The major goal of this project is to determine the basic functional mechanism of cytochrome c oxidase (CcO), the terminal enzyme in the electron transfer chain. CcO is membrane-bound and has the dual function of reducing O2 to H2O to maintain electron flow to enable oxidative phosphorylation, and of coupling the oxygen reduction chemistry to proton translocation across the inner mitochondrial membrane, to generate a proton gradient. The enzyme plays an indispensable role in mammalian physiology because essentially all vital organs depend on aerobic metabolism. Despite years of intensive studies on CcO, the understanding of its catalytic processes is still incomplete and its mechanism of proton translocation remains unclear. We propose a variety of experiments to delineate the oxygen reduction chemistry and aim to shed new light on the coupled proton translocation. In order to identify the catalytic intermediates, new rapid mixing, laser photolysis and freeze trapping techniques will be applied to studies of both the mammalian and the bacterial forms of the enzyme. Full characterization will be done with resonance Raman scattering, optical absorption and electron paramagnetic resonance spectroscopies. One of the major focuses will be to determine the properties of the still controversial short-lived peroxo and ferryl intermediates. Resonance Raman and optical absorption spectroscopy will also be used in conjunction with a home-built continuous flow apparatus to monitor the time-dependent population of the reactive intermediates present during single as well as multiple turnover of the enzyme. To determine the role of specific residues in the functional processes of the enzyme, site directed mutants of CcO from bacteria will be expressed and analyzed by this multifaceted approach. In addition, the oxygen chemistry in a new class of model complexes, a mutant myoglobin with a binuclear center engineered in it to mimic the catalytic site of CcO, will be studied to elucidate the role of the binuclear heme-copper center. The energy transduction and proton translocation mechanism of CcO will be constructed, tested and refined.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM074982-04
Application #
7492991
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Fabian, Miles
Project Start
2005-09-03
Project End
2010-08-31
Budget Start
2008-09-01
Budget End
2010-08-31
Support Year
4
Fiscal Year
2008
Total Cost
$295,122
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Physiology
Type
Schools of Medicine
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Egawa, Tsuyoshi; Chen, Ying; Fee, James A et al. (2012) The rate-limiting step in O(2) reduction by cytochrome ba(3) from Thermus thermophilus. Biochim Biophys Acta 1817:666-71
Yu, Michelle A; Egawa, Tsuyoshi; Shinzawa-Itoh, Kyoko et al. (2012) Two tyrosyl radicals stabilize high oxidation states in cytochrome C oxidase for efficient energy conservation and proton translocation. J Am Chem Soc 134:4753-61
Lucas, M Fátima; Rousseau, Denis L; Guallar, Victor (2011) Electron transfer pathways in cytochrome c oxidase. Biochim Biophys Acta 1807:1305-13
Egawa, Tsuyoshi; Ganesan, Krithika; Lin, Myat T et al. (2011) Differential effects of glutamate-286 mutations in the aa(3)-type cytochrome c oxidase from Rhodobacter sphaeroides and the cytochrome bo(3) ubiquinol oxidase from Escherichia coli. Biochim Biophys Acta 1807:1342-8
Yu, Michelle A; Egawa, Tsuyoshi; Shinzawa-Itoh, Kyoko et al. (2011) Radical formation in cytochrome c oxidase. Biochim Biophys Acta 1807:1295-304
Yu, Michelle A; Egawa, Tsuyoshi; Yeh, Syun-Ru et al. (2010) EPR characterization of ascorbyl and sulfur dioxide anion radicals trapped during the reaction of bovine Cytochrome c Oxidase with molecular oxygen. J Magn Reson 203:213-9
Ji, Hong; Das, Tapan K; Puustinen, Anne et al. (2010) Modulation of the active site conformation by site-directed mutagenesis in cytochrome c oxidase from Paracoccus denitrificans. J Inorg Biochem 104:318-23
Sudhamsu, Jawahar; Kabir, Mariam; Airola, Michael V et al. (2010) Co-expression of ferrochelatase allows for complete heme incorporation into recombinant proteins produced in E. coli. Protein Expr Purif 73:78-82
Lu, Changyuan; Zhao, Xuan; Lu, Yi et al. (2010) Role of copper ion in regulating ligand binding in a myoglobin-based cytochrome C oxidase model. J Am Chem Soc 132:1598-605
Egawa, Tsuyoshi; Lee, Hyun Ju; Gennis, Robert B et al. (2009) Critical structural role of R481 in cytochrome c oxidase from Rhodobacter sphaeroides. Biochim Biophys Acta 1787:1272-5

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