Yue Shuzhen, Song Xinyue, Song Weiling, Bi Sai
College of Chemistry and Chemical Engineering , Qingdao University , Qingdao 266071 , P. R. China . Email:
Shandong Province Key Laboratory of Detection Technology for Tumor Makers , College of Chemistry and Chemical Engineering , Linyi University , Linyi 276000 , P. R. China.
Chem Sci. 2018 Dec 4;10(6):1651-1658. doi: 10.1039/c8sc04756a. eCollection 2019 Feb 14.
DNA has become a promising material to construct high-order structures and molecular devices owing to its sequence programmability. Herein, a DNA machine based on branched catalytic hairpin assembly (bCHA) is introduced for dynamic self-assembly of DNA dendrimers. For this system, a Y-shaped hairpin trimer tethered with three kinds of hairpins (H1, H2 and H3) is constructed. The introduction of an initiator (I) triggers a cascade of CHA reactions among hairpin trimers, leading to the formation of DNA dendrimers. Through labeling fluorophore/quencher pairs in the hairpin trimers, this catalytic DNA machine is applied as a versatile amplification platform to analyze nucleic acids using microRNA-155 (miR-155) as a model analyte. Benefiting from the "diffusion effect", the proposed bCHA achieves a greatly improved sensitivity in comparison with traditional CHA. This catalytic amplifier exhibits high sensitivity toward miR-155 detection with a dynamic range from 2.5 nM to 500 nM and demonstrates excellent selectivity to distinguish the single-base mismatched sequence from the perfectly complementary one, which is further applied to detect low-abundance miR-155 spiked in complex matrices with minimal interference. This method is further applied for imaging of miR-155 in different live cells. The bCHA reaction can be specifically triggered by intracellular miR-155, achieving monitoring of the dynamic miRNA expression and distribution. Overall, our proposed enzyme-free dynamic DNA self-assembly strategy provides a versatile approach for the development of DNA nanotechnology in biosensing and bioimaging, and monitoring the cellular miRNA-related biological events.
由于其序列可编程性,DNA已成为构建高阶结构和分子器件的一种有前景的材料。在此,介绍一种基于分支催化发夹组装(bCHA)的DNA机器,用于DNA树枝状大分子的动态自组装。对于该系统,构建了一种连接有三种发夹(H1、H2和H3)的Y形发夹三聚体。引入引发剂(I)会触发发夹三聚体之间的一系列CHA反应,导致DNA树枝状大分子的形成。通过在发夹三聚体中标记荧光团/猝灭剂对,这种催化DNA机器被用作通用的扩增平台,以微小RNA-155(miR-155)作为模型分析物来分析核酸。受益于“扩散效应”,与传统CHA相比,所提出的bCHA实现了灵敏度的大幅提高。这种催化放大器对miR-155检测具有高灵敏度,动态范围为2.5 nM至500 nM,并表现出优异的选择性,能够区分单碱基错配序列和完全互补序列,进一步应用于检测复杂基质中掺入的低丰度miR-155,干扰最小。该方法进一步应用于不同活细胞中miR-155的成像。bCHA反应可由细胞内的miR-155特异性触发,实现对动态miRNA表达和分布的监测。总体而言,我们提出的无酶动态DNA自组装策略为DNA纳米技术在生物传感和生物成像中的发展以及监测细胞miRNA相关生物事件提供了一种通用方法。