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Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening

A biomimetic mineralization method was used in the facile and rapid preparation of nanoflowers for immobilizing alcohol dehydrogenase (ADH). The method mainly uses ADH as an organic component and zinc phosphate as an inorganic component to prepare flower-like ADH/Zn(3)(PO(4))(2) organic-inorganic hy...

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Autores principales: Luo, Mao-Ling, Chen, Hua, Chen, Guo-Ying, Wang, Shengpeng, Wang, Yitao, Yang, Feng-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386709/
https://www.ncbi.nlm.nih.gov/pubmed/37513303
http://dx.doi.org/10.3390/molecules28145429
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author Luo, Mao-Ling
Chen, Hua
Chen, Guo-Ying
Wang, Shengpeng
Wang, Yitao
Yang, Feng-Qing
author_facet Luo, Mao-Ling
Chen, Hua
Chen, Guo-Ying
Wang, Shengpeng
Wang, Yitao
Yang, Feng-Qing
author_sort Luo, Mao-Ling
collection PubMed
description A biomimetic mineralization method was used in the facile and rapid preparation of nanoflowers for immobilizing alcohol dehydrogenase (ADH). The method mainly uses ADH as an organic component and zinc phosphate as an inorganic component to prepare flower-like ADH/Zn(3)(PO(4))(2) organic-inorganic hybrid nanoflowers (HNFs) with the high specific surface area through a self-assembly process. The synthesis conditions of the ADH HNFs were optimized and its morphology was characterized. Under the optimum enzymatic reaction conditions, the Michaelis-Menten constant (K(m)) of ADH HNFs (β-NAD(+) as substrate) was measured to be 3.54 mM, and the half-maximal inhibitory concentration (IC(50)) of the positive control ranitidine (0.2–0.8 mM) was determined to be 0.49 mM. Subsequently, the inhibitory activity of natural medicine Penthorum chinense Pursh and nine small-molecule compounds on ADH was evaluated using ADH HNFs. The inhibition percentage of the aqueous extract of P. chinense is 57.9%. The vanillic acid, protocatechuic acid, gallic acid, and naringenin have obvious inhibitory effects on ADH, and their percentages of inhibition are 55.1%, 68.3%, 61.9%, and 75.5%, respectively. Moreover, molecular docking analysis was applied to explore the binding modes and sites of the four most active small-molecule compounds to ADH. The results of this study can broaden the application of immobilized enzymes through biomimetic mineralization, and provide a reference for the discovery of ADH inhibitors from natural products.
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spelling pubmed-103867092023-07-30 Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening Luo, Mao-Ling Chen, Hua Chen, Guo-Ying Wang, Shengpeng Wang, Yitao Yang, Feng-Qing Molecules Article A biomimetic mineralization method was used in the facile and rapid preparation of nanoflowers for immobilizing alcohol dehydrogenase (ADH). The method mainly uses ADH as an organic component and zinc phosphate as an inorganic component to prepare flower-like ADH/Zn(3)(PO(4))(2) organic-inorganic hybrid nanoflowers (HNFs) with the high specific surface area through a self-assembly process. The synthesis conditions of the ADH HNFs were optimized and its morphology was characterized. Under the optimum enzymatic reaction conditions, the Michaelis-Menten constant (K(m)) of ADH HNFs (β-NAD(+) as substrate) was measured to be 3.54 mM, and the half-maximal inhibitory concentration (IC(50)) of the positive control ranitidine (0.2–0.8 mM) was determined to be 0.49 mM. Subsequently, the inhibitory activity of natural medicine Penthorum chinense Pursh and nine small-molecule compounds on ADH was evaluated using ADH HNFs. The inhibition percentage of the aqueous extract of P. chinense is 57.9%. The vanillic acid, protocatechuic acid, gallic acid, and naringenin have obvious inhibitory effects on ADH, and their percentages of inhibition are 55.1%, 68.3%, 61.9%, and 75.5%, respectively. Moreover, molecular docking analysis was applied to explore the binding modes and sites of the four most active small-molecule compounds to ADH. The results of this study can broaden the application of immobilized enzymes through biomimetic mineralization, and provide a reference for the discovery of ADH inhibitors from natural products. MDPI 2023-07-15 /pmc/articles/PMC10386709/ /pubmed/37513303 http://dx.doi.org/10.3390/molecules28145429 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Luo, Mao-Ling
Chen, Hua
Chen, Guo-Ying
Wang, Shengpeng
Wang, Yitao
Yang, Feng-Qing
Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening
title Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening
title_full Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening
title_fullStr Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening
title_full_unstemmed Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening
title_short Preparation of Alcohol Dehydrogenase–Zinc Phosphate Hybrid Nanoflowers through Biomimetic Mineralization and Its Application in the Inhibitor Screening
title_sort preparation of alcohol dehydrogenase–zinc phosphate hybrid nanoflowers through biomimetic mineralization and its application in the inhibitor screening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386709/
https://www.ncbi.nlm.nih.gov/pubmed/37513303
http://dx.doi.org/10.3390/molecules28145429
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