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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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Autor principal: Kim, Eun Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
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.
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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
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