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Ultrasensitive colorimetric detection of circulating tumor DNA using hybridization chain reaction and the pivot of triplex DNA

机译:使用杂交链反应的循环肿瘤DNA和三醇DNA枢转的超敏感比色检测

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摘要

This work presents an amplified colorimetric biosensor for circulating tumor DNA (ctDNA), which associates the hybridization chain reaction (HCR) amplification with G-Quadruplex DNAzymes activity through triplex DNA formation. In the presence of ctDNA, HCR occurs. The resulting HCR products are specially recognized by one sequence to include one GGG repeat and the other containing three GGG repeats, through the synergetic effect of triplex DNA and asymmetrically split G-Quadruplex forming. Such design takes advantage of the amplification property of HCR and the high peroxidase-like catalytic activity of asymmetrically split G-Quadruplex DNAzymes by means of triplex DNA formation, which produces color signals in the presence of ctDNA. Nevertheless, in the absence of ctDNA, no HCR happens. Thus, no triplex DNA and G-Quadruplex structure is formed, producing a negligible background. The colorimetric sensing platform is successfully applied in complex biological environments such as human blood plasma for ctDNA detection, with a detection limit corresponding to 0.1 pM. This study unambiguously uses triplex DNA forming as the pivot to integrate nucleic acid amplification and DNAzymes for producing a highly sensitive signal with low background.
机译:该工作介绍了用于循环肿瘤DNA(CTDNA)的放大的比色生物传感器,其通过Tiplex DNA形成将杂交链反应(HCR)扩增与G-Quadreplex DNazymes活性相关。在CTDNA存在下,发生HCR。通过三重DNA的协同效果和不对称分裂G-四重复形成,由一种序列特殊地识别得到的HCR产物以包括一个GGG重复,另一个含有三个GGG重复。这种设计利用了HCR的扩增性能和通过三重DNA形成的不对称分离G-Quadflex DNazymes的高过氧化物酶样催化活性,其在CTDNA存在下产生颜色信号。然而,在没有CTDNA的情况下,没有发生任何HCR。因此,没有形成三链DNA和G - 四边形结构,从而产生可忽略的背景。比色感测平台成功地应用于复杂的生物环境,例如用于CTDNA检测的人血浆,检测极限对应于0.1μm。该研究明确地使用Triplex DNA作为枢轴形成,以整合核酸扩增和DNAzymes以产生具有低背景的高敏感信号。

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