Ling Jian, Li Yuan Fang, Huang Cheng Zhi
College of Chemistry and Chemical Engineering, Education Ministry Key Laboratory on Luminescence and Real-Time Analysis, Southwest University, Chongqing 400715, People's Republic of China.
Anal Chem. 2009 Feb 15;81(4):1707-14. doi: 10.1021/ac802152b.
In this contribution, we established a sandwich immunoassay system with a common spectrofluorometer to collect the plasmon resonance scattering (PRS) signals from silver nanoparticles (AgNPs) immunotargeted on glass slides. By taking the immunoreactions of goat antihuman IgG (Fc fragment specific) antibody (GAH-IgG), human immunoglobulin (H-IgG), and rabbit antihuman IgG (Fab fragment specific) antibody (RAH-IgG) as an example, we found that if a primary antibody (GAH-IgG) was first immobilized on the surface of glass slides and applied to capture target antigen (H-IgG), AgNPs-labeled secondary antibody (RAH-IgG) could be employed to detect the target antigen (H-IgG) by forming a sandwich immune complex on the surface of the glass slide. It was found that the PRS signals resulting from the AgNPs immunotargeted on the glass slides could be applied to the quantitative detection of H-IgG target antigen in the range of 10-1000 ng/mL with the limit of determination of 1.46 ng/mL (3sigma) under optimal conditions, which is sensitive and comparable with reported chemiluminescence immunoassays. With a dark-field microscope coupled with a spectral system, we measured the PRS features of single AgNPs immunotargeted on the glass slides, showing that the PRS of single nanoparticles might have potential applications in analytical chemistry. Further findings showed that the strong PRS signals from the AgNPs immunotargeted on the glass slides can be clearly seen and distinguished by naked eyes under the excitation of a common white light-emitting diode (LED) torch. Therefore, a visual PRS immunoassay system can be established easily with common glass slides and an LED torch.
在本论文中,我们建立了一种夹心免疫分析系统,使用普通的荧光分光光度计收集来自玻片上免疫靶向的银纳米颗粒(AgNPs)的等离子体共振散射(PRS)信号。以山羊抗人IgG(Fc片段特异性)抗体(GAH-IgG)、人免疫球蛋白(H-IgG)和兔抗人IgG(Fab片段特异性)抗体(RAH-IgG)的免疫反应为例,我们发现,如果将一抗(GAH-IgG)首先固定在玻片表面以捕获靶抗原(H-IgG),则可以使用AgNPs标记的二抗(RAH-IgG)通过在玻片表面形成夹心免疫复合物来检测靶抗原(H-IgG)。结果发现,玻片上免疫靶向的AgNPs产生的PRS信号可用于在最佳条件下对10 - 1000 ng/mL范围内的H-IgG靶抗原进行定量检测,其测定限为1.46 ng/mL(3σ),该方法灵敏且与已报道的化学发光免疫分析相当。通过结合光谱系统的暗场显微镜,我们测量了玻片上免疫靶向的单个AgNPs的PRS特征,表明单个纳米颗粒的PRS在分析化学中可能具有潜在应用。进一步的研究结果表明,在普通白色发光二极管(LED)手电筒的激发下,肉眼可以清晰地看到并区分玻片上免疫靶向的AgNPs发出的强PRS信号。因此,使用普通玻片和LED手电筒可以轻松建立可视化PRS免疫分析系统。