The proposed research will develop an accessible, intuitive, and quantitative under- standing of proton-coupled electron transfer (PCET) processes. The primary focus is on processes in which a proton and an electron transfer in a single kinetic step but go to or come from distinct, separated sites. These multiple-site concerted proton-electron transfer (MS-CPET) reactions are widespread across biology but are not well understood. They are key to bioenergetics, central to the catalytic cycles of numerous metalloenzymes, and are involved in the chemistry of reactive oxygen species. MS-CPET is important in metabolism and bioactivation of many drugs, and defects in MS-CPET processes can lead to disease, for instance malfunctioning of the Q-cycle in complex III of the electron transport chain in mitochondria. The proposed studies will examine a range of small molecule systems to develop the fundamentals of MS-CPET and to model specific biochemical processes. The systems to be examined include phenols, iron porphyrins, ruthenium complexes, and models for iron/sulfur cluster cofactors. The phenol studies, for instance, will shed light on the formation of tyrosyl radicals in enzymatic catalysis or under oxidative stress. Using a broad range of model systems will provide insights that can be confidently transferred to more complex biological systems. Studies under specific aim 1 will build an intuition about these processes, for instance testing our hypothesis that separation of the electron and proton often does not inhibit the rate of reaction. Systematic variation of the e-/H+ separation and other relevant parameters will help develop quantitative models of how each parameter affects the MS-CPET reactions (specific aim 2). These studies will provide tests of current theory, and will explore how to simplify these theories to capture the larger effects and to be more accessible to experimentalists.
Specific aim 3 is to discover and understand the first examples of MS-CPET reactions involving C-H bonds, which could play an unappreciated role in biochemical processes. Together, the results from the different systems will build new intuition about MS-CPET and will provide the basis for new quantitative models. These will provide valuable understanding of a wide range of biological processes, and thus will be part of the foundation on which biomedical advances are built. The detailed knowledge available for electron transfer reactions has proven to be of great importance in biology. The work proposed aims to build a similarly valuable understanding for reactions that involve coupled transfers of electrons and protons.

Public Health Relevance

This project is developing a fundamental understanding of a class of chemical processes that occur widely in biology, the coupled transfers of electrons and protons. These chemical reactions are central to fields as diverse as bioenergetics and the action of antioxidants. Understanding these chemical processes is an important part of the foundation on which biomedical advances are being built.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM050422-17A1
Application #
8576361
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Anderson, Vernon
Project Start
1995-02-01
Project End
2017-06-30
Budget Start
2013-09-01
Budget End
2014-06-30
Support Year
17
Fiscal Year
2013
Total Cost
$304,357
Indirect Cost
$98,357
Name
University of Washington
Department
Type
Other Domestic Higher Education
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Porter, Thomas R; Hayes, Ellen C; Kaminsky, Werner et al. (2017) Sterically directed nitronate complexes of 2,6-di-tert-butyl-4-nitrophenoxide with Cu(ii) and Zn(ii) and their H-atom transfer reactivity. Dalton Trans 46:2551-2558
Bergner, Marie; Dechert, Sebastian; Demeshko, Serhiy et al. (2017) Model of the MitoNEET [2Fe-2S] Cluster Shows Proton Coupled Electron Transfer. J Am Chem Soc 139:701-707
Wang, Yu-Heng; Pegis, Michael L; Mayer, James M et al. (2017) Molecular Cobalt Catalysts for O2 Reduction: Low-Overpotential Production of H2O2 and Comparison with Iron-Based Catalysts. J Am Chem Soc 139:16458-16461
Kolmar, Scott S; Mayer, James M (2017) SmI2(H2O)n Reduction of Electron Rich Enamines by Proton-Coupled Electron Transfer. J Am Chem Soc 139:10687-10692
Kim, Byoungmoo; Storch, Golo; Banerjee, Gourab et al. (2017) Stereodynamic Quinone-Hydroquinone Molecules That Enantiomerize at sp3-Carbon via Redox-Interconversion. J Am Chem Soc 139:15239-15244
Cattaneo, Mauricio; Ryken, Scott A; Mayer, James M (2017) Outer-Sphere 2?e- /2?H+ Transfer Reactions of Ruthenium(II)-Amine and Ruthenium(IV)-Amido Complexes. Angew Chem Int Ed Engl 56:3675-3678
Morris, Wesley D; Mayer, James M (2017) Separating Proton and Electron Transfer Effects in Three-Component Concerted Proton-Coupled Electron Transfer Reactions. J Am Chem Soc 139:10312-10319
Porter, Thomas R; Capitao, Dany; Kaminsky, Werner et al. (2016) Synthesis, Radical Reactivity, and Thermochemistry of Monomeric Cu(II) Alkoxide Complexes Relevant to Cu/Radical Alcohol Oxidation Catalysis. Inorg Chem 55:5467-75
Hayes, Ellen C; Porter, Thomas R; Barrows, Charles J et al. (2016) Electronic Structure of a Cu(II)-Alkoxide Complex Modeling Intermediates in Copper-Catalyzed Alcohol Oxidations. J Am Chem Soc 138:4132-45

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