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In vitro inactivation of mammalian methionine synthase by nitric oxide
Author(s) -
NICOLAOU A.,
KENYON S. H.,
GIBBONS J. M.,
AST T.,
Gibbons W. A.
Publication year - 1996
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1046/j.1365-2362.1996.122254.x
Subject(s) - nitric oxide synthase , in vitro , methionine , methionine synthase , chemistry , nitric oxide , biochemistry , enzyme , amino acid , organic chemistry
The research described here provides one mechanism of uniting current effects of nitric oxide (NO) with the elevated levels of homocysteine detected in patients with cardiovascular and other disease. Time‐ and dose‐dependent studies of the inhibition of purified mammalian methionine synthase by NO were performed. The in vitro study gave an effective IC 50 value of 3 μmol L ‐1 . Methionine synthase converts cellular homocysteine to methionine and is a major enzyme in the biosynthetic pathways for folates, S ‐adenosylmethionine and biological methylations, sulphur amino acids and polyamines. Nitric oxide‐induced inactivation of methionine synthase alters the levels of these metabolites and could therefore provide a connection between the cardiovascular effects of NO, the plasma homo‐cysteine levels and cardiovascular diseases that is complementary to the more traditional NO‐induced stimulation of guanylate cyclase and the convertion of homocysteine to oxidized sulphur amino acids.