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基于双重超级聚合酶链反应和侧向流生物传感器的双基因修饰元件的超快、通用和可视化筛选。

Ultrafast, universal and visual screening of dual genetically modified elements based on dual super PCR and a lateral flow biosensor.

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Food Science & Nutritional Engineering, China Agricultural University, Beijing 100083, China.

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Food Science & Nutritional Engineering, China Agricultural University, Beijing 100083, China; Key Laboratory of Safety Assessment of Genetically Modified Organism (Food Safety), Ministry of Agriculture, Beijing 100083, China.

出版信息

Food Chem. 2019 May 1;279:246-251. doi: 10.1016/j.foodchem.2018.12.013. Epub 2018 Dec 10.

Abstract

In this study, a cascade screening system has been developed combining Dual Super Polymerase Chain Reaction (DSPCR) with the universal Lateral Flow Biosensor (LFB) for the ultrafast, universal and visual screening of dual GM elements, taking P-35s × T-nos for example. In the design of DSPCR for universal screening, gene-specific forward primers were labelled with biotin and gene-specific reverse primers were tagged with Cy5 and digoxin, respectively. In 2.5-min, DSPCR effectively amplified the dual target fragments through our prototype facility. Then, through specific antigen-antibody binding, a universal lateral flow biosensor exported visually dual-amplified results simultaneously without cross contamination. After optimization, the detection limit allowed 0.05% GM maize, corresponding to nine copies in maize. The entire detection process could be achieved in 10 min without any large-scale instrumentation. This method may be useful for the ultrafast, universal and visual screening of dual GM elements (P-35s × T-nos) in GM crop lines and is expected to be of great promise for rapid GMO screening and point-of-care tests.

摘要

在这项研究中,我们开发了一种级联筛选系统,将双重超级聚合酶链反应(DSPCR)与通用横向流动生物传感器(LFB)相结合,用于快速、通用和可视化筛选双 GM 元件,以 P-35s×T-nos 为例。在用于通用筛选的 DSPCR 设计中,基因特异性正向引物用生物素标记,基因特异性反向引物分别用 Cy5 和地高辛标记。在 2.5 分钟内,DSPCR 通过我们的原型设备有效地扩增了双靶片段。然后,通过特定的抗原-抗体结合,通用的横向流动生物传感器同时输出可视化的双扩增结果,而不会发生交叉污染。经过优化,检测限允许 0.05%的 GM 玉米,相当于玉米中的九个拷贝。整个检测过程可以在 10 分钟内完成,无需任何大型仪器。该方法可用于 GM 作物品系中双 GM 元件(P-35s×T-nos)的快速、通用和可视化筛选,有望在快速 GMO 筛选和即时检测方面具有广阔的应用前景。

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