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基于金碳点的无标记电化学阻抗 DNA 生物传感器用于转基因大豆检测。

A label-free electrochemical impedimetric DNA biosensor for genetically modified soybean detection based on gold carbon dots.

机构信息

Key Laboratory of Oil Crop Biology of the Ministry of Agriculture and Rural Affairs, Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan, 430062, China.

出版信息

Mikrochim Acta. 2022 May 10;189(6):216. doi: 10.1007/s00604-022-05223-7.

DOI:10.1007/s00604-022-05223-7
PMID:35536374
Abstract

A label-free electrochemical impedimetric biosensor was constructed based on gold carbon dots (GCDs) modified screen-printed carbon electrode for the detection of genetic modified (GM) soybean. The structure and property of GCDs were investigated. The GCDs can directly bind to single-stranded DNA probes through Au-thiol interaction and boost electric conductivity for the DNA sensor construction. The quantification of target DNA was monitored by the change of electron-transfer resistance (R) upon the DNA hybridization on sensor surface. Under the optimal conditions, the R response (vs. Ag reference electrode) increased with the logarithm of target DNA concentrations in a wide linear range of 1.0 × 10 - 1.0 × 10 M with a detection limit of 3.1 × 10 M (S/N = 3). It was also demonstrated that the proposed DNA sensor possessed high specificity for discriminating target DNA from mismatched sequences. Moreover, the developed biosensor was applied to detect SHZD32-1 in actual samples, and the results showed a good consistency with those obtained from the gel electrophoresis method. Compared with the previous reports for DNA detection, the label-free biosensor showed a comparatively simple platform due to elimination of complicated DNA labeling. Therefore, the proposed method showed great potential to be an alternative device for simple, sensitive, specific, and portable DNA sensor.

摘要

一种基于金碳点 (GCDs) 修饰的丝网印刷碳电极的无标记电化学阻抗生物传感器被构建用于检测转基因大豆。研究了 GCDs 的结构和性质。GCDs 可以通过 Au-硫醇相互作用直接与单链 DNA 探针结合,并增强 DNA 传感器构建的导电性。通过传感器表面 DNA 杂交后电子转移电阻 (R) 的变化来监测目标 DNA 的定量。在最佳条件下,R 响应(相对于 Ag 参比电极)随目标 DNA 浓度的对数在 1.0×10-1.0×10 M 的宽线性范围内增加,检测限为 3.1×10 M(S/N=3)。还证明了所提出的 DNA 传感器具有从错配序列中区分目标 DNA 的高特异性。此外,所开发的生物传感器被应用于实际样品中 SHZD32-1 的检测,结果与凝胶电泳法得到的结果具有良好的一致性。与以前用于 DNA 检测的报告相比,由于消除了复杂的 DNA 标记,无标记生物传感器显示出一个相对简单的平台。因此,该方法显示出作为一种简单、灵敏、特异、便携的 DNA 传感器的替代设备的巨大潜力。

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