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Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation
Protein O-GlcNAcylation is a non-canonical glycosylation of nuclear, mitochondrial, and cytoplasmic proteins with the attachment of a single O-linked β-N-acetyl-glucosamine (O-GlcNAc) moiety. Advances in labeling and identifying O-GlcNAcylated proteins have helped improve the understanding of O-GlcN...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222402/ https://www.ncbi.nlm.nih.gov/pubmed/30241321 http://dx.doi.org/10.3390/molecules23102411 |
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author | Kim, Eun Ju |
author_facet | Kim, Eun Ju |
author_sort | Kim, Eun Ju |
collection | PubMed |
description | Protein O-GlcNAcylation is a non-canonical glycosylation of nuclear, mitochondrial, and cytoplasmic proteins with the attachment of a single O-linked β-N-acetyl-glucosamine (O-GlcNAc) moiety. Advances in labeling and identifying O-GlcNAcylated proteins have helped improve the understanding of O-GlcNAcylation at levels that range from basic molecular biology to cell signaling and gene regulation to physiology and disease. This review describes these advances in chemistry involving chemical reporters and their bioorthogonal reactions utilized for detection and construction of O-GlcNAc proteomes in a molecular mechanistic view. This detailed view will help better understand the principles of the chemistries utilized for biology discovery and promote continued efforts in developing new molecular tools and new strategies to further explore protein O-GlcNAcylation. |
format | Online Article Text |
id | pubmed-6222402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62224022018-11-13 Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation Kim, Eun Ju Molecules Review Protein O-GlcNAcylation is a non-canonical glycosylation of nuclear, mitochondrial, and cytoplasmic proteins with the attachment of a single O-linked β-N-acetyl-glucosamine (O-GlcNAc) moiety. Advances in labeling and identifying O-GlcNAcylated proteins have helped improve the understanding of O-GlcNAcylation at levels that range from basic molecular biology to cell signaling and gene regulation to physiology and disease. This review describes these advances in chemistry involving chemical reporters and their bioorthogonal reactions utilized for detection and construction of O-GlcNAc proteomes in a molecular mechanistic view. This detailed view will help better understand the principles of the chemistries utilized for biology discovery and promote continued efforts in developing new molecular tools and new strategies to further explore protein O-GlcNAcylation. MDPI 2018-09-20 /pmc/articles/PMC6222402/ /pubmed/30241321 http://dx.doi.org/10.3390/molecules23102411 Text en © 2018 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kim, Eun Ju Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation |
title | Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation |
title_full | Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation |
title_fullStr | Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation |
title_full_unstemmed | Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation |
title_short | Chemical Reporters and Their Bioorthogonal Reactions for Labeling Protein O-GlcNAcylation |
title_sort | chemical reporters and their bioorthogonal reactions for labeling protein o-glcnacylation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222402/ https://www.ncbi.nlm.nih.gov/pubmed/30241321 http://dx.doi.org/10.3390/molecules23102411 |
work_keys_str_mv | AT kimeunju chemicalreportersandtheirbioorthogonalreactionsforlabelingproteinoglcnacylation |