Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, P. R. China.
The Institute of Chemistry, Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
Anal Chem. 2023 Aug 29;95(34):12754-12760. doi: 10.1021/acs.analchem.3c01470. Epub 2023 Aug 17.
In this study, a pH-stimulated self-locked DNA nanostructure (SLDN) was developed to efficiently distinguish cancer cells from other cells for the simultaneous detection and imaging of endogenous dual-microRNAs (miRNAs). Impressively, the SLDN was specifically unlocked in the acidic environment of cancer cells to form unlocked-SLDN to disengage the i-motif sequence with a labeled fluorophore for the recovery of a fluorescence signal, resulting in the differentiation of cancer cells from normal cells. Meanwhile, unlocked-SLDN could combine and recognize the targets miRNA-21 and miRNA-155 simultaneously to trigger the hybridization chain reaction (HCR) amplification for sensitive dual-miRNA detection, with detection limits of 1.46 pM for miRNA-21 and 0.72 pM for miRNA-155. Significantly, compared with the current miRNA imaging strategy based on the traditional DNA nanostructure, the strategy proposed here remarkably eliminates the interference of normal cells to achieve high-resolution colocation imaging of miRNAs in tumor cells with an ultralow background signal. This work provided a specific differentiation method for tumor cells to materialize sensitive biomarker detection and distinguishable high-definition live-cell imaging for precise cancer diagnosis and multifactor research of tumor progression.
在这项研究中,开发了一种 pH 刺激的自锁定 DNA 纳米结构(SLDN),可有效地将癌细胞与其他细胞区分开来,用于内源性双重 microRNA(miRNA)的同时检测和成像。令人印象深刻的是,SLDN 仅在癌细胞的酸性环境中特异性解锁,形成解锁-SLDN,以释放与标记荧光团的 i 型序列结合,恢复荧光信号,从而将癌细胞与正常细胞区分开来。同时,解锁-SLDN 可以结合并识别靶 miRNA-21 和 miRNA-155,同时触发杂交链式反应(HCR)扩增,实现敏感的双重 miRNA 检测,miRNA-21 的检测限为 1.46 pM,miRNA-155 的检测限为 0.72 pM。重要的是,与基于传统 DNA 纳米结构的当前 miRNA 成像策略相比,这里提出的策略可以显著消除正常细胞的干扰,实现肿瘤细胞中 miRNA 的高分辨率共定位成像,具有超低背景信号。这项工作为肿瘤细胞提供了一种特定的分化方法,实现了对生物标志物的敏感检测和对肿瘤进展的多因素研究的可区分的高清活细胞成像,以实现精确的癌症诊断。