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Surface Plasmon Resonance Detection of Transgenic Cry1Ac Cotton (Gossypium spp.)

机译:转基因Cry1Ac棉的表面等离子体共振检测

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The detection and identification of genetically modified (GM) plants are challenging issues that have arisen from the potential negative impacts of extensive cultivation of transgenic plants. The screening process is a long-term focus and needs specific detection strategies. Surface plasmon resonance (SPR) has been used to detect a variety of biomolecules including proteins and nucleic acids due to its ability to monitor specific intermolecular interactions. In the present study, two high-throughput, label-free, and specific methods based on SPR technology were developed to detect transgenic Cry1Ac cotton (Gossypium spp.) by separately targeting protein and DNA. In the protein-based detection system, monoclonal anti-Cry1Ac antibodies were immobilized on the surface of a CM5 sensor chip. Conventional cotton samples were used to define the detection threshold. Transgenic cotton was easily identified within 5 min per sample. For the DNA-based model, a 25-mer biotinylated oligonucleotide probe was immobilized on an SA sensor chip. PCR products of Cry1Ac (230 bp) were used to investigate the reaction conditions. The sensitivity of the constructed sensor chip was identified at concentrations as low as 0.1 nM based on its complementary base pairing.
机译:转基因植物的检测和鉴定是具有挑战性的问题,这些问题源于广泛种植转基因植物的潜在负面影响。筛选过程是长期的重点,需要特定的检测策略。由于其监测特定分子间相互作用的能力,表面等离振子共振(SPR)已被用于检测包括蛋白质和核酸在内的多种生物分子。在本研究中,开发了两种基于SPR技术的高通量,无标记和特定方法,通过分别靶向蛋白质和DNA来检测转基因Cry1Ac棉(棉)。在基于蛋白质的检测系统中,单克隆抗Cry1Ac抗体被固定在CM5传感器芯片的表面上。使用常规棉样品定义检测阈值。每个样品在5分钟内即可轻松鉴定出转基因棉花。对于基于DNA的模型,将25-mer生物素化的寡核苷酸探针固定在SA传感器芯片上。 Cry1Ac(230 bp)的PCR产物用于研究反应条件。基于其互补碱基配对,可在低至0.1 nM的浓度下识别出所构建传感器芯片的灵敏度。

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