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Colorimetric Detection of Nucleic Acids through Triplex-Hybridization Chain Reaction and DNA-Controlled Growth of Platinum Nanoparticles on Graphene Oxide

机译:通过三重杂交链反应和铂纳米粒子对氧化铂纳米颗粒的DNA控制的比色检测

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摘要

The controllable growth of metal nanoparticles on nanomaterials is becoming a useful strategy for developing nanocomposites with designated performance. Here, a DNA-controlled strategy for growth of Pt nanoparticles on graphene oxide (GO-PtNPs) to regulate the nanozyme activity and a triplex-hybridization chain reaction (tHCR) for triggering the assembly of DNA probes to amplify the target-induced nanozyme catalytic signal were designed. The tHCR with one linear and two hairpin probes could be specially triggered by a tHCR trigger to form a long double-stranded DNA structure in the presence of target nucleic acid, which hindered the adsorption of these probes on a GO surface, and thus accelerated the growth of PtNPs. The formed GO-PtNPs showed strong catalytic activity toward the oxidation of 3,3,5,5-tetramethylbenzidine, thereby producing an amplified "turn-on" detection signal. The proposed method showed very high sensitivity with the detection limits down to 14.6 pM for mutant KRAS DNA and 21.7 pM for let-7a microRNA. This method was validated with better analytical performance than a general HCR system and could be effectively used for the identification of single-nucleotide polymorphisms, thus providing a novel approach for simple and sensitive detection of nucleic acids.
机译:金属纳米颗粒对纳米材料的可控生长正在成为开发具有指定性能的纳米复合材料的有用策略。这里,用于将氧化烯氧化物(GO-PTNPS)上的Pt纳米颗粒生长的DNA控制策略,以调节纳米酶活性和三重交杂化链反应(ThCr),用于引发DNA探针的组装以扩增靶诱导的纳佐催化剂信号被设计。具有一个线性和两个发夹探针的ThCr可以通过Thcr触发专门触发,以在靶核酸存在下形成长的双链DNA结构,这阻碍了这些探针在去表面上的吸附,从而加速了PTNP的生长。所形成的GO-PTNPS显示出朝向3,3,5,5-四甲基苯胺的氧化的强催化活性,从而产生扩增的“开启”检测信号。该方法显示出非常高的灵敏度,对突变体KRADNA的检测限额为14.6μm,对于Let-7a microRNA的21.7μmPM。通过更好的分析性能验证该方法,而不是一般的HCR系统,可以有效地用于鉴定单核苷酸多态性,从而提供一种用于核酸的简单敏感性检测的新方法。

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