| Literature DB >> 28221360 |
Ambika Bhagi-Damodaran1, Matthew A Michael2, Qianhong Zhu3, Julian Reed4, Braddock A Sandoval1, Evan N Mirts5, Saumen Chakraborty1, Pierre Moënne-Loccoz3, Yong Zhang2, Yi Lu1,4,5.
Abstract
Haem-copper oxidase (HCO) catalyses the natural reduction of oxygen to water using a haem-copper centre. Despite decades of research on HCOs, the role of non-haem metal and the reason for nature's choice of copper over other metals such as iron remains unclear. Here, we use a biosynthetic model of HCO in myoglobin that selectively binds different non-haem metals to demonstrate 30-fold and 11-fold enhancements in the oxidase activity of Cu- and Fe-bound HCO mimics, respectively, as compared with Zn-bound mimics. Detailed electrochemical, kinetic and vibrational spectroscopic studies, in tandem with theoretical density functional theory calculations, demonstrate that the non-haem metal not only donates electrons to oxygen but also activates it for efficient O-O bond cleavage. Furthermore, the higher redox potential of copper and the enhanced weakening of the O-O bond from the higher electron density in the d orbital of copper are central to its higher oxidase activity over iron. This work resolves a long-standing question in bioenergetics, and renders a chemical-biological basis for the design of future oxygen-reduction catalysts.Entities:
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Year: 2016 PMID: 28221360 PMCID: PMC5321616 DOI: 10.1038/nchem.2643
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427