Ito Toshiyuki, Hosokawa Kazuo, Maeda Mizuo
Bioengineering Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Biosens Bioelectron. 2007 Mar 15;22(8):1816-9. doi: 10.1016/j.bios.2006.08.008. Epub 2006 Sep 18.
Herein, we report an anomalous electrochemical behavior of surface-bound DNA duplex that has single-base mismatches at its distal end. Single-stranded 15-base DNA was immobilized at its 5'end onto gold electrode surfaces. After hybridization with complementary or mismatched DNA, electrochemical impedance spectra were obtained using [Fe(CN)(6)]3-/4- as redox marker ions. Hybridization with the complementary DNA reduced the charge-transfer resistance (R(CT)), whereas single-base mismatches at the distal end of the duplex largely increased the R(CT). This anomaly was found only with the distal end: the increase in R(CT) was not observed for mismatches at either the middle or the proximal end. These results indicate that electrochemical detection of single-base alterations at an end of sample DNA is exceptionally easy because of the diametrically opposite responses. This detection principle is promising for the typing of single-nucleotide polymorphisms in combination with the single-base primer extension protocol.
在此,我们报告了一种表面结合的DNA双链体的异常电化学行为,该双链体在其远端存在单碱基错配。15个碱基的单链DNA在其5'端固定在金电极表面。与互补或错配的DNA杂交后,使用[Fe(CN)₆]³⁻/⁴⁻作为氧化还原标记离子获得电化学阻抗谱。与互补DNA杂交降低了电荷转移电阻(R(CT)),而双链体远端的单碱基错配则大大增加了R(CT)。这种异常仅在远端出现:在中间或近端的错配未观察到R(CT)增加。这些结果表明,由于完全相反的响应,对样品DNA一端的单碱基改变进行电化学检测异常容易。这种检测原理与单碱基引物延伸方案相结合,在单核苷酸多态性分型方面很有前景。