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构建高效人工酶的氧化还原位点和路易斯酸的仿生协同效应。

Biomimetic synergistic effect of redox site and Lewis acid for construction of efficient artificial enzyme.

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan, 250014, P. R. China.

Jinan Institute of Quantum Technology, Jinan, 250101, P. R. China.

出版信息

Nat Commun. 2024 Jul 26;15(1):6315. doi: 10.1038/s41467-024-50687-1.

Abstract

In enzymatic catalysis, the redox site and Lewis acid are the two main roles played by metal to assist amino acids. However, the reported enzyme mimics only focus on the redox-active metal as redox site, while the redox-inert metal as Lewis acid has, to the best of our knowledge, not been studied, presenting a bottleneck of enzyme mimics construction. Based on this, a series of highly efficient MVO·nHO peroxidase mimics with vanadium as redox site and alkaline-earth metal ion (M) as Lewis acid are reported. Experimental results and theoretical calculations indicate the peroxidase-mimicking activity of MVO·nHO show a periodic change with the Lewis acidity (ion potential) of M, revealing the mechanism of redox-inert M regulating electron transfer of V-O through non-covalent polarization and thus promoting HO adsorbate dissociation. The biomimetic synergetic effect of redox site and Lewis acid is expected to provide an inspiration for design of enzyme mimics.

摘要

在酶催化中,金属起到辅助氨基酸的两个主要作用,分别是氧化还原位点和路易斯酸。然而,据我们所知,目前报道的酶模拟物仅关注氧化还原活性金属作为氧化还原位点,而氧化还原惰性金属作为路易斯酸尚未被研究,这成为了酶模拟物构建的一个瓶颈。基于此,本文报道了一系列以钒作为氧化还原位点、碱土金属离子(M)作为路易斯酸的高效 MVOnHO 过氧化物酶模拟物。实验结果和理论计算表明,MVO·nHO 的过氧化物酶模拟活性随 M 的路易斯酸度(离子势)呈现周期性变化,揭示了氧化还原惰性 M 通过非共价极化调节 V-O 电子转移从而促进 HO 吸附物解离的机制。氧化还原位点和路易斯酸的仿生协同效应有望为酶模拟物的设计提供启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94a4/11282276/40cfac9dc2d1/41467_2024_50687_Fig1_HTML.jpg

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