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Immunoassay using surface-enhanced Raman scattering based on aggregation of reporter-labeled immunogold nanoparticles

机译:基于报告标记的免疫金纳米粒子聚集的表面增强拉曼散射免疫分析

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摘要

A one-step homogenous sensitive immunoassay using surface-enhanced Raman scattering (SERS) has been developed. This strategy is based on the aggregation of Raman reporter-labeled immunogold nanoparticles induced by the immunoreaction with corresponding antigens. The aggregation of gold nanoparticles results in a SERS signal increase of the Raman reporter. Therefore, human IgG could be directly determined by measuring the Raman signal of the reporter. The process of aggregation was investigated by transmission electron microscopy (TEM) and UV-Vis absorption spectroscopy. The effects of the temperature, time, and size of gold nanoparticles on the sensitivity of the assay were examined. Using human IgG as a model protein, a wide linear dynamic range (0.1-15 mu g mL(-1)) was reached with low detection limit (0.1 mu g mL(-1)) under optimized assay conditions. The successful test suggests that the application of the proposed method holds promising potential for simple, fast detection of proteins in the fields of molecular biology and clinical diagnostics.
机译:已开发出一种使用表面增强拉曼散射(SERS)进行的一步均质敏感免疫测定。该策略基于与相应抗原的免疫反应诱导的拉曼报告分子标记的免疫金纳米颗粒的聚集。金纳米颗粒的聚集导致拉曼报道分子的SERS信号增加。因此,可以通过测量报告基因的拉曼信号直接测定人IgG。通过透射电子显微镜(TEM)和紫外-可见吸收光谱研究了聚集的过程。检查了金纳米颗粒的温度,时间和大小对测定灵敏度的影响。使用人IgG作为模型蛋白,在优化的测定条件下,可以达到较宽的线性动态范围(0.1-15μg mL(-1)),而检测限较低(0.1μg mL(-1))。成功的测试表明,所提出的方法的应用在分子生物学和临床诊断领域中具有简单,快速检测蛋白质的潜力。

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