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.
Anal Chem. 2024 Aug 20;96(33):13644-13651. doi: 10.1021/acs.analchem.4c02529. Epub 2024 Aug 7.
Intracellular detection and imaging of microRNAs (miRNAs) with low expression usually face the problem of unsatisfactory sensitivity. Herein, a novel dual-function DNA nanowire (DDN) with self-feedback amplification and efficient signal transduction was developed for the sensitive detection and intracellular imaging of microRNA-155 (miRNA-155). Target miRNA-155 triggered catalytic hairpin assembly (CHA) to generate plenty of double-stranded DNA (dsDNA), and a trigger primer exposed in dsDNA initiated a hybridization chain reaction (HCR) between four well-designed hairpins to produce DDN, which was encoded with massive target sequences and DNAzyme. On the one hand, target sequences in DDN acted as self-feedback amplifiers to reactivate cascaded CHA and HCR, achieving exponential signal amplification. On the other hand, DNAzyme encoded in DDN acted as signal transducers, successively cleaving Cy5 and BHQ-2 labeled substrate S to obtain a significantly enhanced fluorescence signal. This efficient signal transduction coupling self-feedback amplification greatly improved the detection sensitivity with a limit of detection of 160 aM for miRNA-155, enabling ultrasensitive imaging of low-abundance miRNA-155 in living cells. The constructed DDN creates a promising fluorescence detection and intracellular imaging platform for low-expressed biomarkers, exhibiting tremendous potential in biomedical studies and clinical diagnosis of diseases.
用低表达的方法对 microRNAs (miRNAs) 进行细胞内检测和成像通常会面临灵敏度不理想的问题。在此,开发了一种具有自反馈放大和高效信号转导功能的新型双功能 DNA 纳米线(DDN),用于 microRNA-155 (miRNA-155) 的灵敏检测和细胞内成像。靶 miRNA-155 触发催化发夹组装 (CHA) 以产生大量双链 DNA (dsDNA),并且在 dsDNA 中暴露的触发引物启动了四个精心设计的发夹之间的杂交链式反应 (HCR),以产生 DDN,其编码了大量的靶序列和 DNA 酶。一方面,DDN 中的靶序列充当自反馈放大器,重新激活级联 CHA 和 HCR,实现指数信号放大。另一方面,DDN 中编码的 DNA 酶充当信号转导器,依次切割 Cy5 和 BHQ-2 标记的底物 S,以获得显著增强的荧光信号。这种高效的信号转导与自反馈放大相结合,大大提高了检测灵敏度,对 miRNA-155 的检测限低至 160 aM,实现了对低丰度 miRNA-155 的超灵敏细胞内成像。所构建的 DDN 为低表达生物标志物的荧光检测和细胞内成像创建了一个很有前景的平台,在生物医学研究和疾病的临床诊断中具有巨大的潜力。