School of Pharmacy, Nanjing Medical University, Nanjing, 211166, PR China.
School of Pharmacy, Nanjing Medical University, Nanjing, 211166, PR China.
Anal Chim Acta. 2019 Jan 24;1047:21-27. doi: 10.1016/j.aca.2018.09.040. Epub 2018 Sep 19.
Herein, a novel magnetic biocomposite (FeO@Au-S1/S2) was applied to analyze thrombin. The FeO@Au-S1/S2 consisted of FeO@Au nanoparticles (FeO@Au NPs) as carriers for magnetic separation and magnetic field-induced self-assembly, thiolated complementary strand (S1) anchored based on Au-S bond and thrombin binding aptamer (S2) as a recognition element. As a redox indicator, methylene blue (MB) can be adsorbed to DNA anchored on the surface of FeO@Au NPs by electro-static interaction. In the absence of thrombin, MB were adsorbed on double-stranded DNA (S1/S2) which anchored on FeO@Au NPs and a high electrochemical signal of MB was recorded by Differential pulse voltammetry. Conversely, the complementary strand (S1) exposed after thrombin competitively bonded with aptamer. The introduction of Pb-dependent DNAzyme (S3) split S1 at specific rA site, resulting in the significantly decreased adsorption capacity of MB. Thus, the thrombin detection could be recorded by monitoring the electrochemical signal reduction of MB through incubation of thrombin with S3. This method exhibited a high sensitivity toward thrombin with a broad linear range from 5 pmol L to 5 nmol L and a limit of detection of 1.8 pmol L.
本文应用一种新型的磁性生物复合材料(FeO@Au-S1/S2)来分析凝血酶。FeO@Au-S1/S2 由 FeO@Au 纳米粒子(FeO@Au NPs)作为载体,用于磁分离和磁场诱导的自组装,基于 Au-S 键的巯基化互补链(S1)和凝血酶结合适体(S2)作为识别元件。作为一种氧化还原指示剂,亚甲基蓝(MB)可以通过静电相互作用吸附到固定在 FeO@Au NPs 表面的 DNA 上。在没有凝血酶的情况下,MB 被吸附到双链 DNA(S1/S2)上,该双链 DNA 固定在 FeO@Au NPs 上,并通过差分脉冲伏安法记录 MB 的高电化学信号。相反,在凝血酶竞争结合适体后,互补链(S1)暴露出来。Pb 依赖性 DNA 酶(S3)在特定的 rA 位点切开 S1,导致 MB 的吸附容量显著降低。因此,通过孵育凝血酶与 S3,可以通过监测 MB 的电化学信号还原来记录凝血酶的检测。该方法对凝血酶具有高灵敏度,线性范围从 5 pmol L 到 5 nmol L,检测限为 1.8 pmol L。