The Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, PR China.
Biosens Bioelectron. 2010 Feb 15;25(6):1290-4. doi: 10.1016/j.bios.2009.10.017. Epub 2009 Oct 21.
A novel electrochemical assay based on the aptamer and the signal of amplification of nanoparticles (NPs) was constructed for the determination of thrombin. Aptamers immobilized on the electrode and Au NPs could be assembled with the target protein to form a sandwich structure in the presence of the latter. Differential pulse voltammetry (DPV) was employed to detect the CdS NPs loaded on the surface of the Au NPs through the linker DNA, which was related to the concentration of the target protein. The assay took advantage of the amplification ability of Au nanoparticles carrying multiplex CdS NPs and the specific affinity of aptamers. Thrombin was detected in this assay in the linear range of 1.0x10(-15) to 1.0x10(-11) M with the detection limit of 5.5x10(-16) M of target protein. In addition, the assay could be used to detection thrombin in real samples with high sensitivity and good selectivity.
基于适体和纳米粒子(NPs)信号放大的新型电化学分析方法被构建用于凝血酶的测定。将适体固定在电极上,Au NPs 可以在存在目标蛋白的情况下与目标蛋白组装形成三明治结构。通过连接 DNA 检测负载在 Au NPs 表面的 CdS NPs 的差分脉冲伏安法(DPV),这与目标蛋白的浓度有关。该测定利用了携带多重 CdS NPs 的 Au 纳米粒子的放大能力和适体的特异性亲和力。在该测定中,凝血酶在 1.0x10(-15) 到 1.0x10(-11) M 的线性范围内被检测到,目标蛋白的检测限为 5.5x10(-16) M。此外,该测定方法可用于高灵敏度和良好选择性地检测真实样品中的凝血酶。