Bioconjugation of 32-macrocyclic polyammonium cations-functionalized gold nanoparticles with BSA

Water-dispersed, spherical, underivatized Au-NPs with particle size less than 5 nm were synthesized from an aqueous solution of 32-macrocyclic polyammonium chloride, [32]ane-(NH2+)8·8Cl- (32-MCPAC) using sodium borohydride (NaBH4) as the reducing agent. The bioconjugation of the synthesized Au-NPs at different pHs (3.6–5.6) with bovine serum albumin (BSA) protein was studied using UV–Vis, fluorescence, and Raman spectroscopy. These studies support that the Au-NPs were incorporated into the protein moiety and bound to it chemically. The binding constants (Kb) and stoichiometries (n) (i.e., the number of Au-NPs bound by the proteins) of BSA protein to the Au-NPs at different pHs were determined by measuring the quenching of the fluorescence intensity of the tryptophan residues of the protein molecules after conjugation. The values for Kb (n) were found to be 1.05 × 1010 M−1 (1.66), 2.09 × 1010 M−1 (2.30), and 1.86 × 1010 M−1 (1.75) at pH 3.60, 4.60, and 5.60 for BSA–Au-NPs conjugations, respectively. The results show that BSA binds to the Au-NPs strongly at pH 4.60, which is equivalent to its isoelectric point (pI 4.6).

32-macrocyclic polyammonium chloride, [32]ane-(NH2+)8·8Cl- (32-MCPAC) stabilized water dispersed Au-NPs conjugate with biomolecule, BSA. BSA strongly binds Au-NPs at the isoelectric point (pI = 4.6).Figure optionsDownload high-quality image (50 K)Download as PowerPoint slide