Albumin microspheres (AMS), of which the average diameter is 240 +/- 10 nm, were prepared by pH control and heat treatment. Cytochrome c and rGPIb alpha; a water-soluble fragment of the alpha chain of a recombinant platelet glycoprotein (GP)Ib containing a von Willebrand factor (vWf)-binding site were selected as a receptor protein. Cytochrome c was used as a probe protein for monitoring. Onto the surface of the AMS and those proteins, N-succinimidyl 3-(2-pyridyldithio)propionate (SPDP) was reacted through the amide linkage to obtain PD-AMS, PD-cytochrome c, and PD-rGPIb alpha, respectively. The latter two were further reduced to SH-cytochrome c and SH-rGPIb alpha by dithiothreitol and conjugated with PD-AMS by a thiol-disulfide exchange reaction. The resulting AMS contain cytochrome c or rGPIb alpha of about 25000 or 2500 molecules, respectively. The addition of ristocetin to the rGPIb alpha -AMS in the presence of vWf caused specific aggregation. Furthermore, the rGPIb alpha -AMS enhanced the ristocetin induced platelet aggregation in a low platelet concentration (4.0 x 10(7)/mL).