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利用金纳米粒子修饰电极电化学检测植物病毒。

Electrochemical detection of plant virus using gold nanoparticle-modified electrodes.

机构信息

Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and Barcelona Institute of Science and Technology, Campus UAB, 08193, Barcelona, Spain; On Leave from Agricultural Research Center (ARC), Ministry of Agriculture and Land Reclamation, Giza, Egypt.

Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and Barcelona Institute of Science and Technology, Campus UAB, 08193, Barcelona, Spain.

出版信息

Anal Chim Acta. 2019 Jan 10;1046:123-131. doi: 10.1016/j.aca.2018.09.031. Epub 2018 Sep 15.

Abstract

Tristeza is one of the destructive diseases of citrus causing by citrus tristeza virus (CTV). Historically, CTV has been associated with serious outbreaks of quick decline of citrus, therefore CTV monitoring is important aspect for avoiding such re-emerging epidemics, which would threat citrus production through the world. In this context, we have designed for the first time a label-free impedimetric biosensor for the detection of nucleic acid of CTV. The sensing platform based on a screen-printed carbon electrode (SPCE) was modified by electrodeposited gold nanoparticles (AuNPs), which allowed to efficiently immobilizing thiolated ssDNA probes as well to enhance the electrode conductivity. The growth of AuNPs was optimized and characterized using scanning electron microscopy (SEM), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). We investigated the behavior of thiolated ssDNA probe layer and its hybridization with target DNA onto AuNP surfaces by EIS measurements in Fe(CN)/Fe(CN) red-ox system. The main sensor design aspects such as AuNPs size, probe DNA concentration and immobilization time together with DNA hybridization time were optimized so as to achieve the best performance. Impedance values of DNA hybridization increased with Citrus tristeza-related synthetic DNA concentration, showing a logarithmic relation in the range of 0.1-10 μM. The results also indicate that the biosensor was able to selectively detect CTV nucleic acids in the presence of other non-specific DNAs. Moreover, we have demonstrated the good performance of the system in a real plant sample matrix. In addition, the sensor reproducibility enhanced after the hybridization onto MCH/poly (AT) thiolated DNA probes which was confirmed by intra- and inter-day variability assays.

摘要

悲伤是柑橘毁灭性疾病之一,由柑橘衰退病毒(CTV)引起。从历史上看,CTV 与柑橘快速衰退的严重疫情有关,因此,CTV 监测是避免此类疫情再次出现的重要方面,这将威胁到全球的柑橘生产。在这种情况下,我们首次设计了一种用于检测 CTV 核酸的无标记阻抗生物传感器。基于丝网印刷碳电极(SPCE)的传感平台通过电沉积金纳米粒子(AuNPs)进行了修饰,这使得能够有效地固定巯基化 ssDNA 探针,并增强电极的导电性。使用扫描电子显微镜(SEM)、循环伏安法(CV)和电化学阻抗谱(EIS)对 AuNPs 的生长进行了优化和表征。我们通过在 Fe(CN)/Fe(CN)氧化还原体系中进行 EIS 测量,研究了 AuNP 表面上巯基化 ssDNA 探针层及其与目标 DNA 的杂交行为。优化了传感器设计的主要方面,如 AuNPs 尺寸、探针 DNA 浓度和固定化时间以及 DNA 杂交时间,以达到最佳性能。DNA 杂交的阻抗值随与柑橘悲伤相关的合成 DNA 浓度的增加而增加,在 0.1-10 μM 的范围内呈对数关系。结果还表明,该生物传感器能够在存在其他非特异性 DNA 的情况下选择性地检测 CTV 核酸。此外,我们已经证明了该系统在真实植物样本基质中的良好性能。此外,通过在 MCH/poly(AT)巯基化 DNA 探针上进行杂交,提高了传感器的重现性,这通过日内和日间变异性测定得到了证实。

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