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The NMR studies of CMP inhibition of polysialylation

The overexpression of polysialic acid (polySia) on neural cell adhesion molecules (NCAM) promotes hypersialylation, and thus benefits cancer cell migration and invasion. It has been proposed that the binding between the polysialyltransferase domain (PSTD) and CMP-Sia needs to be inhibited in order t...

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Autores principales: Lu, Bo, Liao, Si-Ming, Liu, Xue-Hui, Liang, Shi-Jie, Huang, Jun, Lin, Mei, Meng, Li, Wang, Qing-Yan, Huang, Ri-Bo, Zhou, Guo-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453990/
https://www.ncbi.nlm.nih.gov/pubmed/37615033
http://dx.doi.org/10.1080/14756366.2023.2248411
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author Lu, Bo
Liao, Si-Ming
Liu, Xue-Hui
Liang, Shi-Jie
Huang, Jun
Lin, Mei
Meng, Li
Wang, Qing-Yan
Huang, Ri-Bo
Zhou, Guo-Ping
author_facet Lu, Bo
Liao, Si-Ming
Liu, Xue-Hui
Liang, Shi-Jie
Huang, Jun
Lin, Mei
Meng, Li
Wang, Qing-Yan
Huang, Ri-Bo
Zhou, Guo-Ping
author_sort Lu, Bo
collection PubMed
description The overexpression of polysialic acid (polySia) on neural cell adhesion molecules (NCAM) promotes hypersialylation, and thus benefits cancer cell migration and invasion. It has been proposed that the binding between the polysialyltransferase domain (PSTD) and CMP-Sia needs to be inhibited in order to block the effects of hypersialylation. In this study, CMP was confirmed to be a competitive inhibitor of polysialyltransferases (polySTs) in the presence of CMP-Sia and triSia (oligosialic acid trimer) based on the interactional features between molecules. The further NMR analysis suggested that polysialylation could be partially inhibited when CMP-Sia and polySia co-exist in solution. In addition, an unexpecting finding is that CMP-Sia plays a role in reducing the gathering extent of polySia chains on the PSTD, and may benefit for the inhibition of polysialylation. The findings in this study may provide new insight into the optimal design of the drug and inhibitor for cancer treatment.
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spelling pubmed-104539902023-08-26 The NMR studies of CMP inhibition of polysialylation Lu, Bo Liao, Si-Ming Liu, Xue-Hui Liang, Shi-Jie Huang, Jun Lin, Mei Meng, Li Wang, Qing-Yan Huang, Ri-Bo Zhou, Guo-Ping J Enzyme Inhib Med Chem Research Article The overexpression of polysialic acid (polySia) on neural cell adhesion molecules (NCAM) promotes hypersialylation, and thus benefits cancer cell migration and invasion. It has been proposed that the binding between the polysialyltransferase domain (PSTD) and CMP-Sia needs to be inhibited in order to block the effects of hypersialylation. In this study, CMP was confirmed to be a competitive inhibitor of polysialyltransferases (polySTs) in the presence of CMP-Sia and triSia (oligosialic acid trimer) based on the interactional features between molecules. The further NMR analysis suggested that polysialylation could be partially inhibited when CMP-Sia and polySia co-exist in solution. In addition, an unexpecting finding is that CMP-Sia plays a role in reducing the gathering extent of polySia chains on the PSTD, and may benefit for the inhibition of polysialylation. The findings in this study may provide new insight into the optimal design of the drug and inhibitor for cancer treatment. Taylor & Francis 2023-08-24 /pmc/articles/PMC10453990/ /pubmed/37615033 http://dx.doi.org/10.1080/14756366.2023.2248411 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Article
Lu, Bo
Liao, Si-Ming
Liu, Xue-Hui
Liang, Shi-Jie
Huang, Jun
Lin, Mei
Meng, Li
Wang, Qing-Yan
Huang, Ri-Bo
Zhou, Guo-Ping
The NMR studies of CMP inhibition of polysialylation
title The NMR studies of CMP inhibition of polysialylation
title_full The NMR studies of CMP inhibition of polysialylation
title_fullStr The NMR studies of CMP inhibition of polysialylation
title_full_unstemmed The NMR studies of CMP inhibition of polysialylation
title_short The NMR studies of CMP inhibition of polysialylation
title_sort nmr studies of cmp inhibition of polysialylation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453990/
https://www.ncbi.nlm.nih.gov/pubmed/37615033
http://dx.doi.org/10.1080/14756366.2023.2248411
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