Gold Nanoparticle Sensor for Homocysteine Thiolactone-Induced Protein Modification

• Published in: Langmuir Vol. 24; no. 8; pp. 4107 - 4113
• Main Authors: Gates, Arther T, Fakayode, Sayo O, Lowry, Mark, Ganea, Gabriela M, Murugeshu, Abitha, Robinson, James W, Strongin, Robert M, Warner, Isiah M
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 15-04-2008
• Subjects: Chemistry; Colloidal state and disperse state; Exact sciences and technology; General and physical chemistry; Gold - chemistry; Homocysteine - analogs & derivatives; Homocysteine - chemistry; Humans; Metal Nanoparticles - chemistry; Metal Nanoparticles - ultrastructure; Microscopy, Electron, Transmission; Physical and chemical studies. Granulometry. Electrokinetic phenomena; Serum Albumin - chemistry; Serum Albumin - ultrastructure; Spectrophotometry; Surface physical chemistry; Temperature; Human; Chemisorption; Modification; Gold; Nanoparticle; Citrate; Transition metal; Serum albumin; Calibration; Mechanism; Protein; Thermal stability; Transmission electron microscopy; Lysine; Residue; Models; Acylation
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la7033142

Homocysteine thiolactone-induced protein modification (HTPM) is a unique post-translational protein modification that is recognized as an emergent biomarker for cardiovascular disease. HTPM involves the site-specific acylation of proteins at lysine residues by homocysteine thiolactone (HTL) to produce protein homocystamide, which has been found at elevated levels in patients with coronary heart disease. Herein, we report the development of a novel gold nanoparticle (GNP) biochemical sensor for detection of protein homocystamide in an in vitro serum protein-based model system. Human serum albumin (HSA) and human sera were subjected to HTPM in vitro to produce HSA−homocystamide or serum protein homocystamide, respectively, which was subsequently treated with citrate-capped GNPs. This GNP sensor typically provided instantaneous visual confirmation of HTPM in the protein model systems. Transmission electron microscopy images of the GNPs in the presence of HSA−homocystamide suggest that modification-directed nanoparticle assembly is the mechanism by which the biochemical sensor produces a colorimetric signal. The resultant nanoparticle−protein assembly exhibited excellent thermal and dilutional stability, which is expected for a system stabilized by chemisorption and intermolecular disulfide bonding. The sensor typically provided a linear response for modified human sera concentrations greater than ∼5 mg/mL. The calculated limit of detection and calibration sensitivity for the method in human sera were 5.2 mg/mL and 13.6 AU · (μg/mL)-1, respectively.