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Enzyme-free and label-free miRNA detection based on target-triggered catalytic hairpin assembly and fluorescence enhancement of DNA-silver nanoclusters

机译:基于目标触发的催化发夹装配和DNA-银纳米簇的荧光增强,实现无酶和无标记的miRNA检测

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摘要

We herein describe a simple, enzyme-free, and label-free strategy for the detection of miRNA based on target-triggered catalytic hairpin assembly (CHA) and fluorescence enhancement of DNA-silver nanoclusters (DNA-AgNCs). This strategy employs two hairpin probes that are rationally designed to contain AgNCs and guanine (G)-rich DNA sequence, respectively. In principle, the two hairpin probes, which exist independently, form a hybridized complex in the presence of target miRNA through CHA reaction, thereby inducing strong fluorescence signal of AgNCs by the presence of G-rich sequence placed in close proximity. Importantly, target miRNA is released after the first CHA reaction, which promotes another CHA reaction, consequently leading to the significantly enhanced fluorescence signal of AgNCs. Based on this one-step, homogeneous, and isothermal amplification method, we successfully detected the target miRNA with high selectivity and sensitivity. In addition, the practical applicability of this strategy was also demonstrated by analyzing the target miRNA in human serum.
机译:我们在此描述了一种基于目标触发的催化发夹装配(CHA)和DNA银纳米簇(DNA-AgNCs)荧光增强的miRNA检测的简单,无酶和无标签的策略。此策略采用了两个发夹式探针,这些探针经过合理设计,分别包含AgNC和富含鸟嘌呤(G)的DNA序列。原则上,两个独立存在的发夹探针在目标miRNA存在下通过CHA反应形成杂交复合物,从而通过紧密相邻的富G序列的存在诱导AgNC的强荧光信号。重要的是,靶标miRNA在第一个CHA反应后释放,从而促进了另一个CHA反应,因此导致AgNCs的荧光信号明显增强。基于这一一步,均质且等温扩增的方法,我们成功地以高选择性和高灵敏度检测了目标miRNA。此外,通过分析人血清中的靶标miRNA也证明了该策略的实际适用性。

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