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Chemical reporters to study mammalian O-glycosylation

Glycans play essential roles in a range of cellular processes and have been shown to contribute to various pathologies. The diversity and dynamic nature of glycan structures and the complexities of glycan biosynthetic pathways make it challenging to study the roles of specific glycans in normal cell...

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Detalles Bibliográficos
Autores principales: Huxley, Kathryn E., Willems, Lianne I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106504/
https://www.ncbi.nlm.nih.gov/pubmed/33860782
http://dx.doi.org/10.1042/BST20200839
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author Huxley, Kathryn E.
Willems, Lianne I.
author_facet Huxley, Kathryn E.
Willems, Lianne I.
author_sort Huxley, Kathryn E.
collection PubMed
description Glycans play essential roles in a range of cellular processes and have been shown to contribute to various pathologies. The diversity and dynamic nature of glycan structures and the complexities of glycan biosynthetic pathways make it challenging to study the roles of specific glycans in normal cellular function and disease. Chemical reporters have emerged as powerful tools to characterise glycan structures and monitor dynamic changes in glycan levels in a native context. A variety of tags can be introduced onto specific monosaccharides via the chemical modification of endogenous glycan structures or by metabolic or enzymatic incorporation of unnatural monosaccharides into cellular glycans. These chemical reporter strategies offer unique opportunities to study and manipulate glycan functions in living cells or whole organisms. In this review, we discuss recent advances in metabolic oligosaccharide engineering and chemoenzymatic glycan labelling, focusing on their application to the study of mammalian O-linked glycans. We describe current barriers to achieving glycan labelling specificity and highlight innovations that have started to pave the way to overcome these challenges.
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spelling pubmed-81065042021-05-18 Chemical reporters to study mammalian O-glycosylation Huxley, Kathryn E. Willems, Lianne I. Biochem Soc Trans Review Articles Glycans play essential roles in a range of cellular processes and have been shown to contribute to various pathologies. The diversity and dynamic nature of glycan structures and the complexities of glycan biosynthetic pathways make it challenging to study the roles of specific glycans in normal cellular function and disease. Chemical reporters have emerged as powerful tools to characterise glycan structures and monitor dynamic changes in glycan levels in a native context. A variety of tags can be introduced onto specific monosaccharides via the chemical modification of endogenous glycan structures or by metabolic or enzymatic incorporation of unnatural monosaccharides into cellular glycans. These chemical reporter strategies offer unique opportunities to study and manipulate glycan functions in living cells or whole organisms. In this review, we discuss recent advances in metabolic oligosaccharide engineering and chemoenzymatic glycan labelling, focusing on their application to the study of mammalian O-linked glycans. We describe current barriers to achieving glycan labelling specificity and highlight innovations that have started to pave the way to overcome these challenges. Portland Press Ltd. 2021-04-30 2021-04-16 /pmc/articles/PMC8106504/ /pubmed/33860782 http://dx.doi.org/10.1042/BST20200839 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of York in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC.
spellingShingle Review Articles
Huxley, Kathryn E.
Willems, Lianne I.
Chemical reporters to study mammalian O-glycosylation
title Chemical reporters to study mammalian O-glycosylation
title_full Chemical reporters to study mammalian O-glycosylation
title_fullStr Chemical reporters to study mammalian O-glycosylation
title_full_unstemmed Chemical reporters to study mammalian O-glycosylation
title_short Chemical reporters to study mammalian O-glycosylation
title_sort chemical reporters to study mammalian o-glycosylation
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106504/
https://www.ncbi.nlm.nih.gov/pubmed/33860782
http://dx.doi.org/10.1042/BST20200839
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