Laser Processing and Plasmonics Laboratory, École Polytechnique de Montréal, Department of Engineering Physics, C.P. 6079, succ. Centre-Ville, Montréal, QC, Canada H3C 3A7.
Laboratory of Biosensors and Nanomachines, Université de Montréal, Department of Chemistry, C.P. 6128, succ. Centre-Ville, Montréal, QC, Canada H3C 3J7.
Biosens Bioelectron. 2015 Sep 15;71:75-81. doi: 10.1016/j.bios.2015.04.011. Epub 2015 Apr 7.
In this paper, we present the development of a nanoswitch-based electrochemical surface plasmon resonance (eSPR) transducer for the multiplexed and selective detection of DNA and other biomolecules directly in complex media. To do so, we designed an experimental set-up for the synchronized measurements of electrochemical and electro-plasmonic responses to the activation of multiple electrochemically labeled structure-switching biosensors. As a proof of principle, we adapted this strategy for the detection of DNA sequences that are diagnostic of two pathogens (drug-resistant tuberculosis and Escherichia coli) by using methylene blue-labeled structure-switching DNA stem-loop. The experimental sensitivity of the switch-based eSPR sensor is estimated at 5 nM and target detection is achieved within minutes. Each sensor is reusable several times with a simple 8M urea washing procedure. We then demonstrated the selectivity and multiplexed ability of these switch-based eSPR by simultaneously detecting two different DNA sequences. We discuss the advantages of the proposed eSPR approach for the development of highly selective sensor devices for the rapid and reliable detection of multiple molecular markers in complex samples.
在本文中,我们提出了一种基于纳米开关的电化学表面等离子体共振(eSPR)传感器的开发,用于直接在复杂介质中对 DNA 和其他生物分子进行多重和选择性检测。为此,我们设计了一种实验装置,用于同步测量电化学和电等离子体响应,以激活多个电化学标记的结构切换生物传感器。作为原理验证,我们通过使用亚甲蓝标记的结构切换 DNA 发夹,将这种策略适应于检测两种病原体(耐多药结核分枝杆菌和大肠杆菌)的诊断 DNA 序列。基于开关的 eSPR 传感器的实验灵敏度估计为 5 nM,并且可以在数分钟内实现目标检测。每次传感器都可以通过简单的 8M 尿素洗涤程序重复使用几次。然后,我们通过同时检测两种不同的 DNA 序列,证明了这些基于开关的 eSPR 的选择性和多重检测能力。我们讨论了所提出的 eSPR 方法在开发用于快速可靠检测复杂样品中多个分子标记的高度选择性传感器装置方面的优势。