Single-Molecule-Based Detection of Conserved Influenza A Virus RNA Promoter Using a Protein Nanopore

被引:20
|
作者
Oh, Sohee [1 ,2 ]
Lee, Mi-Kyung [1 ]
Chi, Seung-Wook [1 ,2 ]
机构
[1] Korea Res Inst Biosci & Biotechnol KRIBB, Div Biomed Res, Dis Target Struct Res Ctr, Daejeon 34141, South Korea
[2] Univ Sci & Technol, KRIBB Sch Biosicence, Dept Proteome Struct Biol, Daejeon 34113, South Korea
基金
新加坡国家研究基金会;
关键词
biological nanopore; alpha-hemolysin; Influenza A virus; RNA promoter; DNA probe; ACCURACY; TESTS; DNA;
D O I
10.1021/acssensors.9b01558
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Influenza A viruses (IAVs) cause annual epidemic and severe pandemic outbreaks worldwide and result in high mortality. Despite the importance of surveillance for preventing IAV infection, the existing techniques are inefficient for ultrasensitive diagnosis in real time. In this study, we performed protein nanopore-based measurements to detect the highly conserved IAV RNA promoter at the single-molecule level. The binding of specific DNA probes to the IAV RNA promoter generated two types of characteristic nanopore signatures with single or double spikes of current blockade and substantially increased dwell times, which facilitated the discrimination of the IAV promoter from nonspecific macromolecules. Our DNA probe-mediated nanopore sensor will serve as an ultrasensitive, real-time, point-of-care diagnostic tool for highly pathogenic IAVs.
引用
收藏
页码:2849 / 2853
页数:9
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