Cu (along with Fe) enzymes play dominant roles in O2 activation in Nature. They are important in melanogenesis, neurochemistry, metal ion metabolism, proton pumping, bioremediation, ROS generation, a range of disease states, and can be utilized in biofuel cells for implantable devices. On a molecular level these can reduce O2 by 1,2, possibly 3 and 4 electrons to accomplish a range of functions, including H-atom abstraction from both weak and strong C-H bonds, electrophilic activation by 2 as well as 1 Cu center, and the coupling of O2 reduction to water to Fe metabolism by the multicopper oxidases and proton pumping by the heme-copper oxidases. Oxygen- activating Cu enzymes are divided into five classes based on structure and type of reaction with the mononuclear Cu class further divided based on the redox active states of the Cu and the oxygen. Our studies use the combination of kinetics on the enzymes to obtain intermediates, application of a wide range of spectroscopies to define these, parallel model studies and the coupling of the results of these kinetic, spectroscopic and model studies to electronic structure calculations to define frontier molecular orbitals and reaction coordinates in catalysis. Innovative aspects of this research effort include the development of new spectroscopic methods, the analyses of the unique spectral features often exhibited by Cu/O2 intermediates in terms of their geometric and electronic structures and the coupling of these data to electronic structure calculations for development of experimentally validated reaction coordinates. These studies define the reaction mechanisms of each class and subclass on a molecular level (important in the design of drugs, devices and catalysts) and by parallel studies over the classes develop general insight into structure/function correlations over oxygen utilization in Nature.

Public Health Relevance

O2 activating copper enzymes are important in the biosynthesis of natural products,1 melanins,2 hormones and neurotransmitters;3-6 proton pumping for ATP synthesis;7-9 iron metabolism;10-12; the generation of reactive oxygen species (ROS) in neurodegenerative diseases;13,14 biosensors and biofuel cells for implantable devices;15,16 and are related to a number of human diseases (Parkinson's,17-19 aceruloplasminemia,10,11,20 oculocutaneous albinism,21-23 a range of cancers24-27, etc.). Understanding their reactivity and control of function on a molecular level contributes to human health and biotechnology by enabling rational drug, catalyst and device development and uncovering the molecular bases of disease states.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK031450-40
Application #
9953871
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Sechi, Salvatore
Project Start
1982-01-01
Project End
2024-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
40
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Stanford University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Sharma, Savita K; Schaefer, Andrew W; Lim, Hyeongtaek et al. (2017) A Six-Coordinate Peroxynitrite Low-Spin Iron(III) Porphyrinate Complex-The Product of the Reaction of Nitrogen Monoxide (·NO(g)) with a Ferric-Superoxide Species. J Am Chem Soc 139:17421-17430
Schaefer, Andrew W; Kieber-Emmons, Matthew T; Adam, Suzanne M et al. (2017) Phenol-Induced O-O Bond Cleavage in a Low-Spin Heme-Peroxo-Copper Complex: Implications for O2 Reduction in Heme-Copper Oxidases. J Am Chem Soc 139:7958-7973
Garcia-Bosch, Isaac; Cowley, Ryan E; Díaz, Daniel E et al. (2016) Dioxygen Activation by a Macrocyclic Copper Complex Leads to a Cu2O2 Core with Unexpected Structure and Reactivity. Chemistry 22:5133-7

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