The overall goal of the research is to elucidate the mechanisms of action of enzymes that catalyze oxidations of hydrocarbons and amines. The former group includes the heme-thiolate cytochrome P450 enzymes and diiron enzymes such as methane monooxygenase and stearoyl desaturase. The latter group includes the monoamine oxidase (MAO) enzymes as well as P450 enzymes. An understanding of the mechanisms of actions of these enzymes is expected to be beneficial for therapeutic advances, for example, MAO is the target enzyme of drugs for treatment of depression and Parkinson's Disease. The method of study involves the use of """"""""hypersensitive"""""""" radical probes that can be employed as substrates in oxidations to reveal the intermediacy of very short-lived radicals. The probe substrates are designed, and the radical reaction rate constants are determined. From product distributions in enzyme oxidations, the intermediacy of a radical is determined, and, if a radical is an intermediate, the lifetime of the radical is measured. For studies of hydrocarbon oxidations by iron-containing enzymes, some hypersensitive probes now exist, and the development of other probes is planned. Especially noteworthy is a family of probes that distinguish between radical and cationic intermediates while maintaining hypersensitive reactivity in the radical reaction. Enzyme catalyzed oxidations of calibrated probes are in progress in the PI's laboratory, using enzymes purified by other groups, and in the laboratories of other groups, using probes supplied by the PI's group. The results are expected to delineate common and dissimilar features in the mechanisms of reactions of the seemingly distinct enzymes. For studies of enzyme catalyzed amine oxidations, the work is at a more fundamental stage. Kinetic scales for reactions of a wide range of nitrogen containing radicals are being measured by a combination of direct, laser flash photolysis methods and indirect kinetic competition techniques. When the reactions of the nitrogen containing radicals are understood, rationally designed mechanistic probes will be developed and applied in oxidation reactions by P450 and MAO enzymes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM048722-07
Application #
2900797
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1993-01-01
Project End
2001-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Wayne State University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
City
Detroit
State
MI
Country
United States
Zip Code
48202
Zhang, Rui; Vanover, Eric; Luo, Weilong et al. (2014) Photochemical generation and kinetic studies of a putative porphyrin-ruthenium(V)-oxo species. Dalton Trans 43:8749-56
Su, Zhi; Horner, John H; Newcomb, Martin (2012) Cytochrome P450 119 Compounds?I Formed by Chemical Oxidation and Photooxidation Are the Same Species. Chemistry :
Su, Zhi; Horner, John H; Newcomb, Martin (2012) Rates of fatty acid oxidations by P450 compound I are pH dependent. Chembiochem 13:2061-4
Pan, Zhengzheng; Newcomb, Martin (2011) Acid-catalyzed disproportionation of oxoiron(IV) porphyrins to give oxoiron(IV) porphyrin radical cations. Inorg Chem Commun 14:968-970
Chen, Xiaohong; Su, Zhi; Horner, John H et al. (2011) Oxidation of 10-undecenoic acid by cytochrome P450(BM-3) and its Compound I transient. Org Biomol Chem 9:7427-33
Yuan, Xinting; Sheng, Xin; Horner, John H et al. (2010) Low temperature photo-oxidation of chloroperoxidase Compound II. J Inorg Biochem 104:1156-63
Vanover, Eric; Huang, Yan; Xu, Libin et al. (2010) Photocatalytic aerobic oxidation by a bis-porphyrin-ruthenium(IV) mu-oxo dimer: observation of a putative porphyrin-ruthenium(V)-oxo intermediate. Org Lett 12:2246-9
Harischandra, Dilusha N; Lowery, Gerald; Zhang, Rui et al. (2009) Production of a putative iron(V)-oxocorrole species by photo-disproportionation of a bis-corrole-diiron(IV)-mu-oxo dimer: implication for a green oxidation catalyst. Org Lett 11:2089-92
Yuan, Xinting; Wang, Qin; Horner, John H et al. (2009) Kinetics and activation parameters for oxidations of styrene by Compounds I from the cytochrome P450(BM-3) (CYP102A1) heme domain and from CYP119. Biochemistry 48:9140-6
Pan, Zhengzheng; Wang, Qin; Sheng, Xin et al. (2009) Highly reactive porphyrin-iron-oxo derivatives produced by photolyses of metastable porphyrin-iron(IV) diperchlorates. J Am Chem Soc 131:2621-8

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