AN ENZYME-LINKED-IMMUNOSORBENT-ASSAY METHOD TO MEASURE HUMAN APOLIPOPROTEIN-E LEVELS USING COMMERCIALLY AVAILABLE REAGENTS - EFFECT OF APOLIPOPROTEIN-E POLYMORPHISM ON SERUM APOLIPOPROTEIN-E CONCENTRATION
V. Gracia et al., AN ENZYME-LINKED-IMMUNOSORBENT-ASSAY METHOD TO MEASURE HUMAN APOLIPOPROTEIN-E LEVELS USING COMMERCIALLY AVAILABLE REAGENTS - EFFECT OF APOLIPOPROTEIN-E POLYMORPHISM ON SERUM APOLIPOPROTEIN-E CONCENTRATION, Analytical biochemistry, 223(2), 1994, pp. 212-217
A sensitive and specific enzyme-linked immunosorbent assay (ELISA) for
human apolipoprotein E (ape E) quantification using commercially avai
lable reagents is described. The assay is a noncompetitive, sandwich E
LISA in which the wells were coated with a monoclonal EO1 antibody ant
i-human ape E and detected with a polyclonal antibody-peroxidase conju
gate anti-apo E. The mean ape E concentration in 168 middle-aged subje
cts randomly selected from general population was 51.7 +/- 12.4 mg/lit
er. Apo E levels were highly correlated with ape E phenotypes. Apo E p
olymorphism, which shows a modulating effect in the catabolism of ape
E containing lipoproteins, may explain a large fraction, 18.5%, of the
variability of serum ape E levels in middle-aged population. Isoforms
apo E2 and apo E4 have an opposite effect on the regulation of serum
ape E concentrations. Individuals that express ape E2 isoform present
higher ape E levels (65.5 mg/liter for ape E2/E3), whereas the average
of individuals with ape E4 is lower (42.8 mg/liter for ape E4/E3) tha
n general population. (C) 1994 Academic Press, Inc.