Nanomaterials and Chemistry Key Laboratory, College of Chemistry and Chemical Engineering, Wenzhou University , Wenzhou, Zhejiang 325027, People's Republic of China.
Anal Chem. 2014 Jan 21;86(2):1178-85. doi: 10.1021/ac4032675. Epub 2013 Dec 30.
A simple and sensitive gap-electrical biosensor based on self-catalytic growth of unmodified gold nanoparticles (AuNPs) as conductive bridges has been developed for amplifying DNA hybridization events. In this strategy, the signal amplification degree of such conductive bridges is closely related to the variation of the glucose oxidase (GOx)-like catalytic activity of AuNPs upon interaction with single- and double-stranded DNA (ssDNA and dsDNA), respectively. In the presence of target DNA, the obtained dsDNA product cannot adsorb onto the surface of AuNPs due to electrostatic interaction, which makes the unmodified AuNPs exhibit excellent GOx-like catalytic activity. Such catalytic activity can enlarge the diameters of AuNPs in the glucose and HAuCl4 solution and result in a connection between most of the AuNPs and a conductive gold film formation with a dramatically increased conductance. For the control sample, the catalytic activity sites of AuNPs are fully blocked by ssDNA due to the noncovalent interaction between nucleotide bases and AuNPs. Thus, the growth of the assembled AuNPs will not happen and the conductance between microelectrodes will be not changed. Under the optimal experimental conditions, the developed strategy exhibited a sensitive response to target DNA with a high signal-to-noise ratio. Moreover, this strategy was also demonstrated to provide excellent differentiation ability for single-nucleotide polymorphism. Such performances indicated the great potential of this label-free electrical strategy for clinical diagnostics and genetic analysis under real biological sample separation.
一种基于未经修饰的金纳米粒子(AuNPs)自催化生长作为导电桥的简单灵敏的间隙电生物传感器已被开发用于放大 DNA 杂交事件。在该策略中,这种导电桥的信号放大程度与 AuNPs 与单链和双链 DNA(ssDNA 和 dsDNA)相互作用时的葡萄糖氧化酶(GOx)样催化活性的变化密切相关。在存在靶 DNA 的情况下,由于静电相互作用,所得的 dsDNA 产物不能吸附到 AuNPs 表面上,这使得未经修饰的 AuNPs 表现出优异的 GOx 样催化活性。这种催化活性可以在葡萄糖和 HAuCl4 溶液中扩大 AuNPs 的直径,并导致大多数 AuNPs 与导电金膜形成连接,从而导致电导显著增加。对于对照样品,由于核苷酸碱基与 AuNPs 之间的非共价相互作用,AuNPs 的催化活性位点被 ssDNA 完全阻断。因此,组装的 AuNPs 的生长不会发生,并且微电极之间的电导将不会改变。在最佳实验条件下,所开发的策略对目标 DNA 表现出高信噪比的灵敏响应。此外,该策略还被证明为单核苷酸多态性提供了出色的区分能力。这些性能表明,这种无标记的电策略在实际生物样品分离下的临床诊断和遗传分析中具有巨大的潜力。