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Highly Sensitive and Selective Strategy for MicroRNA Detection Based on WS_2 Nanosheet Mediated Fluorescence Quenching and Duplex-Specific Nuclease Signal Amplification

机译:基于WS_2纳米片介导的荧光猝灭和双特异性核酸酶信号放大的高灵敏度和选择性的MicroRNA检测策略。

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摘要

MicroRNAs (miRNAs) play vital roles in physiologic and pathologic processes and are significant biomarkers for disease diagnostics and therapeutics. However, rapid, low-cost, sensitive, and selective detection of miRNAs remains a challenge because of their short length, sequence homology, and low abundance. Herein, we report for the first time that WS_2 nanosheet can exhibit differential affinity toward short oligonucleotide fragment versus ssDNA probe and act as an efficient quencher for adsorbed fluorescent probes. This finding is utilized to develop a new strategy for simple, sensitive, and selective detection of miRNA by combining WS_2 nanosheet based fluorescence quenching with duplex-specific nuclease signal amplification (DSNSA). This assay exhibits highly sensitive and selective with a detection limit of 300 fM and even discriminate single-base difference between the miRNA family members. The result indicates that this simple and cost-effective strategy holds great potential application in biomedical research and clinical diagnostics.
机译:MicroRNA(miRNA)在生理和病理过程中起着至关重要的作用,并且是疾病诊断和治疗的重要生物标记。但是,由于miRNA的长度短,序列同源性和丰度低,因此快速,低成本,灵敏和选择性检测仍然是一个挑战。在本文中,我们首次报道WS_2纳米片相对于ssDNA探针对短寡核苷酸片段表现出不同的亲和力,并充当吸附的荧光探针的有效淬灭剂。通过结合基于WS_2纳米片的荧光淬灭和双链体特异性核酸酶信号放大(DSNSA),该发现可用于开发一种简单,灵敏和选择性检测miRNA的新策略。该检测方法具有高度的灵敏度和选择性,检测限为300 fM,甚至可以区分miRNA家族成员之间的单碱基差异。结果表明,这种简单且具有成本效益的策略在生物医学研究和临床诊断中具有巨大的潜在应用。

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