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尺寸分辨 DNA 纳米笼框架实现活细胞中成熟 microRNA 的灵敏和高保真成像。

Size-Discriminative DNA Nanocage Framework Enables Sensitive and High-Fidelity Imaging of Mature MicroRNA in Living Cells.

机构信息

Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, P. R. China.

出版信息

Anal Chem. 2022 Jul 12;94(27):9927-9933. doi: 10.1021/acs.analchem.2c02026. Epub 2022 Jun 24.

Abstract

Mature microRNAs (miRNAs) are closely associated with cell proliferation and differentiation, stress response, and carcinogenesis, and monitoring intracellular miRNAs can contribute to the studies of their regulatory roles and molecular mechanisms of disease progression. However, accurate and reliable detection of mature miRNAs in complex physiological environments encounters the challenge of undesired detection accuracy ascribed to the coexistence of their precursor microRNAs (pre-miRNAs) and degradation of sensing probes. Here, we demonstrate the synthesis of a new size-discriminative DNA nanocage framework (DNF) for the sensitive monitoring of mature miRNA-21 in living cells with high accuracy via cascaded toehold-mediated strand displacement reaction (TSDR) amplifications. The DNF is prepared by a simple self-assembly of six ssDNAs, and the signal probes are docked inside the DNF. Because of its rigid framework structure, the DNF shows enhanced enzyme stability. Upon entering cells, only the short target mature miRNA-21 sequences instead of the large-sized pre-miRNAs are allowed to be accommodated inside the cavity of the DNF owing to the size-discriminative capability of the DNF. The cascaded TSDR amplifications can thus be activated by the mature miRNA-21 together with endogenous ATP to result in magnified fluorescence for sensitive detection and selective discrimination of miRNA-21 from the interference pre-miRNAs. Our results indicate that the DNF probes can offer robust sensing means for detecting various intracellular mature miRNAs with high accuracy for disease diagnoses and biomedical studies.

摘要

成熟的 microRNAs(miRNAs)与细胞增殖和分化、应激反应和致癌作用密切相关,监测细胞内的 miRNAs 有助于研究它们的调控作用和疾病进展的分子机制。然而,在复杂的生理环境中准确可靠地检测成熟的 miRNAs 面临着一个挑战,即由于其前体 microRNAs(pre-miRNAs)的共存和传感探针的降解,检测精度不理想。在这里,我们展示了一种新的大小区分性 DNA 纳米笼框架(DNF)的合成,用于通过级联的引发物介导链置换反应(TSDR)扩增,以高精度灵敏监测活细胞中的成熟 miRNA-21。DNF 通过 6 个 ssDNA 的简单自组装制备,信号探针被对接在 DNF 内部。由于其刚性框架结构,DNF 显示出增强的酶稳定性。进入细胞后,由于 DNF 的尺寸区分能力,只有短的目标成熟 miRNA-21 序列而不是大尺寸的 pre-miRNAs 被允许容纳在 DNF 的腔体内。级联的 TSDR 扩增可以被成熟的 miRNA-21 与内源性 ATP 一起激活,从而产生放大的荧光,用于灵敏检测和选择性区分 miRNA-21 与干扰的 pre-miRNAs。我们的结果表明,DNF 探针可以为疾病诊断和生物医学研究中检测各种细胞内成熟 miRNAs 提供稳健的传感手段,具有高精度。

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