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Phage-mediated counting by the naked eye of miRNA molecules at attomolar concentrations in a Petri dish

机译:皮氏培养皿中attomolar浓度的miRNA分子的噬菌体介导计数

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摘要

The ability to count biomolecules such as cancer-biomarker miRNAs with the naked eye is seemingly impossible in molecular diagnostics. Here, we show an ultrasensitive naked-eye-counting strategy for quantifying miRNAs by employing T7 phage—a bacteria-specific virus nanoparticle—as a surrogate. The phage is genetically engineered to become fluorescent and capable of binding a miRNA-capturing gold nanoparticle (GNP) in a one-to-one manner. Target miRNAs crosslink the resultant phage–GNP couple and miRNA-capturing magnetic microparticles, forming a sandwich complex containing equimolar phage and miRNA. The phage is then released from the complex and developed into one macroscopic fluorescent plaque in a Petri dish by plating it in a host bacterial medium. Counting the plaques by the naked eye enables the quantification of miRNAs with detection limits of ~3 and ~5 aM for single-target and two-target miRNAs, respectively. This approach offers ultrasensitive and convenient quantification of disease biomarkers by the naked eye.
机译:在分子诊断中,用肉眼计数生物分子(例如癌症生物标志物miRNA)的能力似乎是不可能的。在这里,我们展示了一种超敏感的肉眼计数策略,可通过采用T7噬菌体(一种细菌特异性病毒纳米颗粒)作为替代物来量化miRNA。噬菌体经过基因改造后可以发出荧光,并能够以一对一的方式结合捕获miRNA的金纳米颗粒(GNP)。目标miRNA交联所得的噬菌体-GNP对和捕获miRNA的磁性微粒,形成包含等摩尔噬菌体和miRNA的三明治复合物。然后将噬菌体从复合物中释放出来,并通过将其铺在宿主细菌培养基中而在陪替氏培养皿中显影成一个宏观的荧光噬菌斑。用肉眼计数噬菌斑能够定量检测单靶和双靶miRNA的检测限分别为〜3和〜5 aM的miRNA。这种方法可以通过肉眼对疾病生物标志物进行超灵敏且方便的定量。

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