环介导等温扩增
化学
转导(生物物理学)
DNA
荧光
核酸内切酶
滚动圆复制
计算生物学
检出限
核酸
小RNA
分子生物学
多重位移放大
聚合酶
信号(编程语言)
重组酶聚合酶扩增
级联
生物物理学
聚合酶链反应
细胞生物学
凝聚体
纳米技术
核酸热力学
杂交探针
寡核苷酸
核糖核酸
DNA聚合酶
信号转导
作者
Jintao Chen,Jintao Chen,Yuhui Shang,Yang Yu,Yali Liu,Jinyang Chen,Jinyang Chen
标识
DOI:10.1021/acs.analchem.5c03949
摘要
In this work, we developed an ultrasensitive method for microRNA (miRNA) sensing based on palindrome-mediated isothermal cascade nicking/polymerization for DNA amplification and fluorescent copper nanoparticle (CuNP) generation for signal transduction. With rational palindrome design, only two DNA hairpins and a pair of enzymes were needed to realize one-pot and two-step miRNA detection. In the first step, the target miRNA unfolded the nicking site-containing RNA Probe that subsequently hybridized with the palindromic sequence-engineered hairpin and initiated multiple isothermal cycles driven by polymerase and endonuclease to complete target recognition and signal amplification. Then, the abundant DNA templates accumulated in the previous step facilely and rapidly guided the in situ generation of fluorescent CuNPs for signal transduction. The efficient isothermal amplification and effortless signal transduction jointly achieved ultrasensitive miRNA-21 sensing with a low detection limit (9.7 fM) in a simple and convenient manner. In addition, thanks to its high selectivity and anti-interference ability, the method was able to unambiguously distinguish cancer cells from normal cells based on the test results of cellular miRNA-21. Moreover, this method also enables the detection of different miRNAs simply by modifying the probe sequence, which demonstrates high sensing versatility and application potential in advanced molecular diagnostics.
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