In order to clarify the effects of the differences in physical states
of antigens on recognition by antibodies in immunoassays, the binding
characteristics of an antipeptide polyclonal antibody to the peptide a
nd the corresponding protein were studied. The reactivity in the immun
oliposome assay (ILA), as well as in the double-antibody sandwich ELIS
A, was identical to that in the solution. These results indicate that
the conformation of liposome-bound antigen is changed little by coupli
ng to liposomes and is almost the same as that of the native antigen i
n the liquid phase. It is desirable to assay by double-antibody sandwi
ch ELISA or ILA to detect native proteins, and the latter is very easi
ly performed.