Department of Chemistry, Faculty of Science, University of Isfahan, Isfahan 81746-73441, Iran.
Biosens Bioelectron. 2011 Jul 15;26(11):4308-13. doi: 10.1016/j.bios.2011.04.020. Epub 2011 Apr 16.
In this manuscript, a strategy for the amplification of the responses of an electrochemical DNA hybridization biosensor using silver nanoparticles (Ag-NPs) as redox reporters and its capability for the detection of a single base mismatches (SBM) including thermodynamically stable ones, is described. In this assay, Ag-NPs are immobilized on the top of recognition layer and their oxidation signals are followed. Differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS) are used to monitoring the electrode response. Only for complementary target sequence, electron can transfer between Electrode surface and nanoparticles via DNA and Ag-NPs can be oxidized. Therefore this DNA biosensor could differentiate between complementary target and one containing either SBM or thermodynamically stable G-A and G-T targets through oxidation signal of Ag-NPs. This biosensor is able to detect SBM by overcome the direct electron transfer of redox reporter with electrode surface and positioning of it before the mismatch position.
在本文中,描述了一种使用银纳米粒子 (Ag-NPs) 作为氧化还原报告分子来放大电化学 DNA 杂交生物传感器响应的策略,以及该策略用于检测包括热力学稳定的单碱基错配 (SBM) 的能力。在该测定中,Ag-NPs 固定在识别层的顶部,并跟踪其氧化信号。差分脉冲伏安法 (DPV) 和电化学阻抗谱 (EIS) 用于监测电极响应。只有对于互补的靶序列,电子才能通过 DNA 在电极表面和纳米粒子之间传递,并且 Ag-NPs 可以被氧化。因此,通过 Ag-NPs 的氧化信号,这种 DNA 生物传感器可以区分互补的靶序列和含有单碱基错配或热力学稳定的 G-A 和 G-T 靶序列的靶序列。该生物传感器能够通过克服氧化还原报告分子与电极表面的直接电子转移并将其定位在错配位置之前来检测 SBM。