首页> 外文期刊>Analytica chimica acta >Electrochemical detection of DNA hybridization based on silver-enhanced gold nanoparticle label
【24h】

Electrochemical detection of DNA hybridization based on silver-enhanced gold nanoparticle label

机译:基于银增强金纳米颗粒标记的DNA杂交电化学检测

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

An electrochemical detection method for analyzing sequence-specific DNA using gold nanoparticle DNA probes and subsequent signal amplification step by silver enhancement is described. The assay relies on the electrostatic adsorption of starget oligonucleotides onto the sensing surface of the glass carbon electrode (GCE) and its hybridization to the gold nanoparticle-labeled oligonucleotides DNA probe. After silver deposition onto gold nanoparticles, binding events between probe and target were monitored by he differential pulse voltammetry (DPV) signal of the larger number of silver atoms anchored on the hybrids at the electrode surface. The signal intensity difference permits to distinguish between the match of two perfectly matched DNA strands and the near-perfect match where just one base pair was wrong. Coupled with this 'babioartucke-promoted' reduction of silver signal amplification method, the sensitivity of this electrochemical DNA biosensor has been increased by approximately two orders of magnitude and a detection limit of 50 pM of complementary oligonucleotides was obtained.
机译:描述了使用金纳米颗粒DNA探针分析序列特异性DNA的电化学检测方法,以及随后通过银增强的信号放大步骤。该测定法依赖于目标寡核苷酸在玻璃碳电极(GCE)感应表面上的静电吸附及其与金纳米颗粒标记的寡核苷酸DNA探针的杂交。在银沉积到金纳米颗粒上之后,通过差分脉冲伏安法(DPV)信号监测锚定在电极表面杂化物上的大量银原子,从而监测探针与靶之间的结合事件。信号强度的差异可以区分两条完全匹配的DNA链的匹配与仅一对碱基错误的近乎完美的匹配。结合这种“乳突促进的”还原银信号扩增方法,该电化学DNA生物传感器的灵敏度提高了大约两个数量级,并且获得了50 pM互补寡核苷酸的检测限。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号