Separation of Acidic and Basic Proteins by Nanoparticle-Filled Capillary Electrophoresis

• Published in: Analytical chemistry (Washington) Vol. 78; no. 23; pp. 8004 - 8010
• Main Authors: Yu, Cheng-Ju, Su, Chih-Lin, Tseng, Wei-Lung
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 01.12.2006
• Subjects: Acids - chemistry; Alkalies - chemistry; Analytical chemistry; Animals; Biochemistry; Biological samples; Cattle; Chemistry; Chickens; Chromatographic methods and physical methods associated with chromatography; Electrophoresis; Electrophoresis, Capillary - methods; Exact sciences and technology; Gold; Gold - chemistry; Horses; Humans; Hydrogen-Ion Concentration; Nanoparticles; Nanostructures - chemistry; Nanostructures - ultrastructure; Other chromatographic methods; Particle Size; Polymers; Proteins; Proteins - analysis; Proteins - chemistry; Proteins - metabolism; Reactors; Saliva - chemistry; Saliva - metabolism; Scientific apparatus & instruments; Spectrum Analysis; Phosphates; Resolving power; Gold; Capillary electrophoresis; Nanoparticle; Polymer; Coatings; Protein; Blood plasma; Biological compound; Reversed flow; Efficiency; Reproducibility; Electroosmosis; Bromides; Standard deviation
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac061059c

We present the first example of the analysis of acidic and basic proteins by nanoparticle-filled capillary electrophoresis. Compared to the didodecyldimethylammonium bromide (DDAB)-coated capillary, the DDAB-capped gold nanoparticles (AuNPs) as pseudostationary phase were found to form more stable coating on the capillary wall, thus leading to greater separation efficiency and high reproducibility. In addition to their advantages for protein separation, DDAB-capped AuNPs can generate high reversed electroosmotic flow, which is 75% greater than DDAB at pH 3.5. To allow strong interactions with proteins, the AuNPs were modified with poly(ethylene oxide) via noncovalent bonding to form gold nanoparticles/polymer composites (AuNPPs). Using a capillary dynamically coated with DDAB-capped AuNPs and filled with AuNPPs under acidic conditions (10 mM phosphate, pH 3.5), we have demonstrated the separation of acidic and basic proteins with peak efficiencies ranging from 71 000 to 1 007 000 plates/m and relative standard deviations of migration time less than 0.6%. Additionally, the proposed method has been applied to the analyses of biological samples, including saliva, red blood cells, and plasma. With simplicity, high resolving power, and high reproducibility, the proposed method has shown great potential for proteomics applications and clinical diagnosis.