Department of Chemistry and Chemical Engineering, Xinxiang University, Xinxiang 453000, PR China.
Southwest Hospital & Institute of Hepatobilitary Surgery, the Third Military Medical University, Chongqing 400038, PR China; Department of General Surgery, the 371th Hospital of PLA, Xinxiang 453000, PR China.
Biosens Bioelectron. 2014 Jul 15;57:16-21. doi: 10.1016/j.bios.2014.01.040. Epub 2014 Jan 31.
For the first time, a sensitive electrochemical aptasensor for thrombin (TB) was developed by using porous platinum nanotubes (PtNTs) labeled with hemin/G-quadruplex and glucose dehydrogenase (GDH) as labels. Porous PtNTs with large surface area exhibited the peroxidase-like activity. Coupling with GDH and hemin/G-quadruplex as NADH oxidase and HRP-mimicking DNAzyme, the cascade signal amplification was achieved by the following ways: in the presence of glucose and NAD(+) in the working buffer, GDH electrocatalyzed the oxidation of glucose with the production of NADH. Then, hemin/G-quadruplex as NADH oxidase catalyzed the oxidation of NADH to in situ generate H2O2. Based on the corporate electrocatalysis of PtNTs and hemin/G-quadruplex toward H2O2, the electrochemical signal was significantly amplified, allowing the detection limit of TB down to 0.15 pM level. Moreover, the proposed strategy was simple because the intercalated hemin offered the readout signal, avoiding the adding of additional redox mediator as signal donator. Such an electrochemical aptasensor is highly promising for sensitive detection of other proteins in clinical diagnostics.
首次开发了一种基于多孔铂纳米管(PtNTs)标记血红素/G-四链体和葡萄糖脱氢酶(GDH)的凝血酶(TB)敏感电化学适体传感器。具有大表面积的多孔 PtNTs 表现出过氧化物酶样活性。与 GDH 和血红素/G-四链体作为 NADH 氧化酶和 HRP 模拟 DNA 酶结合,通过以下方式实现级联信号放大:在工作缓冲液中存在葡萄糖和 NAD(+)的情况下,GDH 电催化葡萄糖氧化,生成 NADH。然后,血红素/G-四链体作为 NADH 氧化酶,将 NADH 氧化为原位生成 H2O2。基于 PtNTs 和血红素/G-四链体对 H2O2 的协同电催化作用,电化学信号得到显著放大,使 TB 的检测限低至 0.15 pM 水平。此外,该策略简单,因为嵌入的血红素提供了读出信号,避免了添加额外的氧化还原介体作为信号供体。这种电化学适体传感器在临床诊断中用于灵敏检测其他蛋白质具有广阔的应用前景。