Label-Free Immunoassay for Sensitive and Rapid Detection of the SARS-CoV-2 Antigen Based on Functionalized Magnetic Nanobeads with Chemiluminescence and Immunoactivity

被引:40
|
作者
Wang, Shanshan [1 ]
Shu, Jiangnan [1 ]
Lyu, Aihua [1 ]
Huang, Xiaoxue [2 ]
Zeng, Weihong [2 ]
Jin, Tengchuan [2 ]
Cui, Hua [1 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Soft Matter Chem, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Lab Struct Immunol, CAS Key Lab Innate Immun & Chron Dis, CAS Ctr Excellence Mol Cell Sci,Div Life Sci & Me, Hefei 230027, Anhui, Peoples R China
关键词
AU-AT-AG; GOLD NANOPARTICLES;
D O I
10.1021/acs.analchem.1c03208
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Direct detection of SARS-CoV-2 in biological specimens is often challenging due to the low abundance of viral components and lack of enough sensitivity. Herein, we developed a new type of chemiluminescent functionalized magnetic nanomaterial for sensitive detection of the SARS-CoV-2 antigen. First, HAuCl4 was reduced by N-(aminobutyl)-N-(ethylisoluminol) (ABEI) in the presence of amino magnetic beads (MB-NH2) to generate ABEI-AuNPs, which were directly assembled on the surface of MB-NH2. Then, Co2+ was modified onto the surface to form MB@ABEI-Au/Co2+ (MAA/Co2+). MAA/Co2+ exhibited good chemiluminescence (CL) and magnetic properties. It was also found that it was easy for the antibody to be connected with MAA/Co2+. Accordingly, MAA/Co2+ was used as a sensing interface to construct a label-free immunoassay for rapid detection of the N protein in SARS-CoV-2. The immunoassay showed a linear range from 0.1 pg/mL to 10 ng/mL and a low detection limit of 69 fg/mL, which was superior to previously reported methods for N protein detection. It also demonstrated good selectivity by virtue of magnetic separation, which effectively removed a sample matrix after immunoreactions. It was successfully applied for the detection of the N protein in spiked human serum and saliva samples. Furthermore, the immunoassay was integrated with an automatic CL analyzer with magnetic separation to detect the N protein in patient serums and rehabilitation patient serums with satisfactory results. Thus, the CL immunoassay without a complicated labeling procedure is sensitive, selective, fast, simple, and cost-effective, which may be used to combat the COVID-19 pandemic. Finally, the CL quenching mechanism of the N protein in the immunoassay was also explored.
引用
收藏
页码:14238 / 14246
页数:9
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