Fang Cheng, Fan Yi, Kong Jinming, Gao Zhiqiang, Balasubramanian Narayanan
Institute of Microelectronics, Agency for Science, Technology and Research, 11 Science Park Road, Science Park II, 117685, Republic of Singapore.
Anal Chem. 2008 Dec 15;80(24):9387-94. doi: 10.1021/ac801433z.
Sequence-specific DNA detection is a routine job in medical diagnostics and genetic screening. Alternative to a fluorescence readout scheme or electrophoresis approach, various kinds of rapid, low-cost, facile, and label-free methods have also been developed in last decades. Among these, direct electrical detection of DNA received increasing attention but more research is desirable. Particularly, enhancement with high discrimination must be employed to selectively amplify the responding signal. A chip-based biosensor was developed in this work to electrically detect 22-mer oligonucleotide DNA at low concentration, from 50 fM to 10 pM. First, a gold nanoparticle (NP) was capped with 3-mercaptopropionic acid through a thiol-gold bond. The derivatized carboxylic acid group showed strong complex interaction with an inorganic linker, Zr(4+). As a result, Zr(4+) could link several hundreds of individual gold NPs together to form an aggregate of nanoparticles (ANP), which was capable of being used as a conductive tag for the electrical detection of DNA. Second, in order to achieve the discriminative localization of ANP to bridge two comb-shaped electrodes (with height of approximately 50 nm and interdistance of 300-350 nm) gapped with insulative material of silicon oxide, peptide nucleic acids were covalently bonded to the silicon oxide in the gap as capture sites for DNA. After hybridization with target DNA, the charged phosphate-containing backbone of DNA was introduced into the gap. Phosphate groups also exhibited strong complex interaction with the linker of Zr(4+) and could react with the residual Zr(4+) on the ANP surface. As a consequence, the conductive tags were linked to the phosphate groups and localized into the gap, which could modify the conductance between the two comb-shaped electrodes in turn. The degree of modification correlated directly to the amount of hybridized DNA and to the concentration of target DNA in sample solution. Compared with the individual NPs used as the tag, a strong enhancement from the gold ANP was obtained.
序列特异性DNA检测是医学诊断和基因筛查中的一项常规工作。除了荧光读出方案或电泳方法外,在过去几十年中还开发了各种快速、低成本、简便且无标记的方法。其中,DNA的直接电学检测受到越来越多的关注,但仍需要更多的研究。特别是,必须采用具有高辨别力的增强方法来选择性地放大响应信号。在这项工作中,开发了一种基于芯片的生物传感器,用于电学检测低浓度(50 fM至10 pM)的22聚体寡核苷酸DNA。首先,通过硫醇-金键用3-巯基丙酸包覆金纳米颗粒(NP)。衍生化的羧酸基团与无机连接体Zr(4+)表现出强烈的络合相互作用。结果,Zr(4+)可以将数百个单个金纳米颗粒连接在一起形成纳米颗粒聚集体(ANP),其能够用作DNA电学检测的导电标签。其次,为了实现ANP在间隔有氧化硅绝缘材料的两个梳状电极(高度约为50 nm,间距为300-350 nm)之间的辨别性定位,将肽核酸共价键合到间隙中的氧化硅上作为DNA的捕获位点。与目标DNA杂交后,DNA含磷酸的带电荷主链被引入间隙。磷酸基团也与Zr(4+)的连接体表现出强烈的络合相互作用,并能与ANP表面残留的Zr(4+)反应。因此,导电标签与磷酸基团相连并定位到间隙中,这反过来又可以改变两个梳状电极之间的电导率。修饰程度与杂交DNA的量和样品溶液中目标DNA的浓度直接相关。与用作标签的单个纳米颗粒相比,金ANP获得了强烈的增强。