NML, Institute of Mechanics, Chinese Academy of Sciences, 100190 Beijing, China.
Langmuir. 2012 Dec 21;28(51):17718-25. doi: 10.1021/la303032f. Epub 2012 Dec 12.
Carbon disulfide (CS(2)) can spontaneously react with amine groups to form dithiocarbamates on gold surface, providing the possibility to immobilize some compounds with primary or secondary amine groups in one step. Using this principle, an immunosensor interface prepared for immunoglobulin G (IgG) sensing surface toward anti-IgG has been fabricated for the first time by simply immersing gold slides into a mixed aqueous solution of CS(2) and protein A, followed by incubation in immunoglobulin G solution. The reaction between CS(2) and protein A has been followed by UV-vis spectroscopy, whereas cyclic voltammetry has been employed in the characterization of the modified gold surface with CS(2) and protein A, both methods indicating that protein A immobilization is implemented by CS(2). Conventional ellipsometry, atomic force microscopy (AFM), as well as surface plasmon resonance (SPR) have been used to evaluate the specific binding of protein A with IgG and IgG with anti-IgG, revealing that IgG is specifically captured to form the biosensing interface, maintaining its bioactivity. Compared to direct adsorption of IgG on the gold surface, the IgG sensing surface constructed of CS(2) and protein A is far more sensitive to capture anti-IgG as its target molecule. In addition, the modified surface is proven to have good capability to inhibit nonspecific adsorption, as supported by control experiments using lysozyme and BSA. To conclude, antibody immobilization using this one-step method has potential as a simple and convenient surface modification approach for immunosensor development.
二硫化碳(CS(2))可以自发地与胺基反应,在金表面形成二硫代氨基甲酸盐,为一步固定具有伯胺或仲胺基的某些化合物提供了可能性。基于这一原理,我们首次通过简单地将金片浸入 CS(2)和蛋白 A 的混合水溶液中,然后在免疫球蛋白 G 溶液中孵育,制备了用于免疫球蛋白 G 传感表面的免疫传感器界面。CS(2)和蛋白 A 之间的反应通过紫外可见光谱进行了跟踪,而循环伏安法则用于 CS(2)和蛋白 A 修饰金表面的表征,这两种方法都表明蛋白 A 的固定是通过 CS(2)实现的。传统的椭圆测量法、原子力显微镜(AFM)以及表面等离子体共振(SPR)被用于评估蛋白 A 与 IgG 以及 IgG 与抗 IgG 的特异性结合,结果表明 IgG 特异性地被捕获以形成生物传感界面,保持其生物活性。与 IgG 直接吸附在金表面相比,CS(2)和蛋白 A 构建的 IgG 传感表面对作为其靶分子的抗 IgG 的捕获更为敏感。此外,通过使用溶菌酶和 BSA 进行的对照实验,证明了修饰后的表面具有良好的抑制非特异性吸附的能力。总之,使用这种一步法进行抗体固定具有作为简单方便的免疫传感器开发表面修饰方法的潜力。