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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >A rapid method for detection of genetically modified organisms based on magnetic separation and surface-enhanced Raman scattering
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A rapid method for detection of genetically modified organisms based on magnetic separation and surface-enhanced Raman scattering

机译:基于磁分离和表面增强拉曼散射的快速检测转基因生物的方法

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摘要

In this study, a new method combining magnetic separation (MS) and surface-enhanced Raman scattering (SERS) was developed to detect genetically modified organisms (GMOs). An oligonucleotide probe which is specific for 35 S DNA target was immobilized onto gold coated magnetic nanospheres to form oligonucleotide-coated nanoparticles. A self assembled monolayer was formed on gold nanorods using 5,5′-dithiobis (2-nitrobenzoic acid) (DTNB) and the second probe of the 35 S DNA target was immobilized on the activated nanorod surfaces. Probes on the nanoparticles were hybridized with the target oligonucleotide. Optimization parameters for hybridization were investigated by high performance liquid chromatography. Optimum hybridization parameters were determined as: 4 μM probe concentration, 20 min immobilization time, 30 min hybridization time, 55 °C hybridization temperature, 750 mM buffer salt concentration and pH: 7.4. Quantification of the target concentration was performed via SERS spectra of DTNB on the nanorods. The correlation between the target concentration and the SERS signal was found to be linear within the range of 25-100 nM. The analyses were performed with only one hybridization step in 40 min. Real sample analysis was conducted using Bt-176 maize sample. The results showed that the developed MS-SERS assay is capable of detecting GMOs in a rapid and selective manner.
机译:在这项研究中,开发了一种结合磁分离(MS)和表面增强拉曼散射(SERS)的新方法来检测转基因生物(GMO)。将特异于35 S DNA靶标的寡核苷酸探针固定在金包被的磁性纳米球上,以形成寡核苷酸包被的纳米颗粒。使用5,5'-二硫代双(2-硝基苯甲酸)(DTNB)在金纳米棒上形成自组装单层,并将35 S DNA靶标的第二个探针固定在活化的纳米棒表面上。纳米颗粒上的探针与靶寡核苷酸杂交。通过高效液相色谱法研究了杂交的优化参数。最佳杂交参数确定为:4μM探针浓度,20分钟固定时间,30分钟杂交时间,55°C杂交温度,750 mM缓冲盐浓度和pH:7.4。通过DTNB在纳米棒上的SERS光谱对目标浓度进行定量。发现目标浓度和SERS信号之间的相关在25-100 nM范围内呈线性关系。在40分钟内仅进行一个杂交步骤即可进行分析。使用Bt-176玉米样品进行真实样品分析。结果表明,开发的MS-SERS检测方法能够快速,选择性地检测转基因生物。

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