Liu Jia-Li, Yang Yu-Ting, Jin Yu-Shuang, Zhou Ying, Shen Zhao-Chen, Chai Ya-Qin, Yuan Ruo
College of Sericulture, Textile and Biomass Science, State Key Lab Resource Insects, Southwest University, Chongqing, 400715, PR China; 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.
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.
Biosens Bioelectron. 2025 Oct 15;286:117555. doi: 10.1016/j.bios.2025.117555. Epub 2025 May 23.
Herein, silver-doped cadmium telluride quantum dots (Ag-CdTe QDs) as electrochemiluminescence (ECL) emitter with intense ECL signal and hairpin-fueled entropy-driven reactions (H-EDR) as signal amplifier with high conversion efficiency and low signal leakage were exploited to construct an ECL biosensor for ultrasensitive determination of microRNA 222 (miRNA-222) related to liver cancer. Interestingly, the ECL intensity of Ag-CdTe QDs has been improved by 2.5 times compared to that of undoped CdTe QDs for improving the detection sensitivity, which attributed to the crystal shape transformation of Ag-CdTe QDs through silver doping for the reduction of band gap to change the electron-hole recombination path. Moreover, H-EDR could reduce the background signal by introducing a hairpin DNA module rather than a linear DNA single strand as a fuel strand to conquer the undesired signal leakage deriving from the dynamic breathing of the DNA components, which achieved the target conversion from trace miRNA-222 to abundant output DNA for further enhancing the detection sensitivity. Thus, the developed ECL biosensor realizes the sensitive detection of miRNA-222 with a detection limit of 44 aM (aM), which was further applied in miRNA-222 analysis of cancer cell (MHCC-97L, a human hepatocellular carcinoma cell line and HeLa, a cervical cancer cell line) lysate. This work proposed a sensitive strategy by improving the ECL signal of the developed CdTe QDs and reducing the background signal during the target amplification process, which was expected to detect trace biomarkers for early clinical testing and disease monitoring.
在此,以具有强电化学发光(ECL)信号的银掺杂碲化镉量子点(Ag-CdTe QDs)作为ECL发光体,以具有高转换效率和低信号泄漏的发夹驱动熵驱动反应(H-EDR)作为信号放大器,构建了一种用于超灵敏检测与肝癌相关的微小RNA 222(miRNA-222)的ECL生物传感器。有趣的是,与未掺杂的CdTe QDs相比,Ag-CdTe QDs的ECL强度提高了2.5倍,以提高检测灵敏度,这归因于通过银掺杂使Ag-CdTe QDs的晶体形状转变,从而减小带隙以改变电子-空穴复合路径。此外,H-EDR可以通过引入发夹DNA模块而不是线性DNA单链作为燃料链来降低背景信号,以克服由于DNA组件的动态呼吸引起的不期望的信号泄漏,从而实现从痕量miRNA-222到大量输出DNA的目标转换,进一步提高检测灵敏度。因此,所开发的ECL生物传感器实现了对miRNA-222的灵敏检测,检测限为44阿摩尔(aM),并进一步应用于癌细胞(MHCC-97L,一种人肝癌细胞系和HeLa,一种宫颈癌细胞系)裂解物的miRNA-222分析。这项工作通过改善所开发的CdTe QDs的ECL信号并在目标扩增过程中降低背景信号,提出了一种灵敏的策略,有望用于早期临床检测和疾病监测中的痕量生物标志物检测。