We have used quartz crystal microbalance (QCM)-based real-time biospec
ific interaction measurement to analyze the binding of immunoliposomes
to antigen and examined the use of liposomes as signal-enhancing reag
ents in competitive QCM immunoassay. For the preparation of immunolipo
somes, various amounts of bacterially induced lipid-tagged single-chai
n antibody against 2-phenyloxazolone were incorporated in phosphatidyl
choline liposomes. The immunoliposomes bound specifically to immobiliz
ed hapten, and this binding was inhibited by soluble hapten in a conce
ntration-dependent manner. In this competitive assay, antigen could be
measured in the concentration range from 10(-5) to 10(-8) M.