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Aglycone sterics-selective enzymatic glycan remodeling
Precision remodeling of glycans in their native environments is pivotal for understanding glycan-mediated biological events and has important biotechnological implications in fields of clinical diagnosis, glyco-immune checkpoint therapy, and so forth. However, the influence of aglycone-steric divers...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249669/ https://www.ncbi.nlm.nih.gov/pubmed/35789841 http://dx.doi.org/10.1016/j.isci.2022.104578 |
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author | Mao, Anwen Zhang, Yan Wang, Guyu Zhong, Tong Chen, Xinyu Wang, Haiqi Xie, Ran Wang, Xiaojian Ding, Lin Ju, Huangxian |
author_facet | Mao, Anwen Zhang, Yan Wang, Guyu Zhong, Tong Chen, Xinyu Wang, Haiqi Xie, Ran Wang, Xiaojian Ding, Lin Ju, Huangxian |
author_sort | Mao, Anwen |
collection | PubMed |
description | Precision remodeling of glycans in their native environments is pivotal for understanding glycan-mediated biological events and has important biotechnological implications in fields of clinical diagnosis, glyco-immune checkpoint therapy, and so forth. However, the influence of aglycone-steric diversity on the selectivity of glycan remodeling has been largely overlooked, limiting the application in complex biological scenarios. Here, we report the achievement of aglycone sterics-selective enzymatic glycan remodeling by controlled grafting of functional polymers from glycoenzyme. Through tuning polymer length, a series of enzyme-polymer composites with varying substrate permeability are prepared, which afford an activity pattern-based differentiation strategy for aglycone sterics. This leads to the implementation of glycolipid’s partner screening, and aglycone sterics-selective glycan remodeling in a complex biological environment. We further orchestrate the polymer length adjustment with external cues to regulate aglycone-steric selectivity in a multi-faceted fashion, resulting in an unexpected enhancement of glycolipid remodeling, and temporal control of glycan remodeling on live cells. |
format | Online Article Text |
id | pubmed-9249669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92496692022-07-03 Aglycone sterics-selective enzymatic glycan remodeling Mao, Anwen Zhang, Yan Wang, Guyu Zhong, Tong Chen, Xinyu Wang, Haiqi Xie, Ran Wang, Xiaojian Ding, Lin Ju, Huangxian iScience Article Precision remodeling of glycans in their native environments is pivotal for understanding glycan-mediated biological events and has important biotechnological implications in fields of clinical diagnosis, glyco-immune checkpoint therapy, and so forth. However, the influence of aglycone-steric diversity on the selectivity of glycan remodeling has been largely overlooked, limiting the application in complex biological scenarios. Here, we report the achievement of aglycone sterics-selective enzymatic glycan remodeling by controlled grafting of functional polymers from glycoenzyme. Through tuning polymer length, a series of enzyme-polymer composites with varying substrate permeability are prepared, which afford an activity pattern-based differentiation strategy for aglycone sterics. This leads to the implementation of glycolipid’s partner screening, and aglycone sterics-selective glycan remodeling in a complex biological environment. We further orchestrate the polymer length adjustment with external cues to regulate aglycone-steric selectivity in a multi-faceted fashion, resulting in an unexpected enhancement of glycolipid remodeling, and temporal control of glycan remodeling on live cells. Elsevier 2022-06-13 /pmc/articles/PMC9249669/ /pubmed/35789841 http://dx.doi.org/10.1016/j.isci.2022.104578 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Mao, Anwen Zhang, Yan Wang, Guyu Zhong, Tong Chen, Xinyu Wang, Haiqi Xie, Ran Wang, Xiaojian Ding, Lin Ju, Huangxian Aglycone sterics-selective enzymatic glycan remodeling |
title | Aglycone sterics-selective enzymatic glycan remodeling |
title_full | Aglycone sterics-selective enzymatic glycan remodeling |
title_fullStr | Aglycone sterics-selective enzymatic glycan remodeling |
title_full_unstemmed | Aglycone sterics-selective enzymatic glycan remodeling |
title_short | Aglycone sterics-selective enzymatic glycan remodeling |
title_sort | aglycone sterics-selective enzymatic glycan remodeling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249669/ https://www.ncbi.nlm.nih.gov/pubmed/35789841 http://dx.doi.org/10.1016/j.isci.2022.104578 |
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