Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, and Chongqing Engineering Laboratory of Nanomaterials & Sensor Technologies, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, P. R. China.
Anal Chem. 2024 Jun 4;96(22):9097-9103. doi: 10.1021/acs.analchem.4c00664. Epub 2024 May 20.
Herein, a fluorescence light-up 3D DNA walker (FLDW) was powered and accelerated by endogenous adenosine-5'-triphosphate (ATP) molecules to construct a biosensor for sensitive and rapid label-free detection and imaging of microRNA-221 (miRNA-221) in malignant tumor cells. Impressively, ATP as the driving force and accelerator for FLDW could significantly accelerate the operation rate of FLDW, reduce the likelihood of errors in signaling, and improve the sensitivity of detection and imaging. When FLDW was initiated by output DNA H1-op transformed by target miRNA-221, G-rich sequences in the S strand, anchored to AuNP, were exposed to form G-quadruplexes (G4s), and thioflavin T (ThT) embedded in the G4s emitted intense fluorescence to realize sensitive and rapid detection of target miRNA-221. Meanwhile, the specific binding of ThT to G4 with a weak background fluorescence response was utilized to enhance the signal-to-noise ratio of the label-free assay straightforwardly and cost-effectively. The proposed FLDW system could realize sensitive detection of the target miRNA-221 in the range of 1 pM to 10 nM with a detection limit of 0.19 pM by employing catalytic hairpin assembly (CHA) to improve the conversion of the target. Furthermore, by harnessing the abundant ATP present in the tumor microenvironment, FLDW achieved rapid and accurate imaging of miRNA-221 in cancer cells. This strategy provides an innovative and high-speed label-free approach for the detection and imaging of biomarkers in cancer cells and is expected to be a powerful tool for bioanalysis, diagnosis, and prognosis of human diseases.
在此,我们构建了一个由内源性三磷酸腺苷(ATP)分子驱动和加速的荧光点亮三维 DNA walker(FLDW),用于构建一个生物传感器,用于灵敏、快速地检测和成像恶性肿瘤细胞中的 microRNA-221(miRNA-221)。令人印象深刻的是,作为 FLDW 的驱动力和加速剂的 ATP 可以显著提高 FLDW 的运行速度,降低信号错误的可能性,并提高检测和成像的灵敏度。当 FLDW 被由目标 miRNA-221 转化的输出 DNA H1-op 启动时,与 AuNP 锚定的 S 链中的 G 丰富序列被暴露,形成 G-四链体(G4s),嵌入 G4s 中的硫黄素 T(ThT)发出强烈的荧光,实现对目标 miRNA-221 的灵敏、快速检测。同时,利用 ThT 与背景荧光响应较弱的 G4 的特异性结合,直接且经济有效地增强了无标记测定的信号与噪声比。该提出的 FLDW 系统可以通过采用催化发夹组装(CHA)来提高目标的转化率,实现对目标 miRNA-221 的灵敏检测,检测范围为 1 pM 至 10 nM,检测限为 0.19 pM。此外,通过利用肿瘤微环境中丰富的 ATP,FLDW 可以快速、准确地对癌细胞中的 miRNA-221 进行成像。该策略为癌细胞中生物标志物的检测和成像提供了一种创新的、高速的无标记方法,有望成为生物分析、诊断和人类疾病预后的有力工具。