Wang Yanyan, Liu Bin
Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, Singapore.
Biosens Bioelectron. 2009 Jul 15;24(11):3293-8. doi: 10.1016/j.bios.2009.04.020. Epub 2009 Apr 22.
Immunoassays are conventional methods for protein detection, which rely on specific antibody-antigen recognition. Very few strategies have been developed for signal amplification of immunoassays. In this work, we report a conjugated polymer amplified silica nanoparticle (NP)-based immunoassay for IgG detection. After immobilization of the prime antibody on the NP surface, the NPs are used to capture antigen and Cy3 labeled secondary antibody in a sandwich assay format. The presence of target antigen in solution brings the fluorescent Cy3 molecules to the NP surface. Addition of a cationic conjugated polymer further amplifies the fluorescence signal of the dye, which improves the assay sensitivity and selectivity. Within the tested concentration range, a linear response for IgG detection is observed from 0 to 1 microg/mL with a detection limit of approximately 1.1 ng/mL. Due to the pink color of Cy3 molecules, the assay also allows naked eye detection of IgG with a detection limit of 50 ng/mL. The polymer amplified NP assay represents a simple strategy for antigen detection with high sensitivity and selectivity.
免疫测定是蛋白质检测的传统方法,它依赖于特异性抗体 - 抗原识别。针对免疫测定的信号放大,人们开发的策略非常少。在这项工作中,我们报道了一种基于共轭聚合物放大二氧化硅纳米颗粒(NP)的免疫测定法用于检测IgG。将一抗固定在NP表面后,NP用于以夹心测定形式捕获抗原和Cy3标记的二抗。溶液中目标抗原的存在会使荧光Cy3分子聚集到NP表面。添加阳离子共轭聚合物可进一步放大染料的荧光信号,从而提高测定的灵敏度和选择性。在测试的浓度范围内,观察到IgG检测的线性响应范围为0至1微克/毫升,检测限约为1.1纳克/毫升。由于Cy3分子呈粉红色,该测定法还允许肉眼检测IgG,检测限为50纳克/毫升。聚合物放大的NP测定法是一种用于抗原检测的简单策略,具有高灵敏度和选择性。