Aptamer-Linked Photonic Crystal Assay for High-Throughput Screening of HIV and SARS-CoV-2

被引:7
作者
Rizvi, Aysha Sarfraz [1 ]
Murtaza, Ghulam [1 ]
Xu, Xu [1 ]
Gao, Peifeng [1 ]
Qiu, Lili [1 ]
Meng, Zihui [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
RECEPTOR-BINDING DOMAIN; INFLUENZA-VIRUS; APTASENSOR; COVID-19; CAPTURE;
D O I
10.1021/acs.analchem.2c03467
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We present a microplate assay for the detection of HIV and SARS-CoV-2 which involves the preadsorption of carboxy-modified polystyrene microspheres to the microplate wells and their self-assembly leading to the formation of a photonic crystal colloidal array (PCCA). PCCA is then cross linked with amino-modified aptamers selected for viral cell surface glycoproteins, i.e., S1-protein of SARS-CoV-2 and gp120 of the human immunodeficiency virus (HIV), to develop an aptamerlinked photonic crystal assay (ALPA). ALPA is then utilized as a proof-of-concept method for the detection of S1-protein, gp120, and two whole viruses, i.e., SARS-CoV-2 and HIV, as well. The aptamers are stable at room temperature and can bind with the viruses' proteins via hydrogen bonding. This binding leads to color generation from PCCA, and the signal can easily be measured and quantified by a UV/vis spectrometer. The assay carries the advantage of a two-step detection process by the addition of the virus sample directly to a 96-well microplate and incubation of 5 min followed by convenient detection through a UV/vis-spectrometer. The assay does not require any additional reagents and can be customized for similar viruses utilizing specific aptamers targeting their cell surface receptors.
引用
收藏
页码:917 / 923
页数:7
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