Mechanism-based inactivation of benzo(a)pyrene hydroxylase by aryl acetylenes and aryl olefins
Conference
·
· Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5322268
A series of aryl acetylenes and aryl olefins have been examined as substrates and inhibitors of cytochrome P-450 dependent monooxgenases in liver microsomes from 5,6-benzoflavone or phenobarbital pretreated rats. 1-Ethynylpyrene, 3-ethynylperylene, 2-ethynylfluorene, methyl 1-pyrenyl acetylene, cis- and trans-1-(2-bromovinyl)pyrene, and 1-allylpyrene serve as mechanism-based irreversible inactivators (suicide inhibitors) of benzo(a)pyrene hydroxylase, while 1-vinylpyrene and phenyl 1-pyrenyl acetylene do not cause a detectable suicide inhibition of benzo(a)pyrene hydroxylase. The mechanism-based loss of benzo(a)pyrene hydroxylase caused by the aryl acetylenes is not accompanied by a corresponding loss of the P-450 content of the microsomes (suicide destruction). The suicide inhibition by these aryl acetylenes therefore does not involve covalent binding to the heme moiety of the monooxygenase. Nevertheless, in the presence of NADPH, /sup 3/H-labeled 1-ethynylpyrene becomes covalently attached to the cytochrome P-450 protein; the measured stoichiometry of binding is one 1-ethynylpyrene per P-450 heme unit. The authors conclude that the inhibition of benzo(a)pyrene hydroxylase produced by 1-ethynylpyrene may be related to the mechanism of suicide inhibition of P-450 activity by chloramphenicol rather than the mechanism of suicide destruction of P-450 previously described for acetylene and propyne.
- Research Organization:
- Tulane Univ., New Orleans, LA
- OSTI ID:
- 5322268
- Report Number(s):
- CONF-8606151-
- Conference Information:
- Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 45:6
- Country of Publication:
- United States
- Language:
- English
Similar Records
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Thesis/Dissertation
·
Tue Dec 31 23:00:00 EST 1985
·
OSTI ID:6543960
1-Ethynylpyrene, a suicide inhibitor of cytochrome P-450 dependent benzo(a)pyrene hydroxylase activity in liver microsomes
Journal Article
·
Tue Aug 14 00:00:00 EDT 1984
· Biochemistry; (United States)
·
OSTI ID:5748563
Characterization and induction of aryl hydrocarbon (benzo(a)pyrene) hydroxylase in rabbit bone marrow
Journal Article
·
Fri Oct 01 00:00:00 EDT 1976
· Res. Commun. Chem. Pathol. Pharmacol.; (United States)
·
OSTI ID:7100338
Related Subjects
550201 -- Biochemistry-- Tracer Techniques
560301* -- Chemicals Metabolism & Toxicology-- Cells-- (-1987)
59 BASIC BIOLOGICAL SCIENCES
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ACETYLENE
ALKENES
ALKYNES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BIOLOGICAL EFFECTS
BODY
CELL CONSTITUENTS
COENZYMES
COVALENCE
DIGESTIVE SYSTEM
ENZYME ACTIVITY
ENZYMES
GLANDS
HYDROCARBONS
HYDROXYLASES
INHIBITION
KINETICS
LIVER
MAMMALS
MICROSOMES
NADP
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANOIDS
ORGANS
OXIDOREDUCTASES
PEPTIDES
PROTEINS
RATS
REACTION KINETICS
RODENTS
SUBSTRATES
VERTEBRATES
560301* -- Chemicals Metabolism & Toxicology-- Cells-- (-1987)
59 BASIC BIOLOGICAL SCIENCES
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ACETYLENE
ALKENES
ALKYNES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BIOLOGICAL EFFECTS
BODY
CELL CONSTITUENTS
COENZYMES
COVALENCE
DIGESTIVE SYSTEM
ENZYME ACTIVITY
ENZYMES
GLANDS
HYDROCARBONS
HYDROXYLASES
INHIBITION
KINETICS
LIVER
MAMMALS
MICROSOMES
NADP
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANOIDS
ORGANS
OXIDOREDUCTASES
PEPTIDES
PROTEINS
RATS
REACTION KINETICS
RODENTS
SUBSTRATES
VERTEBRATES