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PCR-free quantitative detection of genetically modified organism from raw materials – A novel electrochemiluminescence-based bio-barcode method

机译:无PCR的原材料中转基因生物定量检测–一种基于电化学发光的新型生物条形码方法

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摘要

Bio-barcode assay based on oligonucleotide-modified gold nanoparticles (Au-NPs) provides a PCR-free method for quantitative detection of nucleic acid targets. However, the current bio-barcode assay requires lengthy experimental procedures including the preparation and release of barcode DNA probes from the target-nanoparticle complex, and immobilization and hybridization of the probes for quantification. Herein, we report a novel PCR-free electrochemiluminescence (ECL)-based bio-barcode assay for the quantitative detection of genetically modified organism (GMO) from raw materials. It consists of tris-(2’2’-bipyridyl) ruthenium (TBR)-labele barcode DNA, nucleic acid hybridization using Au-NPs and biotin-labeled probes, and selective capture of the hybridization complex by streptavidin-coated paramagnetic beads. The detection of target DNA is realized by direct measurement of ECL emission of TBR. It can quantitatively detect target nucleic acids with high speed and sensitivity. This method can be used to quantitatively detect GMO fragments from real GMO products.
机译:基于寡核苷酸修饰的金纳米颗粒(Au-NPs)的生物条形码分析提供了无PCR的定量检测核酸靶标的方法。然而,当前的生物条形码测定需要冗长的实验程序,包括从靶-纳米颗粒复合物中制备和释放条形码DNA探针,以及固定和杂交探针以进行定量。在这里,我们报告了一种新颖的无PCR的基于化学发光(ECL)的生物条形码检测方法,用于从原材料中定量检测转基因生物(GMO)。它由tris-(2′2′-联吡啶基)钌(TBR)条形码条形码DNA,使用Au-NP和生物素标记的探针进行核酸杂交,以及通过链霉亲和素包被的顺磁珠选择性地捕获杂交复合物。通过直接测量TBR的ECL发射可实现目标DNA的检测。它可以快速,灵敏地定量检测目标核酸。该方法可用于定量检测真实GMO产品中的GMO片段。

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