期刊
FRONTIERS IN CHEMISTRY
卷 9, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2021.640155
关键词
cytochrome c oxidase; energy conservation; proton pumping; redox-active tyrosine; midpoint potentials; density functional theory
资金
- Swedish Research Council [2018-05973, 2016-03721]
- Swedish Research Council [2016-03721] Funding Source: Swedish Research Council
- Vinnova [2016-03721] Funding Source: Vinnova
Cellular respiration involves electron transport via enzyme complexes to terminal Cytochrome c oxidase, where molecular oxygen is reduced to water, establishing a transmembrane electrochemical gradient using the free energy released. The redox-active tyrosine in CcOs plays a crucial role in energy conservation by allowing proton pumping in all reduction steps. The unprotonated tyrosine provides a mechanism for coupling the uptake of two protons per electron in every reduction step, ensuring secure proton pumping.
Cellular respiration involves electron transport via a number of enzyme complexes to the terminal Cytochrome c oxidase (CcO), in which molecular oxygen is reduced to water. The free energy released in the reduction process is used to establish a transmembrane electrochemical gradient, via two processes, both corresponding to charge transport across the membrane in which the enzymes are embedded. First, the reduction chemistry occurring in the active site of CcO is electrogenic, which means that the electrons and protons are delivered from opposite sides of the membrane. Second, the exergonic chemistry is coupled to translocation of protons across the entire membrane, referred to as proton pumping. In the largest subfamily of the CcO enzymes, the A-family, one proton is pumped for every electron needed for the chemistry, making the energy conservation particularly efficient. In the present study, hybrid density functional calculations are performed on a model of the A-family CcOs. The calculations show that the redox-active tyrosine, conserved in all types of CcOs, plays an essential role for the energy conservation. Based on the calculations a reaction mechanism is suggested involving a tyrosyl radical (possibly mixed with tyrosinate character) in all reduction steps. The result is that the free energy released in each reduction step is large enough to allow proton pumping in all reduction steps without prohibitively high barriers when the gradient is present. Furthermore, the unprotonated tyrosine provides a mechanism for coupling the uptake of two protons per electron in every reduction step, i.e. for a secure proton pumping.
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