Department of Chemistry, Zhejiang University, Hangzhou 310058, China.
Department of Chemistry, Zhejiang University, Hangzhou 310058, China.
Biosens Bioelectron. 2019 Feb 15;127:101-107. doi: 10.1016/j.bios.2018.12.019. Epub 2018 Dec 15.
Despite rapid progress in DNA biosensors by employing various materials as well as techniques, most of the reported sensors are based on specific recognition of a DNA fragment, however can not perform universal measurement of DNA molecules (i.e. genomic DNA). In this work, we proposed a novel DNA biosensing method based on instantaneously electrostatic attraction (IEA) between hexaammineruthenium (III) and DNA molecules. The current variation of freely diffused Ru(NH) caused by its quick and strong static interaction with phosphate backbones was employed as a universal probe to detect DNA molecules in solution, with no need for immobilization of capture probes on the electrode. After optimization, 30 μL of 300 μM Ru(NH) solution was added onto the gold electrode with a working electrode diameter of 2 mm, and a detection limit of 3.8 ng/μL was achieved, which is equivalent to NanoDrop™ One spectrometer, the commonly used instrument for DNA quantification. Using reusable and inexpensive gold electrode, the approach provided an easy-operated sequence-independent DNA detection method, and was proved to be able to detect genomic and plasmid DNA directly.
尽管采用各种材料和技术在 DNA 生物传感器方面取得了快速进展,但大多数报道的传感器都是基于对特定 DNA 片段的特异性识别,然而无法对 DNA 分子(即基因组 DNA)进行通用测量。在这项工作中,我们提出了一种基于六氨合钌 (III) 与 DNA 分子之间瞬间静电吸引 (IEA) 的新型 DNA 生物传感方法。通过快速且强烈的静电相互作用与磷酸骨架结合,自由扩散的 Ru(NH) 的电流变化被用作溶液中 DNA 分子的通用探针,无需将捕获探针固定在电极上。经过优化,在工作电极直径为 2mm 的金电极上加入 30μL 浓度为 300μM 的 Ru(NH)溶液,检测限达到 3.8ng/μL,与常用于 DNA 定量的 NanoDrop™ One 分光光度计相当。使用可重复使用且廉价的金电极,该方法提供了一种易于操作、无需序列依赖的 DNA 检测方法,并被证明能够直接检测基因组和质粒 DNA。