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Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection
Neurotoxicity of organophosphate compounds (OPs) can catastrophically cause nervous system injury by inhibiting acetylcholinesterase (AChE) expression. Although artificial systems have been developed for indirect neuroprotection, they are limited to dissociating P-O bonds for eliminating OPs. Howeve...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539540/ https://www.ncbi.nlm.nih.gov/pubmed/37770453 http://dx.doi.org/10.1038/s41467-023-41765-x |
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author | Xu, Weiqing Cai, Xiaoli Wu, Yu Wen, Yating Su, Rina Zhang, Yu Huang, Yuteng Zheng, Qihui Hu, Liuyong Cui, Xiaowen Zheng, Lirong Zhang, Shipeng Gu, Wenling Song, Weiyu Guo, Shaojun Zhu, Chengzhou |
author_facet | Xu, Weiqing Cai, Xiaoli Wu, Yu Wen, Yating Su, Rina Zhang, Yu Huang, Yuteng Zheng, Qihui Hu, Liuyong Cui, Xiaowen Zheng, Lirong Zhang, Shipeng Gu, Wenling Song, Weiyu Guo, Shaojun Zhu, Chengzhou |
author_sort | Xu, Weiqing |
collection | PubMed |
description | Neurotoxicity of organophosphate compounds (OPs) can catastrophically cause nervous system injury by inhibiting acetylcholinesterase (AChE) expression. Although artificial systems have been developed for indirect neuroprotection, they are limited to dissociating P-O bonds for eliminating OPs. However, these systems have failed to overcome the deactivation of AChE. Herein, we report our finding that Al(3+) is engineered onto the nodes of metal–organic framework to synthesize MOF-808-Al with enhanced Lewis acidity. The resultant MOF-808-Al efficiently mimics the catalytic behavior of AChE and has a self-defense ability to break the activity inhibition by OPs. Mechanism investigations elucidate that Al(3+) Lewis acid sites with a strong polarization effect unite the highly electronegative –OH groups to form the enzyme-like catalytic center, resulting in superior substrate activation and nucleophilic attack ability with a 2.7-fold activity improvement. The multifunctional MOF-808-Al, which has satisfactory biosafety, is efficient in reducing neurotoxic effects and preventing neuronal tissue damage. |
format | Online Article Text |
id | pubmed-10539540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105395402023-09-30 Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection Xu, Weiqing Cai, Xiaoli Wu, Yu Wen, Yating Su, Rina Zhang, Yu Huang, Yuteng Zheng, Qihui Hu, Liuyong Cui, Xiaowen Zheng, Lirong Zhang, Shipeng Gu, Wenling Song, Weiyu Guo, Shaojun Zhu, Chengzhou Nat Commun Article Neurotoxicity of organophosphate compounds (OPs) can catastrophically cause nervous system injury by inhibiting acetylcholinesterase (AChE) expression. Although artificial systems have been developed for indirect neuroprotection, they are limited to dissociating P-O bonds for eliminating OPs. However, these systems have failed to overcome the deactivation of AChE. Herein, we report our finding that Al(3+) is engineered onto the nodes of metal–organic framework to synthesize MOF-808-Al with enhanced Lewis acidity. The resultant MOF-808-Al efficiently mimics the catalytic behavior of AChE and has a self-defense ability to break the activity inhibition by OPs. Mechanism investigations elucidate that Al(3+) Lewis acid sites with a strong polarization effect unite the highly electronegative –OH groups to form the enzyme-like catalytic center, resulting in superior substrate activation and nucleophilic attack ability with a 2.7-fold activity improvement. The multifunctional MOF-808-Al, which has satisfactory biosafety, is efficient in reducing neurotoxic effects and preventing neuronal tissue damage. Nature Publishing Group UK 2023-09-28 /pmc/articles/PMC10539540/ /pubmed/37770453 http://dx.doi.org/10.1038/s41467-023-41765-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Xu, Weiqing Cai, Xiaoli Wu, Yu Wen, Yating Su, Rina Zhang, Yu Huang, Yuteng Zheng, Qihui Hu, Liuyong Cui, Xiaowen Zheng, Lirong Zhang, Shipeng Gu, Wenling Song, Weiyu Guo, Shaojun Zhu, Chengzhou Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
title | Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
title_full | Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
title_fullStr | Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
title_full_unstemmed | Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
title_short | Biomimetic single Al-OH site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
title_sort | biomimetic single al-oh site with high acetylcholinesterase-like activity and self-defense ability for neuroprotection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539540/ https://www.ncbi.nlm.nih.gov/pubmed/37770453 http://dx.doi.org/10.1038/s41467-023-41765-x |
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