Immunoreactive, multicomponent nanoclusters were assembled through the controlled presentation of a known, synthetic peptide epitope. The epitope comes from the hemagglutanin protein of influenza and is known to bind to a monoclonal anti-HA antibody. Antibody affinity for the immunoreactive MPC was compared to the affinity for traditionally used peptide arrays using the quartz crystal microbalance. The two systems had comparable affinities (K-a), ranging from 0.41 x 10(7) M-1 to 1.8 x 10(7) M-1, though the nanocluster used a much lower density of peptide relative to that of the peptide array. These results suggest that functionalized nanoclusters have potential in nanostructure assembly and medical applications. Water-soluble nanoparticles that present known neutralizing peptide epitopes of protein antigens might be used in antiviral influenza vaccines.