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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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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. |
format | Online Article Text |
id | pubmed-10453990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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