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.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11282276 | PMC |
http://dx.doi.org/10.1038/s41467-024-50687-1 | DOI Listing |
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