry instrumentation, and bioinformatics spurred the proteome-wide identification of PTM crosstalk through measurements of PTM sites. We provide an overview of the basic modes of PTM crosstalk, the proteomic methods to elucidate PTM crosstalk, and approaches that can inform about the functional consequences of PTM crosstalk. American Society for Biochemistry and Molecular Biology 2021-07-30 /pmc/articles/PMC8430371/ /pubmed/34339852 http://dx.doi.org/10.1016/j.mcpro.2021.100129 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Leutert, Mario
Entwisle, Samuel W.
Villén, Judit
Decoding Post-Translational Modification Crosstalk With Proteomics
title Decoding Post-Translational Modification Crosstalk With Proteomics
title_full Decoding Post-Translational Modification Crosstalk With Proteomics
title_fullStr Decoding Post-Translational Modification Crosstalk With Proteomics
title_full_unstemmed Decoding Post-Translational Modification Crosstalk With Proteomics
title_short Decoding Post-Translational Modification Crosstalk With Proteomics
title_sort decoding post-translational modification crosstalk with proteomics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430371/
https://www.ncbi.nlm.nih.gov/pubmed/34339852
http://dx.doi.org/10.1016/j.mcpro.2021.100129
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