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Distance-Dependent Metal-Enhanced Quantum Dots Fluorescence Analysis in Solution by Capillary Electrophoresis and Its Application to DNA Detection

机译:毛细管电泳法分析距离相关的金属增强量子点荧光及其在DNA检测中的应用

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Here the distance dependence of metal-enhanced quantum dots (QDs) fluorescence in solution is studied systematically by capillary electrophoresis (CE). Complementary DNA oligonucleotides-modified CdSe/ZnS QDs and gold nanoparticles (Au NPs) were connected together in solution by the hybridization of complementary oligonucleotides, and a model system (QD-Au) for the study of metal-enhanced QDs fluorescence was constructed, in which the distance between the QDs and Au NPs was controlled by adjusting the base number of the oligonucleotide. In our CE experiments, the metal-enhanced fluorescence of the QDs solution was only observed when the distance between the QDs and Au NPs ranged from 6.8 to 18.7 nm, and the maximum enhancement by a factor of 2.3 was achieved at 11.9 nm. Furthermore, a minimum of 19.6 pg of target DNA was identified in CE based on its specific competition with the QD-DNA in the QD-Au system. This work provides an important reference for future study of metal-enhanced QDs fluorescence in solution and exhibits potential capability in nucleic acid hybridization analysis and high-sensitivity DNA detection.
机译:在这里,通过毛细管电泳(CE)系统地研究了溶液中金属增强量子点(QDs)荧光的距离依赖性。通过互补寡核苷酸的杂交将互补的DNA寡核苷酸修饰的CdSe / ZnS量子点和金纳米颗粒(Au NPs)在溶液中连接在一起,并构建了用于研究金属增强QDs荧光的模型系统(QD-Au)。通过调节寡核苷酸的碱基数来控制QD和Au NP之间的距离。在我们的CE实验中,仅当QD和Au NP之间的距离在6.8至18.7 nm范围内时才观察到QDs溶液的金属增强荧光,并且在11.9 nm处获得最大2.3倍的增强。此外,根据CE与QD-Au系统中与QD-DNA的特异性竞争,在CE中鉴定出至少19.6 pg的目标DNA。这项工作为今后研究溶液中金属增强的QDs荧光提供了重要的参考,并在核酸杂交分析和高灵敏度DNA检测方面具有潜在的能力。

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