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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 >Sub-femtomolar DNA detection based on layered molybdenum disulfide/multi-walled carbon nanotube composites, Au nanoparticle and enzyme multiple signal amplification
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Sub-femtomolar DNA detection based on layered molybdenum disulfide/multi-walled carbon nanotube composites, Au nanoparticle and enzyme multiple signal amplification

机译:基于层状二硫化钼/多壁碳纳米管复合材料,金纳米粒子和酶多信号放大的亚飞摩尔DNA检测

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摘要

A novel 2-dimensional graphene analog molybdenum disulfide/multi-walled carbon nanotube (MoS2/ MWCNT) was synthesized by a simple hydrothermal method to achieve excellent electrochemical properties. An ultrasensitive electrochemical DNA biosensor was subsequently constructed by assembling a thiol-tagged DNA probe on a MoS2/MWCNT and gold nanoparticle (AuNP)-modified electrode that has already been coupled with glucose oxidase (GOD). In this work, GOD was used as a redox marker. The heteronanostructure formed on the biosensor surface appeared relatively good conductor for accelerating the electron transfer, while the modification of GOD and AuNPs provided multiple signal amplification for electrochemical biosensing. The multiple signal amplification strategy produced an ultrasensitive electrochemical detection of DNA down to 0.79 fM with a linear range from 10 fM to 10~7 fM, and appeared high selectivity to differentiate three-base mismatched DNA and one-base mismatched DNA. The developed approach provided a simple and reliable method for DNA detection with high sensitivity and specificity, and would open new opportunities for sensitive detection of other biorecognition events.
机译:通过简单的水热法合成了新型的二维石墨烯类似物二硫化钼/多壁碳纳米管(MoS2 / MWCNT),获得了优异的电化学性能。随后,通过在MoS2 / MWCNT和已经与葡萄糖氧化酶(GOD)偶联的金纳米颗粒(AuNP)修饰的电极上组装硫醇标记的DNA探针,构建了超灵敏的电化学DNA生物传感器。在这项工作中,GOD被用作氧化还原标记。生物传感器表面上形成的异质结构似乎是用于加速电子转移的相对较好的导体,而修饰的GOD和AuNPs为电化学生物传感提供了多种信号放大。多重信号放大策略可对DNA进行超灵敏的电化学检测,检测范围从10 fM到10〜7 fM的线性低至0.79 fM,并且对区分三碱基错配DNA和一碱基错配DNA表现出很高的选择性。所开发的方法为DNA检测提供了一种简单而可靠的方法,具有很高的灵敏度和特异性,并为其他生物识别事件的敏感检测提供了新的机会。

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