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Label-Free Pathogen Detection by a Deoxyribozyme Cascade with Visual Signal Readout.


ABSTRACT: 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 (106 copies/mL or higher) triggers intense color within 2 hr. 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.

SUBMITTER: Reed AJ 

PROVIDER: S-EPMC6713451 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

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Label-Free Pathogen Detection by a Deoxyribozyme Cascade with Visual Signal Readout.

Reed Adam J AJ   Connelly Ryan P RP   Williams Allison A   Tran Maithi M   Shim Byoung-Shik BS   Choe Hyeryun H   Gerasimova Yulia V YV  

Sensors and actuators. B, Chemical 20181129


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 catal  ...[more]

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