Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials, Ministry of Education, Shandong University, Jinan 250061, China.
Shenzhen Research Institute of Shandong University, Shenzhen 518057, China.
Biosensors (Basel). 2022 Jul 17;12(7):533. doi: 10.3390/bios12070533.
The detection of miRNA shows great promise in disease diagnosis. In this work, a ratiometric fluorescent biosensor based on multi-walled carbon nanotubes@gold nanoclusters (MWCNTs@Au NCs) and duplex-specific nuclease (DSN)-assisted signal amplification was fabricated for miRNA detection. Colorectal cancer (CRC)-associated miR-92a-3p extracted from exosomes was selected as the target. MWCNTs@Au NCs performs the dual functions of fluorescence quencher and internal fluorescence reference. In the absence of miR-92a-3p, an Atto-425-modified single-stranded DNA probe is adsorbed on MWCNTs@Au NCs, resulting in the quenching of Atto-425. In the presence of miR-92a-3p, the duplex is formed by hybridization of the probe and miR-92a-3p and leaves the MWCNTs@Au NCs, resulting in the fluorescence recovery of Atto-425. DSN can cleave the probe and result in the release of miR-92a-3p. The released miR-92a-3p can hybridize with other probes to form a signal amplification cycle. The fluorescence of MWCNTs@Au NCs remains stable and constitutes a ratiometric fluorescence system with that of Atto-425. A detection concentration interval of 0.1-10 pM and a limit of detection of 31 fM was obtained under optimized measurement conditions. In addition, the accuracy of the biosensor was validated by detecting the concentration of miR-92a-3p extracted from clinical exosome samples.
miRNA 的检测在疾病诊断中具有广阔的应用前景。本工作构建了一种基于多壁碳纳米管@gold 纳米簇(MWCNTs@Au NCs)和双链特异性核酸酶(DSN)辅助信号放大的比率荧光生物传感器,用于 miRNA 的检测。选择从外泌体中提取的结直肠癌(CRC)相关 miR-92a-3p 作为靶标。MWCNTs@Au NCs 具有荧光猝灭剂和内部荧光参比的双重功能。在没有 miR-92a-3p 的情况下,Atto-425 修饰的单链 DNA 探针被吸附在 MWCNTs@Au NCs 上,导致 Atto-425 荧光猝灭。当存在 miR-92a-3p 时,探针与 miR-92a-3p 杂交形成双链体,从而离开 MWCNTs@Au NCs,导致 Atto-425 的荧光恢复。DSN 可以切割探针并导致 miR-92a-3p 的释放。释放的 miR-92a-3p 可以与其他探针杂交,形成信号放大循环。MWCNTs@Au NCs 的荧光保持稳定,并与 Atto-425 的荧光构成比率荧光系统。在优化的测量条件下,获得了 0.1-10 pM 的检测浓度区间和 31 fM 的检测限。此外,通过检测从临床外泌体样本中提取的 miR-92a-3p 的浓度验证了生物传感器的准确性。