Palindrome-Mediated Isothermal Cascade DNA Amplification and Effortless Nanosignal Transduction for One-Pot and Ultrasensitive miRNA Sensing

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Jintao Chen, , , Yuhui Shang, , , Yu Yang, , , Yali Liu, , and , Jinyang Chen*, 
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Abstract

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.

Abstract Image

Abstract Image

回文介导的等温级联DNA扩增和毫不费力的纳米信号转导,用于单锅和超灵敏的miRNA传感
在这项工作中,我们开发了一种基于回文介导的等温级联刻蚀/聚合的microRNA (miRNA)超灵敏传感方法,用于DNA扩增和荧光铜纳米颗粒(CuNP)的产生,用于信号转导。通过合理的回文设计,只需要两个DNA发夹和一对酶就可以实现一锅两步的miRNA检测。在第一步中,目标miRNA展开含有缺口位点的RNA探针,随后与回文序列工程发夹杂交,并在聚合酶和核酸内切酶的驱动下启动多个等温循环,完成目标识别和信号扩增。然后,在前一步中积累的丰富的DNA模板方便、快速地指导了荧光CuNPs的原位生成,用于信号转导。高效的等温扩增和轻松的信号转导共同实现了低检出限(9.7 fM)的超灵敏miRNA-21传感,且简单方便。此外,由于其高选择性和抗干扰能力,该方法可以根据细胞miRNA-21的检测结果明确区分癌细胞和正常细胞。此外,该方法还可以通过修改探针序列来检测不同的mirna,这在高级分子诊断中具有很高的传感通用性和应用潜力。
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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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