Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, China.
Department of Chemistry, New York University, New York, NY, 10003, USA.
Small. 2020 Nov;16(47):e2004518. doi: 10.1002/smll.202004518. Epub 2020 Nov 3.
miRNAs, a class of endogenous noncoding RNAs, are involved in many crucial biological processes, which have emerged as a new set of biomarkers for disease theranostics. Exploring efficient signal amplification strategy is highly desired to pursue a highly sensitive miRNA biosensing platform. DNA nanotechnology shows great promise in the fabrication of amplified miRNA biosensors. In this work, a novel DNA walking and rolling nanomachine is developed for highly sensitive and selective detection of miRNA. Particularly, this approach programs two forms of dynamic DNA nanomachines powered by corresponding enzymes, which are well integrated. It is able to achieve a limit of detection as low as 39 × 10 m, along with excellent anti-interfering performance and clinical applications. In addition, by designing pH-controlled detachable intermolecular DNA triplex, the main sensing elements can be conveniently reset, which fulfills the requirements of point-of-care profiling of miRNA. The high consistency between the proposed approach and quantitative real-time polymerase chain reaction validates the robustness and reliability. Therefore, it is anticipated that the DNA walking and rolling nanomachine has attractive application prospects in miRNA assay for biological researches and clinical diagnosis.
miRNAs 是一类内源性非编码 RNA,参与许多重要的生物学过程,已成为疾病治疗和诊断的一组新的生物标志物。探索高效的信号放大策略是追求高度敏感的 miRNA 生物传感平台的关键。DNA 纳米技术在放大 miRNA 生物传感器的制造方面显示出巨大的应用潜力。在这项工作中,开发了一种新型的 DNA 行走和滚动纳米机器,用于高度敏感和选择性地检测 miRNA。特别是,该方法通过相应的酶编程了两种形式的动力 DNA 纳米机器,这两种机器很好地集成在一起。它能够实现低至 39×10-18 m 的检测限,同时具有出色的抗干扰性能和临床应用。此外,通过设计 pH 控制的可分离的分子间 DNA 三聚体,可以方便地重置主要的传感元件,从而满足 miRNA 的即时护理分析的要求。所提出的方法与定量实时聚合酶链反应之间的高度一致性验证了其稳健性和可靠性。因此,预计 DNA 行走和滚动纳米机器在 miRNA 分析方面具有吸引力的应用前景,可用于生物学研究和临床诊断。