Label-free pathogen detection by a deoxyribozyme cascade with visual signal readout

被引:12
|
作者
Reed, Adam J. [1 ]
Connelly, Ryan P. [1 ]
Williams, Allison [1 ]
Tran, Maithi [1 ]
Shim, Byoung-Shik [2 ]
Choe, Hyeryun [2 ]
Gerasimova, Yulia, V [1 ]
机构
[1] Univ Cent Florida, Chem Dept, Orlando, FL 32816 USA
[2] Scripps Res Inst, Dept Immunol & Microbiol, Jupiter, FL 33458 USA
基金
美国国家卫生研究院;
关键词
Pathogen detection; Isothermal amplification; Deoxyribozyme cascade; G-quadruplex peroxidase; Colorimetric test; NASBA; SEQUENCE-BASED AMPLIFICATION; NUCLEIC-ACID DETECTION; HEPATITIS-A VIRUS; 16S RIBOSOMAL-RNA; ZIKA VIRUS; BINARY DEOXYRIBOZYME; MOLECULAR-DETECTION; BASIC KIT; DNA; NASBA;
D O I
10.1016/j.snb.2018.11.147
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A colorimetric nucleic acid based test for label-free pathogen detection has been developed and used for the detection of the Zika virus. The test relies on nucleic acid sequence-based amplification (NASBA) of a viral RNA followed by interrogation of the amplicon by a cascade of deoxyribozymes constituting a visual split deoxyribozyme (vsDz) probe. The probe consists of a split phosphodiesterase deoxyribozyme, which forms its catalytic core upon binding to a specific amplicon fragment. The catalytically active complex recognizes and cleaves an inhibited peroxidase-like deoxyribozyme (PDz), thereby activating it. Active PDz catalyzes hydrogen peroxide-mediated oxidation of a colorless substrate into a colored product, thereby generating a visible signal. Viral RNA (10(6) copies/mL or higher) triggers intense color within 2 h. The test selectively differentiates between Zika and closely related dengue and West Nile viruses. The reported technology combines isothermal amplification and visual detection and therefore represents a basis for the future development of a cost-efficient and instrument-free method for point-of-care nucleic acid analysis.
引用
收藏
页码:945 / 951
页数:7
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