首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A one-step electrochemical method for DNA detection that utilizes a peroxidase-mimicking DNAzyme amplified through PCR of target DNA
【24h】

A one-step electrochemical method for DNA detection that utilizes a peroxidase-mimicking DNAzyme amplified through PCR of target DNA

机译:一步电化学检测DNA的方法,利用过氧化物酶模拟DNA酶通过目标DNA的PCR扩增

获取原文
获取原文并翻译 | 示例
           

摘要

A novel one-step electrochemical method for DNA detection is described. The procedure utilizes a reaction catalyzed by a peroxidase-mimicking DNAzyme to produce a product, which forms an insoluble precipitation layer on the surface of an electrode. A rationally designed forward primer, conjugated with a peroxidase DNAzyme complementary sequence at its 5'-end, is used for PCR amplification of target DNA. As a result, the DNAzyme sequence is produced by amplification only when the target DNA is present in the sample. The PCR product is then subjected to the precipitation reaction on the electrode surface using an electrolyte assay buffer containing 4-chloronaphthol, hydrogen peroxide, ferrocenemethanol, hemin, and 5'-lambdaexonuclease. Finally, analysis is carried out using Faradaic impedance spectroscopy. The impedance value was found to greatly increase when target DNA is present owing to the formation of a precipitation layer on the electrode surface caused by the catalytic action of the DNAzyme. In contrast, no impedance increase is observed when a control sample not containing target DNA is utilized. By employing this strategy, target DNA from Chlamydia trachomatis was reliably detected within a 10. min period following precipitation without the need for complicated secondary procedures. This effort has led to the development of a highly convenient electrochemical one-step method for DNA detection that utilizes a peroxidase-mimicking DNAzyme, which is specifically designed to undergo amplification during PCR of target DNA.
机译:描述了一种用于DNA检测的新颖的一步电化学方法。该方法利用过氧化物酶模拟DNAzyme催化的反应产生产物,该产物在电极表面形成不溶性沉淀层。合理设计的正向引物,在其5'末端与过氧化物酶DNAzyme互补序列偶联,可用于PCR扩增靶DNA。结果,仅当目标DNA存在于样品中时才通过扩增产生DNA核酶序列。然后使用含有4-氯萘酚,过氧化氢,二茂铁甲醇,血红素和5'-λ核酸外切酶的电解质分析缓冲液,使PCR产物在电极表面上进行沉淀反应。最后,使用法拉第阻抗谱进行分析。发现存在靶DNA时,由于DNA酶的催化作用在电极表面形成沉淀层,因此阻抗值大大增加。相反,当使用不含靶DNA的对照样品时,没有观察到阻抗增加。通过采用该策略,在沉淀后的10分钟内即可可靠地检测到沙眼衣原体的目标DNA,而无需进行复杂的第二步操作。这项工作已导致开发了一种非常方便的电化学一步检测DNA的方法,该方法利用了模仿过氧化物酶的DNAzyme,该酶是专门设计用于在目标DNA PCR期间进行扩增的。

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