Dopamine Beta-monooxygenase catalyzes the final step in the biosynthesis of norepinephrine from tyrosine. Norepinephrine serves either as a hormone (in the adrenal gland) or a neurotransmitter (in the sympathetic nervous system); it is also a precursor in epinephrine biosynthesis in the adrenal gland. Because of the vital physiologic roles played by norepinephrine, dopamine Beta-monooxygenase is a logical target in establishing a molecular basis for our understanding of neurologic disorders and in developing drug therapies. The goals of this proposal are to determine the molecular mechanisms of dopamine Beta-monooxygenase catalysis and regulation for enzyme from bovine adrenal gland. Steady-state isotope and substituent effects will be investigated to establish the order of addition of reducing equivalents to enzyme, the nature of the E.P complex, and the mode of C-H bond activation. The nature of binding of two coppers per subunit will be investigated, as will the participation of these coppers in substrate/oxygen activation. The catalytic role of copper will be addressed by rapid freeze-quench kinetic studies, to follow the pre-steady state time course for E-Cu(II) reduction by ascorbate and reoxidation by dopamine and oxygen. These studies, together with proposed rapid acid-quench kinetics to monitor the formation of enzyme-bound norepinephrine, should allow us to distinguish among postulated chemical mechanisms. The mechanism of suicide inhibition by Beta-chlorophenethylamine and phenacetaldehyde derivatives will pursued, as probes for the nature of reactive intermediates in enzyme inactivation. Such studies may lead to therapeutic agents, via the specific inactivation of dopamine Beta-monooxygenase. Finally, the properties of dopamine Beta-monooxygenase in chromaffin vesicle ghosts will be studied, with the long-range goal of establishing the extent to which ATPase, the catecholamine carrier, dopamine Beta-monooxygenase, and electron transport proteins influence norepinephrine production in this multi-protein system.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM025765-08
Application #
3273289
Study Section
Biochemistry Study Section (BIO)
Project Start
1978-06-01
Project End
1990-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
8
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Horitani, Masaki; Offenbacher, Adam R; Carr, Cody A Marcus et al. (2017) 13C ENDOR Spectroscopy of Lipoxygenase-Substrate Complexes Reveals the Structural Basis for C-H Activation by Tunneling. J Am Chem Soc 139:1984-1997
Collazo, Lara; Klinman, Judith P (2016) Control of the Position of Oxygen Delivery in Soybean Lipoxygenase-1 by Amino Acid Side Chains within a Gas Migration Channel. J Biol Chem 291:9052-9
Zhang, Jianyu; Klinman, Judith P (2016) Convergent Mechanistic Features between the Structurally Diverse N- and O-Methyltransferases: Glycine N-Methyltransferase and Catechol O-Methyltransferase. J Am Chem Soc 138:9158-65
Hu, Shenshen; Cattin-Ortolá, Jérôme; Munos, Jeffrey W et al. (2016) Hydrostatic Pressure Studies Distinguish Global from Local Protein Motions in C-H Activation by Soybean Lipoxygenase-1. Angew Chem Int Ed Engl 55:9361-4
Latham, John A; Iavarone, Anthony T; Barr, Ian et al. (2015) PqqD is a novel peptide chaperone that forms a ternary complex with the radical S-adenosylmethionine protein PqqE in the pyrroloquinoline quinone biosynthetic pathway. J Biol Chem 290:12908-18
Zhang, Jianyu; Kulik, Heather J; Martinez, Todd J et al. (2015) Mediation of donor-acceptor distance in an enzymatic methyl transfer reaction. Proc Natl Acad Sci U S A 112:7954-9
Zhang, Jianyu; Klinman, Judith P (2015) High-performance liquid chromatography separation of the (S,S)- and (R,S)-forms of S-adenosyl-L-methionine. Anal Biochem 476:81-3
Zhu, Hui; Peck, Spencer C; Bonnot, Florence et al. (2015) Oxygen-18 Kinetic Isotope Effects of Nonheme Iron Enzymes HEPD and MPnS Support Iron(III) Superoxide as the Hydrogen Abstraction Species. J Am Chem Soc 137:10448-51
Sharma, Sudhir C; Klinman, Judith P (2015) Kinetic Detection of Orthogonal Protein and Chemical Coordinates in Enzyme Catalysis: Double Mutants of Soybean Lipoxygenase. Biochemistry 54:5447-56
Zhu, Hui; Sommerhalter, Monika; Nguy, Andy K L et al. (2015) Solvent and Temperature Probes of the Long-Range Electron-Transfer Step in Tyramine ?-Monooxygenase: Demonstration of a Long-Range Proton-Coupled Electron-Transfer Mechanism. J Am Chem Soc 137:5720-9

Showing the most recent 10 out of 92 publications