Lin Chi-Chang, Yang Ying-Mei, Chen Yan-Fu, Yang Tzyy-Schiuan, Chang Hsien-Chang
Institute of Biomedical Engineering, National Cheng Kung University, Tainan 701, Taiwan, ROC.
Biosens Bioelectron. 2008 Oct 15;24(2):178-83. doi: 10.1016/j.bios.2008.03.035. Epub 2008 Apr 4.
A unique, sensitive, highly specific, and photobleaching-resistant immunoassay system utilizing gold nanoparticles and surface-enhanced Raman scattering (SERS) is described. This new system, featuring a capability of bifunctional analysis, is manufactured by chemisorption of antibody immunoglobulin G (IgG) on gold nanoparticles (AuNP), followed by coupling the Raman-active reporter molecule, 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) to the surface of IgG-AuNP. The adsorbed DTNB molecules exhibit strong Raman signals via both electromagnetic and chemical enhancement. The narrow spectral widths and high photostability assure the system to be an excellent detection label. This SERS-based immunoassay is applied to the detection of protein A, which is a specific surface antigen of Staphylococcus aureus. A working curve is obtained by plotting the intensity of the SERS signal of symmetric NO(2) stretching of DTNB at 1,333 cm(-1) versus the concentration of the analyte (antigen). A dynamic range of two to three orders of magnitude and a detection limit of 1 pg/mL of protein A are achieved.
本文描述了一种利用金纳米颗粒和表面增强拉曼散射(SERS)的独特、灵敏、高度特异且抗光漂白的免疫分析系统。这种具有双功能分析能力的新系统,是通过将抗体免疫球蛋白G(IgG)化学吸附在金纳米颗粒(AuNP)上,然后将拉曼活性报告分子5,5'-二硫代双(2-硝基苯甲酸)(DTNB)偶联到IgG-AuNP表面而制成的。吸附的DTNB分子通过电磁增强和化学增强展现出强烈的拉曼信号。狭窄的光谱宽度和高光稳定性确保该系统成为出色的检测标记物。这种基于SERS的免疫分析方法应用于金黄色葡萄球菌的特异性表面抗原蛋白A的检测。通过绘制1333 cm⁻¹处DTNB对称NO₂伸缩振动的SERS信号强度与分析物(抗原)浓度的关系曲线,得到了工作曲线。实现了两个到三个数量级的动态范围和1 pg/mL蛋白A的检测限。