Issue 43, 2019

Electric field modulated redox-driven protonation and hydration energetics in energy converting enzymes

Abstract

Biological energy conversion is catalysed by proton-coupled electron transfer (PCET) reactions that form the chemical basis of respiratory and photosynthetic enzymes. Despite recent advances in structural, biophysical, and computational experiments, the mechanistic principles of these reactions still remain elusive. Based on common functional features observed in redox enzymes, we study here generic mechanistic models for water-mediated long-range PCET reactions. We show how a redox reaction within a buried protein environment creates an electric field that induces hydration changes between the proton acceptor and donor groups, and in turn, lowers the reaction barrier and increases the thermodynamic driving forces for the water-mediated PCET process. We predict linear free energy relationships, and discuss the proposed mechanism in context of PCET in cytochrome c oxidase.

Graphical abstract: Electric field modulated redox-driven protonation and hydration energetics in energy converting enzymes

Supplementary files

Article information

Article type
Communication
Submitted
08 fev 2019
Accepted
01 abr 2019
First published
08 mai 2019
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2019,55, 6078-6081

Electric field modulated redox-driven protonation and hydration energetics in energy converting enzymes

P. Saura, D. M. Frey, A. P. Gamiz-Hernandez and V. R. I. Kaila, Chem. Commun., 2019, 55, 6078 DOI: 10.1039/C9CC01135H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements