Synthetic peptides are covalently linked to immunogenic carrier proteins to
enhance the anti-peptide immune response. To investigate whether the metho
d of conjugation influences the immune response, we evaluated two distinctl
y different choices of linker for a peptide-carrier construct. HPG-30, a sy
nthetic peptide derived from the p17 gag protein of human immunodeficiency
virus 1, was covalently linked to keyhole limper hemocyanin by either gluta
raldehyde or a maleimide ester. Glutaraldehyde linkage enhanced tile anti-p
eptide antibody and native protein response compared to maleimide. The male
imide-linked conjugate was more effective at inducing a peptide-specific ce
llular response. Thus, manipulation of the conjugation method can modify th
e magnitude and character of the immune response to a synthetic peptide vac
cine.