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Carbohydrate microarrays for screening functional glycans

Carbohydrate microarrays have become robust and powerful tools for the rapid analysis of glycan-associated binding events. However, this microarray technology has rarely been applied in studies of glycan-mediated cellular responses. Herein we describe a carbohydrate microarray-based approach for the...

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Autores principales: Pai, Jaeyoung, Hyun, Ji Young, Jeong, Jieun, Loh, Sohee, Cho, Eun-Hee, Kang, Young-Sun, Shin, Injae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968531/
https://www.ncbi.nlm.nih.gov/pubmed/29899934
http://dx.doi.org/10.1039/c5sc03789a
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author Pai, Jaeyoung
Hyun, Ji Young
Jeong, Jieun
Loh, Sohee
Cho, Eun-Hee
Kang, Young-Sun
Shin, Injae
author_facet Pai, Jaeyoung
Hyun, Ji Young
Jeong, Jieun
Loh, Sohee
Cho, Eun-Hee
Kang, Young-Sun
Shin, Injae
author_sort Pai, Jaeyoung
collection PubMed
description Carbohydrate microarrays have become robust and powerful tools for the rapid analysis of glycan-associated binding events. However, this microarray technology has rarely been applied in studies of glycan-mediated cellular responses. Herein we describe a carbohydrate microarray-based approach for the rapid screening of biologically active glycans that stimulate the production of reactive oxygen species (ROS) through binding to the cell-surface lectin. We employed a microarray assay and a fluorescent ROS probe to identify the functional glycans which enhance ROS production. Cells binding to glycans on the microarrays produced ROS, whose levels were decreased in the presence of a ROS scavenger or a NADPH oxidase inhibitor. The present study leads us to suggest that glycan microarrays are applicable to the simultaneous screening of various glycans whose binding to the cell-surface lectin elicits cellular response.
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spelling pubmed-59685312018-06-13 Carbohydrate microarrays for screening functional glycans Pai, Jaeyoung Hyun, Ji Young Jeong, Jieun Loh, Sohee Cho, Eun-Hee Kang, Young-Sun Shin, Injae Chem Sci Chemistry Carbohydrate microarrays have become robust and powerful tools for the rapid analysis of glycan-associated binding events. However, this microarray technology has rarely been applied in studies of glycan-mediated cellular responses. Herein we describe a carbohydrate microarray-based approach for the rapid screening of biologically active glycans that stimulate the production of reactive oxygen species (ROS) through binding to the cell-surface lectin. We employed a microarray assay and a fluorescent ROS probe to identify the functional glycans which enhance ROS production. Cells binding to glycans on the microarrays produced ROS, whose levels were decreased in the presence of a ROS scavenger or a NADPH oxidase inhibitor. The present study leads us to suggest that glycan microarrays are applicable to the simultaneous screening of various glycans whose binding to the cell-surface lectin elicits cellular response. Royal Society of Chemistry 2016-03-01 2016-01-05 /pmc/articles/PMC5968531/ /pubmed/29899934 http://dx.doi.org/10.1039/c5sc03789a Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Pai, Jaeyoung
Hyun, Ji Young
Jeong, Jieun
Loh, Sohee
Cho, Eun-Hee
Kang, Young-Sun
Shin, Injae
Carbohydrate microarrays for screening functional glycans
title Carbohydrate microarrays for screening functional glycans
title_full Carbohydrate microarrays for screening functional glycans
title_fullStr Carbohydrate microarrays for screening functional glycans
title_full_unstemmed Carbohydrate microarrays for screening functional glycans
title_short Carbohydrate microarrays for screening functional glycans
title_sort carbohydrate microarrays for screening functional glycans
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968531/
https://www.ncbi.nlm.nih.gov/pubmed/29899934
http://dx.doi.org/10.1039/c5sc03789a
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