Orderly Aggregated Catalytic Hairpin Assembly for Synchronous Ultrasensitive Detecting and High-Efficiency Co-Localization Imaging of Dual-miRNAs in Living Cells

化学 共域化 小RNA 荧光寿命成像显微镜 荧光 生物物理学 DNA 滚动圆复制 环介导等温扩增 纳米技术 猝灭(荧光) 细胞生物学 DNA复制 生物化学 物理 基因 光学 材料科学 生物
作者
Jie Zhou,Fang Liu,Yichen Han,Hongling Li,Shaping Wei,Yu Ouyang,Yaqin Chai,Ruo Yuan
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:95 (39): 14558-14565 被引量:6
标识
DOI:10.1021/acs.analchem.3c01764
摘要

In this work, the orderly aggregated catalytic hairpin assembly (OA-CHA) was developed for synchronous ultrasensitive detection and high-efficiency colocalization imaging of dual-miRNAs by a carefully designed tetrahedral conjugated ladder DNA structure (TCLDS). Exactly, two diverse hairpin probes were fixed on tetrahedron conjugated DNA nanowires to form the TCLDS without fluorescence response, which triggered OA-CHA in the aid of output DNA 1 and output DNA 2 produced by targets miRNA-217 and miRNA-196a cycle to generate TCLDS with remarkable fluorescence response. Impressively, compared with the traditional CHA strategy, OA-CHA avoided the fluorescence group and quenching group from approaching again because of the spatial confinement effect to significantly enhance the fluorescence signal, resulting in the simultaneous ultrasensitive detection of dual-miRNAs with detection limits of 21 and 32 fM for miRNA-217 and miRNA-196a, respectively. Meanwhile, the TCLDS with lower diffusivity could achieve accurate localization imaging for reflecting the spatial distribution of dual-miRNAs in living cells. The strategy based on OA-CHA provided a flexible and programmable nucleic amplification method for the synchronous ultrasensitive detection and precise imaging of multiple biomarkers and had potential in disease diagnostics..
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