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Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites
O-GlcNAcylation, the addition of a single N-acetylglucosamine residue to serine and threonine residues of cytoplasmic, nuclear, or mitochondrial proteins, is a widespread regulatory posttranslational modification. It is involved in the response to nutritional status and stress, and its dysregulation...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724609/ https://www.ncbi.nlm.nih.gov/pubmed/32938750 http://dx.doi.org/10.1074/mcp.R120.002206 |
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author | Maynard, Jason C. Chalkley, Robert J. |
author_facet | Maynard, Jason C. Chalkley, Robert J. |
author_sort | Maynard, Jason C. |
collection | PubMed |
description | O-GlcNAcylation, the addition of a single N-acetylglucosamine residue to serine and threonine residues of cytoplasmic, nuclear, or mitochondrial proteins, is a widespread regulatory posttranslational modification. It is involved in the response to nutritional status and stress, and its dysregulation is associated with diseases ranging from Alzheimer’s to diabetes. Although the modification was first detected over 35 years ago, research into the function of O-GlcNAcylation has accelerated dramatically in the last 10 years owing to the development of new enrichment and mass spectrometry techniques that facilitate its analysis. This article summarizes methods for O-GlcNAc enrichment, key mass spectrometry instrumentation advancements, particularly those that allow modification site localization, and software tools that allow analysis of data from O-GlcNAc-modified peptides. |
format | Online Article Text |
id | pubmed-8724609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-87246092022-01-11 Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites Maynard, Jason C. Chalkley, Robert J. Mol Cell Proteomics Review O-GlcNAcylation, the addition of a single N-acetylglucosamine residue to serine and threonine residues of cytoplasmic, nuclear, or mitochondrial proteins, is a widespread regulatory posttranslational modification. It is involved in the response to nutritional status and stress, and its dysregulation is associated with diseases ranging from Alzheimer’s to diabetes. Although the modification was first detected over 35 years ago, research into the function of O-GlcNAcylation has accelerated dramatically in the last 10 years owing to the development of new enrichment and mass spectrometry techniques that facilitate its analysis. This article summarizes methods for O-GlcNAc enrichment, key mass spectrometry instrumentation advancements, particularly those that allow modification site localization, and software tools that allow analysis of data from O-GlcNAc-modified peptides. American Society for Biochemistry and Molecular Biology 2021-02-09 /pmc/articles/PMC8724609/ /pubmed/32938750 http://dx.doi.org/10.1074/mcp.R120.002206 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Maynard, Jason C. Chalkley, Robert J. Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites |
title | Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites |
title_full | Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites |
title_fullStr | Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites |
title_full_unstemmed | Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites |
title_short | Methods for Enrichment and Assignment of N-Acetylglucosamine Modification Sites |
title_sort | methods for enrichment and assignment of n-acetylglucosamine modification sites |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724609/ https://www.ncbi.nlm.nih.gov/pubmed/32938750 http://dx.doi.org/10.1074/mcp.R120.002206 |
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