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PMID: 3410841 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Thiol/disulfide exchange between 3-hydroxy-3-methylglutaryl-CoA reductase and glutathione. A thermodynamically facile dithiol oxidation.

The Journal of biological chemistry ·Vol. 263 ·No. 25 ·1988-09-05 ·Pages 12204-12

Cappel RE, Gilbert HF

Abstract

In glutathione redox buffers, rat liver, microsomal 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase rapidly equilibrates between a reduced, active form and an oxidized, inactive form. At pH 7.0, 37 degrees C, the second order rate constant for inactivation of the reduced enzyme by GSSG is 1700 +/- 200 M-1 min-1, approximately 20-fold faster than the reaction of GSSG with a typical, unhindered thiol of pKa 7.7. High concentrations of GSH or lower concentrations of dithiothreitol restore the activity of the oxidized enzyme. The oxidation of the enzyme by GSSG is only 30-fold slower in the presence of saturating levels of both substrates. The incomplete inhibition of thiol/disulfide exchange by substrates can lead to significant changes in the activity of the enzyme during the assay when glutathione is present. At redox equilibrium, both in the absence and presence of substrates, the activity of the enzyme depends on the quantity [GSH]2/[GSSG], suggesting that the redox transition involves the formation of a protein-SS-protein disulfide. The equilibrium constant for the reaction HMGRred + GSSG in equilibrium HMGRox + 2 GSH is 0.55 +/- 0.07 M in the absence of substrates and 0.20 +/- 0.02 M in the presence of saturating levels of both substrates. Thus, HMG-CoA reductase is very sensitive to dithiol oxidation both kinetically and thermodynamically. Significant changes in the oxidation state and activity of this enzyme could be expected to result from normal changes in the thiol/disulfide oxidation state of the cellular glutathione redox buffer.

MeSH Terms
Animals Disulfides/metabolism Dithiothreitol/pharmacology Enzyme Activation/drug effects Enzyme Reactivators Glutathione/metabolism,pharmacology Hydroxymethylglutaryl CoA Reductases/metabolism Hydroxymethylglutaryl-CoA Reductase Inhibitors Kinetics Male Microsomes, Liver/enzymology Oxidation-Reduction Rats Rats, Inbred Strains Sulfhydryl Compounds/metabolism Thermodynamics
Chemicals
Disulfides Enzyme Reactivators Hydroxymethylglutaryl-CoA Reductase Inhibitors Sulfhydryl Compounds Hydroxymethylglutaryl CoA Reductases Glutathione Dithiothreitol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cappel R E
Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030.
Gilbert H F
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1988-09-05
Pages
12204-12
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL-01020 · United States
NHLBI NIH HHS · HL-28521 · United States
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