Key Laboratory of the Environmental Medicine and Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing 210009, China.
School of Medicine, Southeast University, Nanjing 210009, China.
Int J Biol Macromol. 2022 Dec 1;222(Pt A):794-802. doi: 10.1016/j.ijbiomac.2022.09.182. Epub 2022 Sep 26.
Amyloid-β oligomers (AβOs) was the core-biomarker of Alzheimer's disease (AD), and the detection of AβOs is very important for the early diagnosis of AD. However, existing tests for AβOs are majorly suffering from complex process and poor sensitivity. Thus, an adjustable AβOs electrochemiluminescence (ECL) aptasensor based on the synergistic effect of self-enhanced metal-organic gel (AgCNS) and triple-helix DNA system (THS) was successfully constructed. AgCNS was prepared by an extremely simple one-pot method and was an innovative luminophore with excellent ECL performance. The AgCNS-labeled complementary sequence (AgCNS@CP) was interlaced with the unlabeled aptamer (Apt) carrying two short-arms fixed on the gold electrode (GE) to form the THS. Along with the specific-binding of AβOs and Apt, the THS was disrupted and adjusted flexibly between "on" and "off", resulting in significant changes in the ECL signals. Thus, ECL detection of AβOs was sensitively achieved with a detection limit as low as 0.23 fM and the different forms of Aβ can be specifically distinguished. The aptasensor also exhibited satisfactory selectivity, stability and reproducibility. Moreover, when proposed method and ELISA-kit were simultaneously applied to artificial cerebrospinal fluid (A-CSF) samples, the obtained results were completely consistent, reflecting the potential clinical application value of this work.
淀粉样蛋白-β 寡聚体 (AβOs) 是阿尔茨海默病 (AD) 的核心生物标志物,检测 AβOs 对于 AD 的早期诊断非常重要。然而,现有的 AβOs 检测方法主要存在过程复杂和灵敏度差的问题。因此,成功构建了一种基于自增强金属有机凝胶 (AgCNS) 和三螺旋 DNA 系统 (THS) 协同作用的可调 AβOs 电化学发光 (ECL) 适体传感器。AgCNS 通过极其简单的一锅法制备,是一种具有优异 ECL 性能的创新发光体。AgCNS 标记的互补序列 (AgCNS@CP) 与带有两条固定在金电极 (GE) 上的短臂的未标记适体 (Apt) 交错形成 THS。随着 AβOs 和 Apt 的特异性结合,THS 被灵活地打开和关闭,导致 ECL 信号发生显著变化。因此,通过灵敏地检测 AβOs,实现了检测限低至 0.23 fM 的 ECL 检测,并且可以特异性区分不同形式的 Aβ。该适体传感器还表现出令人满意的选择性、稳定性和重现性。此外,当将该方法和 ELISA 试剂盒同时应用于人工脑脊液 (A-CSF) 样本时,获得的结果完全一致,反映了这项工作的潜在临床应用价值。