Phage library clones selected by a conformational epitope-recognizing
and inhibitory monoclonal antibody may display moieties that mimic a r
eceptor/ligand-like three-dimensional structure. This pseudoreceptor/l
igand should be able to bind to natural ligand/receptor molecules. We
tested this idea using anti-T cell costimulatory molecule antibodies a
nd successfully isolated phage clones with costimulatory effects on T-
cell proliferation, This strategy facilitates the designing of regulat
ory peptide molecules in the absence of precise information about the
structure-function relationships in receptor/ligand interactions.