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Gold-based optical biosensor for single-mismatched DNA detection using salt-induced hybridization

机译:基于金的光学生物传感器,用于利用盐诱导的杂交技术进行单错配DNA检测

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摘要

In this study, a gold nanoparticle (Au-NP)-based detection method for sensitive and specific DNA-based diagnostic applications is described. A sandwich format consisting of Au-NPs/DNA/PMP (Streptavidin-coated MagnetSphere Para-Magnetic Particles) was fabricated. PMPs captured and separated target DNA while Au-NPs modified with oligonucleotide detection sequences played a role in recognition and signal production. Due to the much lower stability of mismatched DNA strands caused by unstable duplex structures in solutions of relatively low salt concentration, hybridization efficiency in the presence of different buffers was well investigated, and thus, the optimized salt concentration allowed for discrimination of single-mismatched DNA (MMT) from perfectly matched DNA (PMT). Therefore, quantitative information concerning the target analyte was translated into a colorimetric signal, which could easily and quantitatively measured by low-cost UV-vis spectrophotometric analysis. The results indicated this to be a very simple and economic strategy for detection of single-mismatched DNA strands.
机译:在这项研究中,描述了一种基于金纳米粒子(Au-NP)的检测方法,用于敏感和特定的基于DNA的诊断应用。制作了由Au-NPs / DNA / PMP(链霉亲和素包被的MagnetSphere顺磁性粒子)组成的三明治格式。 PMP捕获并分离了目标DNA,而寡核苷酸检测序列修饰的Au-NP在识别和信号产生中发挥了作用。由于在较低盐浓度的溶液中由不稳定的双链体结构引起的错配DNA链的稳定性要低得多,因此在不同缓冲液存在下的杂交效率得到了很好的研究,因此,优化的盐浓度可以区分单错配的DNA (MMT)来自完美匹配的DNA(PMT)。因此,有关目标分析物的定量信息被转换为比色信号,可以通过低成本的紫外可见分光光度法轻松定量地测量。结果表明,这是检测单个错配DNA链的非常简单且经济的策略。

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