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一种高效的基于局部催化发夹组装的 DNA 纳米机器,用于活细胞中 miRNA-21 的成像。

An efficient localized catalytic hairpin assembly-based DNA nanomachine for miRNA-21 imaging in living cells.

机构信息

Research Center of Analytical Instrumentation, Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710069, Shaanxi, P.R. China.

出版信息

Analyst. 2021 May 4;146(9):3041-3051. doi: 10.1039/d1an00001b.

Abstract

As an enzyme-free isothermal amplification strategy, catalytic hairpin assembly (CHA) is a very promising method for cell imaging. However, the practical application of CHA on intracellular miRNA imaging is limited by slow kinetics, insufficient amplification efficiency and strong interference in living cells. Herein, a localized catalytic hairpin assembly-based DNA nanomachine (LCHA nanomachine) was developed for the rapid, efficient and reliable fluorescence resonance energy transformation (FRET) imaging of miRNA-21 in living cells. The nanomachine was simply constructed by a one-step self-assembly process of a stator strand, a pair of hairpin probes from CHA and an AS1411 aptamer. Benefiting from the spatial-confinement effect, a pair of hairpin probes with high collision frequency was rapidly and efficiently assembled using miRNA-21 as the catalyst on a stator strand in every nanomachine. Compared with the free-CHA nanomachine, the LCHA nanomachine shortened the reaction time by 4.5-fold for reaching a plateau and significant improved the sensitivity by 7.6-fold for miRNA-21 detection in vitro. Importantly, the nanomachine was successfully applied for miRNA-21 imaging in living cells. With the assistance of an AS1411 aptamer and stator strand, the pair of hairpin probes with the ratio of 1 : 1 synchronously transported into a co-site of the cytoplasm, which ensures efficient imaging of trace miRNA-21. The signal output of the ratio of 6-carboxy-fluorescein (FAM) to tetramethyl rhodamine (TAMRA) intensities guaranteed reliability through avoiding the interference from different amounts of the nanomachine that enters into cells. Notably, the nanomachine can distinguish the miRNA-21 expression level in different kinds of cancer cells. By virtue of the advantages of simplicity, efficiency and reliability, the proposed strategy provides a powerful method for exploring the functions of miRNA and diagnosis of disease.

摘要

作为一种无需酶的等温扩增策略,催化发夹组装(CHA)是一种非常有前途的细胞成像方法。然而,CHA 在细胞内 miRNA 成像中的实际应用受到动力学缓慢、扩增效率不足和活细胞中强干扰的限制。在此,开发了一种基于局部催化发夹组装的 DNA 纳米机器(LCHA 纳米机器),用于在活细胞中快速、高效和可靠地荧光共振能量转移(FRET)成像 miRNA-21。纳米机器通过定子链、CHA 的一对发夹探针和 AS1411 适体的一步自组装过程简单构建。受益于空间限制效应,每一个纳米机器中,miRNA-21 作为催化剂,一对发夹探针以高碰撞频率快速高效地组装在定子链上。与游离 CHA 纳米机器相比,LCHA 纳米机器将达到平台所需的反应时间缩短了 4.5 倍,体外检测 miRNA-21 的灵敏度提高了 7.6 倍。重要的是,该纳米机器成功应用于活细胞中的 miRNA-21 成像。在 AS1411 适体和定子链的辅助下,比例为 1:1 的一对发夹探针同步运送到细胞质的共位点,从而确保了痕量 miRNA-21 的高效成像。通过避免不同量的纳米机器进入细胞而产生的干扰,FAM 和 TAMRA 强度比的信号输出保证了可靠性。值得注意的是,该纳米机器可以区分不同类型癌细胞中的 miRNA-21 表达水平。该策略凭借其简单、高效和可靠的优势,为探索 miRNA 的功能和疾病诊断提供了一种强大的方法。

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