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Reading the glyco-code: New approaches to studying protein–carbohydrate interactions

The surface of all living cells is decorated with carbohydrate molecules. Hundreds of functional proteins bind to these glycosylated ligands; such binding events subsequently modulate many aspects of protein and cell function. Identifying ligands for glycan-binding proteins (GBPs) is a defining chal...

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Detalles Bibliográficos
Autores principales: Wisnovsky, Simon, Bertozzi, Carolyn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811956/
https://www.ncbi.nlm.nih.gov/pubmed/35653954
http://dx.doi.org/10.1016/j.sbi.2022.102395
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author Wisnovsky, Simon
Bertozzi, Carolyn R.
author_facet Wisnovsky, Simon
Bertozzi, Carolyn R.
author_sort Wisnovsky, Simon
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description The surface of all living cells is decorated with carbohydrate molecules. Hundreds of functional proteins bind to these glycosylated ligands; such binding events subsequently modulate many aspects of protein and cell function. Identifying ligands for glycan-binding proteins (GBPs) is a defining challenge of glycoscience research. Here, we review recent advances that are allowing protein-carbohydrate interactions to be dissected with an unprecedented level of precision. We specifically highlight how cell-based glycan arrays and glycogenomic profiling are being used to define the structural determinants of glycan-protein interactions in living cells. Going forward, these methods create exciting new opportunities for the study of glycans in physiology and disease.
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spelling pubmed-98119562023-01-04 Reading the glyco-code: New approaches to studying protein–carbohydrate interactions Wisnovsky, Simon Bertozzi, Carolyn R. Curr Opin Struct Biol Article The surface of all living cells is decorated with carbohydrate molecules. Hundreds of functional proteins bind to these glycosylated ligands; such binding events subsequently modulate many aspects of protein and cell function. Identifying ligands for glycan-binding proteins (GBPs) is a defining challenge of glycoscience research. Here, we review recent advances that are allowing protein-carbohydrate interactions to be dissected with an unprecedented level of precision. We specifically highlight how cell-based glycan arrays and glycogenomic profiling are being used to define the structural determinants of glycan-protein interactions in living cells. Going forward, these methods create exciting new opportunities for the study of glycans in physiology and disease. 2022-08 2022-05-30 /pmc/articles/PMC9811956/ /pubmed/35653954 http://dx.doi.org/10.1016/j.sbi.2022.102395 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons. (https://creativecommons.org/licenses/by/4.0/) org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Wisnovsky, Simon
Bertozzi, Carolyn R.
Reading the glyco-code: New approaches to studying protein–carbohydrate interactions
title Reading the glyco-code: New approaches to studying protein–carbohydrate interactions
title_full Reading the glyco-code: New approaches to studying protein–carbohydrate interactions
title_fullStr Reading the glyco-code: New approaches to studying protein–carbohydrate interactions
title_full_unstemmed Reading the glyco-code: New approaches to studying protein–carbohydrate interactions
title_short Reading the glyco-code: New approaches to studying protein–carbohydrate interactions
title_sort reading the glyco-code: new approaches to studying protein–carbohydrate interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811956/
https://www.ncbi.nlm.nih.gov/pubmed/35653954
http://dx.doi.org/10.1016/j.sbi.2022.102395
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