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

机译:通过脱氧核糖核酸级联和视觉信号读出来检测无标记病原体

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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.
机译:已经开发了基于比色核酸的无标记病原体检测技术,并将其用于Zika病毒检测。该测试依赖于病毒RNA的基于核酸序列的扩增(NASBA),然后通过构成可视分裂型脱氧核糖核酸酶(vsDz)探针的级联的脱氧核糖核酸酶对扩增子进行询问。该探针由分裂的磷酸二酯酶脱氧核酶组成,在与特定的扩增子片段结合后形成其催化核心。催化活性复合物识别并裂解抑制的过氧化物酶样脱氧核酶(PDz),从而使其活化。活性PDz催化过氧化氢介导的无色底物氧化成有色产物,从而产生可见信号。病毒RNA(10(6)拷贝/ mL或更高)可在2小时内触发强烈的颜色。该测试可选择性区分Zika和密切相关的登革热和西尼罗河病毒。报道的技术将等温扩增和视觉检测相结合,因此代表了未来发展的一种成本效益高且无需仪器的现场护理核酸分析方法的基础。

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