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Journal of Lipid Research, Vol 25, 1159-1166, Copyright © 1984 by Lipid Research, Inc.
B Angelin, K Einarsson, L Liljeqvist, K Nilsell and RA Heller
3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, the enzyme
catalyzing the rate-limiting step in cholesterol biosynthesis, exists in
one active (dephosphorylated) and one inactive (phosphorylated) form in
liver microsomes obtained from several animal species. The present study
was undertaken in order to determine a) whether the human enzyme also
exists in active and inactive readily interconvertible forms; b) whether
the large inter-individual variation in HMG-CoA reductase activity observed
in normal man can be explained by variations in the activation state of the
enzyme; and c) to characterize the reactivity of antibodies raised against
rat liver HMG-CoA reductase with the intact human microsomal enzyme.
HMG-CoA reductase activity, assayed in microsomes prepared in the presence
of 50 mM NaF, was only 17 +/- 3% of the activity observed in microsomes
prepared from the same liver in the absence of fluoride. Preincubation of
microsomes prepared in NaF with alkaline phosphatase resulted in a tenfold
increase of enzyme activity, while the activity of microsomes prepared
without fluoride was increased also (by about 45%) with this treatment. On
the other hand, the activated enzyme could be inactivated by incubation of
microsomes with Mg-ATP. In eleven normal weight, normolipidemic gallstone
patients, the HMG-CoA reductase activity determined in microsomes prepared
without NaF ("standard procedure") reflected well both the "expressed"
activity (in microsomes prepared with NaF) and the "total" (fully
activated) enzyme activity; correlation coefficients were +0.80 and +0.84,
respectively. Preincubation of human liver microsomes with rabbit antiserum
against partially purified HMG-CoA reductase from rat liver resulted in a
72 +/- 6% inhibition of enzyme activity.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
3-hydroxy-3-methylglutaryl coenzyme A reductase in human liver microsomes: active and inactive forms and cross-reactivity with antibody against rat liver enzyme
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