A colorimetric method for determination of the prostate specific antigen based on enzyme-free cascaded signal amplification via  peptide-copper(II) nanoparticles

Biotinylated peptide-Cu 2+ nanoparticles (Cu-P NPs) were synthesized via “one-pot” self-assembly. The peptide P conststs of a hydrophobic dipeptide (FF), a tripeptide (KGH), and a biotin moiety attached to the terminal amino group of the Lys residue. The Cu-P NPs contain abundant catalytically active Cu 2+ ions which are liberated by acid-induced dissolution. The released Cu 2+ ions catalyze the oxidization of 3,3′,5,5′-tetramethylbenzidine (TMB) by H 2 O 2 because of their intrinsic peroxidase activity, and this results in the formation of a blue-green coloration. Based on the streptavidin–biotin interaction, the Cu-P NPs were employed to establish an enzyme-free colorimetric method for determination of prostate-specific antigen (PSA) as a model biomarker. Under optimal conditions, the linear response range is 0.001–1 ng mL −1 , with a limit of detection as low as 1 pg mL −1 . Schematic illustration of a colorimetric immunoassay for the prostate specific antigen (PSA) with biotinylated peptide-Cu 2+ nanoparticle (Cu-P NP) as the signal label based on the streptavidin (SA)–biotin interaction. The signal was produced by Cu 2+ -catalyzed oxidization of 3,3′,5,5′-tetramethylbenzidine (TMB). P: KGHFF