首页> 外文会议>NSTI Nanotechnology Conference and Trade Show(NSTI Nanotech 2005) vol.1; 20050508-12; Anaheim,CA(US) >Electrical Detection of DNA Hybridization using Adjacent Impedance Probing (AIP) Method
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Electrical Detection of DNA Hybridization using Adjacent Impedance Probing (AIP) Method

机译:使用邻近阻抗探测(AIP)方法电检测DNA杂交

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Sensitivity and selectivity are two of the most challenging criteria for the development of DNA biosensor devices. These biosensor devices have attracted interest for the rapid identification of pathogens in humans, animals, and plants, for the detection of specific genes in animal and plant breeding and in the diagnosis of human genetic disorders. Traditionally, molecular diagnostic detection has relied on fluorescent or radioactive labels, and signal transduction is performed with equipment that greatly increases size and cost of the whole system. Electronic detection is expected to involve less complicated and smaller instrumentation while detection limits are maintained. Previous efforts on impedance-based DNA biosensors show limitations on repeatability, sensitivity and selectivity. In this work, we introduce the Adjacent Impedance Probing (AIP) technique for DNA hybridization detection. In this novel method, the DNA hybridization site is employed for the bio-recognition event (this site does not necessarily need an underlying conductor surface) and a bare adjacent conductor electrode is employed for generating the largest possible impedance change through the deposition of an insulating material or through chemical passivation induced by the enzymatic reporter reaction. The AIP approach dramatically increases the assay platform's perfomance vs. the previously employed technique that integrates the impedance electrode and the DNA capture probes. In the case of AIP, the impedance of the bare electrode is lower than that of a conductor surface modified with a self-assembled monolayer (SAM) of probe molecules and will not be subject to the irreproducibility associated with fabrication of such a SAM layer; as a consequence the S/N ratio will increase. The novel detection scheme demonstrated in this work is expected to find real applications for fields in diagnostics and biowarfare agent detection.
机译:灵敏度和选择性是DNA生物传感器设备开发中最具挑战性的两个标准。这些生物传感器设备引起了人们的兴趣,它们用于快速识别人类,动物和植物中的病原体,检测动植物育种中的特定基因以及诊断人类遗传疾病。传统上,分子诊断检测依赖于荧光或放射性标记,并且信号转导是使用大大增加整个系统的尺寸和成本的设备进行的。在保持检测极限的同时,电子检测有望减少复杂性和规模。以前基于阻抗的DNA生物传感器的研究显示出重复性,灵敏度和选择性方面的局限性。在这项工作中,我们介绍了用于DNA杂交检测的相邻阻抗探测(AIP)技术。在这种新方法中,将DNA杂交位点用于生物识别事件(该位点不一定需要下面的导体表面),并且使用裸露的相邻导体电极通过沉积绝缘层来产生最大可能的阻抗变化。物质或通过酶报告反应引起的化学钝化。与以前采用的将阻抗电极和DNA捕获探针整合在一起的技术相比,AIP方法大大提高了测定平台的性能。在AIP的情况下,裸电极的阻抗低于用探针分子的自组装单分子层(SAM)修饰的导体表面的阻抗,并且不会受到与制造此类SAM层相关的不可再现性的影响;结果,信噪比将增加。这项工作中展示的新颖检测方案有望在诊断和生物战剂检测领域找到实际应用。

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