Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Anal Chem. 2024 Oct 22;96(42):16715-16723. doi: 10.1021/acs.analchem.4c03055. Epub 2024 Oct 11.
Herein, a novel functional DNA structure, acid-stimulated self-assembly DNA nanonetwork (ASDN), was proposed for miRNA-221 sensitive detection and high-resolution living cancer cell imaging. Significantly, the self-assembly of ASDN only occurred in the acidic extracellular environment of cancer cells, which could be endocytosed by cancer cells to eliminate the interference of noncancer cells and deliver the ASDN into cancer cells. Subsequently, endogenous miRNA-221 could trigger the catalytic hairpin assembly within ASDN, resulting in the separation of the fluorophore Cy5 and the quencher BHQ2 to recover the substantial Cy5 fluorescence signals, thus achieving signal amplification for sensitive detection of miRNA-221 with a detection limit of 5.5 pM, as well as facilitating high-resolution and low-background imaging of miRNA-221 in cancer cells. In consequence, this strategy provides an innovative DNA nanonetwork to distinguish cancer cells from other cells for sensitive detection of biomarkers, offering a meaningful reference for the application of DNA nanostructure self-assembly technology in relevant fundamental research and disease diagnosis.
在此,提出了一种新型的功能 DNA 结构,即酸刺激自组装 DNA 纳米网络(ASDN),用于 miRNA-221 敏感检测和高分辨率活癌细胞成像。重要的是,ASDN 的自组装仅在癌细胞的酸性细胞外环境中发生,这可以被癌细胞内吞,从而消除非癌细胞的干扰,并将 ASDN 递送到癌细胞内。随后,内源性的 miRNA-221 可以触发 ASDN 内的催化发夹组装,导致荧光团 Cy5 和猝灭剂 BHQ2 的分离,从而恢复大量的 Cy5 荧光信号,从而实现对 miRNA-221 的敏感检测,检测限为 5.5 pM,并且有利于在癌细胞中进行 miRNA-221 的高分辨率和低背景成像。因此,该策略提供了一种创新的 DNA 纳米网络,可用于区分癌细胞和其他细胞,以实现对生物标志物的敏感检测,为 DNA 纳米结构自组装技术在相关基础研究和疾病诊断中的应用提供了有意义的参考。