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Sub-femtomolar detection of DNA and discrimination of mutant strands using microwell-array assisted digital enzyme-linked oligonucleotide assay

机译:使用微孔阵列辅助数字酶联寡核苷酸测定的微孔阵列DNA对DNA和突变链的区分

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Detection methods that do not rely on the amplification of DNA but can reach sensitivity, specificity and throughput of gold standard methods, such as qPCR, have been extensively explored in recent years. Here, we present a hydrophilic-in-hydrophobic (HIH)-microwell array platform that empowers a panel of different amplification-free DNA bioassays: digital enzyme-linked oligonucleotide assay (ELONA), ligation-assisted (LA) digital ELONA and so-called ‘analog’ bioassays. We developed all three bioassays by using magnetic beads for capturing DNA target, followed by hybridization of enzyme-labelled detection probes and sealing of the built complexes into the femtoliter HIH microwells to achieve the fluorescent readout of single DNA molecules. With the optimized digital ELONA bioassay, we successfully detected 97 and 200?nt-long ssDNA molecules down to 68 and 92 aM, respectively, demonstrating extremely high sensitivity of the bioassay and its flexibility towards targets of different lengths. Importantly, we also proved that the same bioassay concept was suited to detect substantially higher concentrations of ssDNA (up to picomolar levels) by quantifying the total fluorescent intensity rather than counting fluorescent events for digital quantification. Finally, we advanced this concept towards LA digital ELONA capable of differentiating wildtype strands from those carrying single-point mutations even when the former were constituting only 1% of the DNA mixture and were present at 2?fM concentration. In conclusion, the developed platform showed remarkably high sensitivity, specificity and versatility for amplification-free detection of DNA and as such can be valuable for numerous applications in medical diagnostics, gene analysis, food safety and environmental monitoring.
机译:近年来,不依赖DNA扩增但能够达到敏感性,特异性和吞吐量,例如QPCR,近年来,检测方法已被广泛探讨QPCR,如QPCR,如QPCR,都已广泛探讨。在这里,我们提出了一种亲水性 - 疏水性(HIH)-MICROWELL阵列平台,其赋予了无扩增DNA生物测定的面板:数字酶联寡核苷酸测定(ELONA),连接辅助(LA)数字ELONA和SO-称为“模拟”生物测定。我们通过使用用于捕获DNA靶标的磁珠开发了所有三种生物测定,然后通过将酶标记的检测探针杂交和内置复合物的密封到Femtoliter HiH微孔中,以实现单个DNA分子的荧光读数。通过优化的数字Elona生物测定,我们分别成功地检测到97和200?NT-LONG SSDNA分子,分别显示为68和92次,展示生物测定的极高敏感性及其朝向不同长度的靶标的灵活性。重要的是,我们还证明了相同的生物测定概念,通过量化总荧光强度而不是计算数字量化的荧光事件来检测相同的生物测定概念。最后,我们向LA Digital Elona推进了这种概念,能够将野生型股线与携带单点突变的人区分开,即使前者仅均为1%的DNA混合物并以2〜Fm浓度存在。总之,发育平台对DNA的免疫检测显着高的灵敏度,特异性和多功能性,因此对于医学诊断,基因分析,食品安全和环境监测的许多应用可能是有价值的。

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