Department of Blood Transfusion, the Affiliated Hospital of Qingdao University, Qingdao, 266042, PR China; Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, Ministry of Education, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, 266042, PR China.
Department of Blood Transfusion, the Affiliated Hospital of Qingdao University, Qingdao, 266042, PR China.
Anal Chim Acta. 2024 Oct 2;1324:343103. doi: 10.1016/j.aca.2024.343103. Epub 2024 Aug 13.
Recently, various techniques have been developed to accurately and sensitively detect tumor biomarkers for the early diagnosis and effective therapy of cancer. The electrochemiluminescence (ECL) method holding outstanding features including high sensitivity, ease of operation, and spatiotemporal controllability exhibited great potential for DNA/RNA detection, immunoassay, cancer cell detection, and environmental analysis. However, a glaring problem of ECL approaches is that the layer-by-layer modification on the electrode leads to poor stability and sensitivity of the sensors. Therefore, new simple and efficient methods for electrode modification which can effectively improve the ECL signal have attracted more and more research interests.
Based on the dual amplification strategy of target-induced CHA and nanocomposite probes leading to self-generated co-reactant (HO), we proposed a highly sensitive miRNA-ECL detection system. The introduction of the target miRNA-21 triggers the CHA cycle amplification of DNA1 and biotin-modified DNA2, releasing the target miRNA-21 sequence for the target cycle reaction. After the reaction, the newly introduced DNA2 was combined with Au NPs modified with SA and Glucose oxidase (GOD). In the presence of oxygen, glucose was decomposed by GOD to produce HO, and then HO was immediately catalyzed by the Hemin/G-quadruplex at the double-stranded end of the CHA product to produce a large amount of O. As a co-reactant of luminol, the ECL signal was significantly enhanced, thereby achieving highly sensitive detection of miRNA-21 content and obtaining a low detection limit of 0.65 fM. The high specificity of the ECL biosensor was also proved by base mismatch.
Compared with other current detection methods, this sensor can achieve quantitative analysis of other target analytes by flexibly changing the probe DNA sequence, and provide a new feasible solution for the detection of tumor-associated markers. Benefiting from the improved sensitivity and selectivity, the proposed biosensing platform is expected to provide a new strategy for biomarkers analysis and outstanding prospect for further clinical application.
最近,已经开发出各种技术来准确、灵敏地检测肿瘤生物标志物,以实现癌症的早期诊断和有效治疗。电化学发光(ECL)法具有高灵敏度、操作简便、时空可控性等突出特点,在 DNA/RNA 检测、免疫分析、癌细胞检测和环境分析等方面具有很大的应用潜力。然而,ECL 方法的一个明显问题是,电极的逐层修饰导致传感器的稳定性和灵敏度较差。因此,新的简单有效的电极修饰方法,能有效提高 ECL 信号,引起了越来越多的研究兴趣。
基于目标诱导 CHA 和纳米复合探针引发自生成共反应物(HO)的双重扩增策略,我们提出了一种高灵敏的 miRNA-ECL 检测系统。引入靶 miRNA-21 触发 DNA1 和生物素修饰的 DNA2 的 CHA 循环扩增,释放靶 miRNA-21 序列进行靶循环反应。反应后,新引入的 DNA2 与 SA 和葡萄糖氧化酶(GOD)修饰的 Au NPs 结合。在氧气存在下,GOD 分解葡萄糖产生 HO,然后 HO 立即被 CHA 产物双链末端的血红素/G-四链体催化产生大量 O。作为鲁米诺的共反应物,ECL 信号显著增强,从而实现了对 miRNA-21 含量的高灵敏度检测,检测限低至 0.65 fM。ECL 生物传感器的高特异性也通过碱基错配得到了证明。
与其他当前的检测方法相比,通过灵活改变探针 DNA 序列,该传感器可以实现其他目标分析物的定量分析,并为肿瘤相关标志物的检测提供新的可行解决方案。得益于提高的灵敏度和选择性,所提出的生物传感平台有望为生物标志物分析提供新的策略,并为进一步的临床应用提供广阔的前景。