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Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources
Mass spectrometry-based phosphoproteomics is becoming an essential methodology for the study of global cellular signaling. Numerous bioinformatics resources are available to facilitate the translation of phosphopeptide identification and quantification results into novel biological and clinical insi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353784/ https://www.ncbi.nlm.nih.gov/pubmed/32676006 http://dx.doi.org/10.1186/s12014-020-09290-x |
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author | Savage, Sara R. Zhang, Bing |
author_facet | Savage, Sara R. Zhang, Bing |
author_sort | Savage, Sara R. |
collection | PubMed |
description | Mass spectrometry-based phosphoproteomics is becoming an essential methodology for the study of global cellular signaling. Numerous bioinformatics resources are available to facilitate the translation of phosphopeptide identification and quantification results into novel biological and clinical insights, a critical step in phosphoproteomics data analysis. These resources include knowledge bases of kinases and phosphatases, phosphorylation sites, kinase inhibitors, and sequence variants affecting kinase function, and bioinformatics tools that can predict phosphorylation sites in addition to the kinase that phosphorylates them, infer kinase activity, and predict the effect of mutations on kinase signaling. However, these resources exist in silos and it is challenging to select among multiple resources with similar functions. Therefore, we put together a comprehensive collection of resources related to phosphoproteomics data interpretation, compared the use of tools with similar functions, and assessed the usability from the standpoint of typical biologists or clinicians. Overall, tools could be improved by standardization of enzyme names, flexibility of data input and output format, consistent maintenance, and detailed manuals. |
format | Online Article Text |
id | pubmed-7353784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73537842020-07-15 Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources Savage, Sara R. Zhang, Bing Clin Proteomics Review Mass spectrometry-based phosphoproteomics is becoming an essential methodology for the study of global cellular signaling. Numerous bioinformatics resources are available to facilitate the translation of phosphopeptide identification and quantification results into novel biological and clinical insights, a critical step in phosphoproteomics data analysis. These resources include knowledge bases of kinases and phosphatases, phosphorylation sites, kinase inhibitors, and sequence variants affecting kinase function, and bioinformatics tools that can predict phosphorylation sites in addition to the kinase that phosphorylates them, infer kinase activity, and predict the effect of mutations on kinase signaling. However, these resources exist in silos and it is challenging to select among multiple resources with similar functions. Therefore, we put together a comprehensive collection of resources related to phosphoproteomics data interpretation, compared the use of tools with similar functions, and assessed the usability from the standpoint of typical biologists or clinicians. Overall, tools could be improved by standardization of enzyme names, flexibility of data input and output format, consistent maintenance, and detailed manuals. BioMed Central 2020-07-11 /pmc/articles/PMC7353784/ /pubmed/32676006 http://dx.doi.org/10.1186/s12014-020-09290-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Savage, Sara R. Zhang, Bing Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
title | Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
title_full | Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
title_fullStr | Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
title_full_unstemmed | Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
title_short | Using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
title_sort | using phosphoproteomics data to understand cellular signaling: a comprehensive guide to bioinformatics resources |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353784/ https://www.ncbi.nlm.nih.gov/pubmed/32676006 http://dx.doi.org/10.1186/s12014-020-09290-x |
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