Luo Lin, Liu Zhao, Li Jianjun, Zhu Jian
J Nanosci Nanotechnol. 2014 Jun;14(6):4036-42. doi: 10.1166/jnn.2014.8224.
A novel immunosensor of human immune globulin (IgG) was fabricated based on the fluorescence transfer between luminescent semiconductor quantum dots (QDs) and gold nanoparticles (AuNPs). AuNPs and CdSe/ZnS QDs were respectively labeled with immune reaction pair:IgG and goat anti-human immunoglobulin (GIgG), by optimizing the conditions including pH value and protein amount. In the assembled QD-GIgG-IgG-AuNP fluorescence resonance energy transfer (FRET) immunocomplex system, the presence of AuNP-IgG directly reduced the fluorescence intensity of the GIgG conjugated QDs. As a result, the concentration of AuNP-IgG had a linear relationship with the fluorescence decrease in a range of 0-1.57 microg/mL. Furthermore, the mechanism of the QDs' fluorescence decay has also been discussed and attributed to the light-induced photobleaching. This novel sensing method achieves quantitative detection of trace proteins, suggesting the potential of biomolecule-AuNPs conjugation based analytical methods in further application.
基于发光半导体量子点(QDs)与金纳米颗粒(AuNPs)之间的荧光转移,构建了一种新型的人免疫球蛋白(IgG)免疫传感器。通过优化pH值和蛋白量等条件,分别用免疫反应对IgG和羊抗人免疫球蛋白(GIgG)标记AuNPs和CdSe/ZnS QDs。在组装好的QD-GIgG-IgG-AuNP荧光共振能量转移(FRET)免疫复合物系统中,AuNP-IgG的存在直接降低了与GIgG偶联的QDs的荧光强度。结果,在0-1.57μg/mL范围内,AuNP-IgG的浓度与荧光降低呈线性关系。此外,还讨论了QDs荧光衰减的机制,并将其归因于光致光漂白。这种新型传感方法实现了对痕量蛋白质的定量检测,表明基于生物分子-AuNPs共轭的分析方法在进一步应用中的潜力。