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A DNAzyme-amplified DNA circuit for highly accurate microRNA detection and intracellular imaging

机译:用于高精度微小RNA检测和细胞内成像的DNAzyme扩增DNA电路

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Biomolecular self-assembly circuits have been well developed for high-performance biosensing and bioengineering applications. Here we designed an isothermal concatenated nucleic acid amplification system which is composed of a lead-in catalyzed hairpin assembly (CHA), intermediate hybridization chain reaction (HCR) and ultimate DNAzyme amplifier units. The analyte initiates the self-assembly of hairpin reactants into dsDNA products in CHA, which generates numerous trigger sequences for activating the subsequent HCR-assembled long tandem DNAzyme nanowires. The as-acquired DNAzyme catalyzed the successive cleavage of its substrates, leading to an amplified fluorescence readout. The sophisticated design of our CHA-HCR-DNAzyme scheme was systematically investigated in vitro and showed dramatically enhanced detection performance. As a general sensing strategy, this CHA-HCR-DNAzyme method enables the amplified analysis of miRNA and its accurate intracellular imaging in living cells, originating from their synergistic signal amplifications. This method shows great potential for analyzing trace amounts of biomarkers in various clinical research studies.
机译:为高性能生物传感和生物工程应用已经开发了生物分子自组装电路。在这里,我们设计了一种等温级联核酸扩增系统,其由铅催化的发夹组合(CHA),中间杂交链反应(HCR)和最终的DNAzyme放大器单元组成。分析物将发夹反应物的自组装成CHA中的DSDNA产物,其产生许多触发序列,用于激活随后的HCR组装的长串联DNAzyme纳米线。 AS获取的DNazyme催化其基材的连续切割,导致扩增的荧光读数。在体外系统地研究了CHA-HCR-DNAzyme方案的复杂设计,并显着提高了检测性能。作为普通传感策略,这种CHA-HCR-DNAzyme方法能够在生物细胞中进行MiRNA的分析及其精确的细胞内成像,源自其协同信号放大。该方法显示出分析各种临床研究研究中痕量生物标志物的巨大潜力。

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