Colorimetric detection of influenza A virus using antibody-functionalized gold nanoparticles

被引:105
作者
Liu, Yuanjian [1 ]
Zhang, Linqun [1 ]
Wei, Wei [1 ]
Zhao, Hongyu [2 ]
Zhou, Zhenxian [2 ]
Zhang, Yuanjian [1 ]
Liu, Songqin [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Jiangsu Prov Hi Tech Key Lab Biomed Res, Nanjing 211189, Jiangsu, Peoples R China
[2] Southeast Univ, Affiliated Hosp 2, Cent Lab, Nanjing 210003, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
RECEPTOR-BINDING; MEMBRANE-FUSION; GLYCONANOPARTICLES; POLYNUCLEOTIDES; RECOGNITION; BIOSENSORS; STRATEGY; ASSAY;
D O I
10.1039/c5an00407a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Early and accurate diagnosis is considered the key issue to prevent the further spread of viruses and facilitate influenza therapy. Herein, we report a colorimetric immunosensor for influenza A virus (IAV) based on gold nanoparticles (AuNPs) modified with monoclonal anti-hemagglutinin antibody (mAb). The immunosensor allows for a fast, simple, and selective detection of IAV. In this assay, influenza-specific antibodies are conjugated to AuNPs to create mAb-AuNP probes. Since IAV has multiple recognition sites for probes on the surface, the mAb-AuNP probes can be specifically arranged on the virus surface due to their very specific antigen recognition. In this case, this aggregation of the mAb-AuNP probes produces a red shift in the absorption spectrum due to plasmon coupling between adjacent AuNPs, and it can be detected with the naked eye as a color change from red to purple and quantified with the absorption spectral measurements. The aggregate formation is also confirmed with transmission electron microscopy (TEM) imaging and dynamic light scattering (DLS). Under the optimal conditions, the present immunoassay can sensitively measure H3N2 IAV (A/Brisbane/10/2007) with a detection limit of 7.8 hemagglutination units (HAU). This proposed immunosensor revealed high specificity, accuracy, and good stability. Notably, it is a single-step detection using AuNP probes and UV-vis spectrophotometer for readout, and no additional amplification, e.g., enzymatic, is needed to read the result. This assay depends on an ordered AuNP structure covering the virus surface and can be applied to any virus pathogen by incorporating the appropriate pathogen-specific antibody.
引用
收藏
页码:3989 / 3995
页数:7
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