The aim of this study was to investigate the molecular basis of human IgE-a
llergen interaction by screening a phage-displayed peptide library with an
allergen-specific human IgE-mimicking monoclonal antibody (mAb). A mAb that
reacted with major grass pollen allergens was successfully identified and
shown to inhibit human IgE-allergen interaction. Biopanning of a phage-disp
layed random peptide library with this mAb yielded a 12 amino acid long mim
otope. A synthetic peptide based on this 12-mer mimotope inhibited mAb and
human IgE binding to grass pollen extracts. Our results indicate that such
synthetic peptide mimotopes of allergens have potential as novel therapeuti
c agents. (C) 2001 Published by Elsevier Science B.V.. on behalf of the Fed
eration of European Biochemical Societies.