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Conjugation of DNA to Streptavidin-coated Quantum Dots for the Real-time Imaging of Gene Transfer into Live Cells

机译:DNA与链霉亲和素包被的量子点的缀合,用于实时成像转移到活细胞中的基因

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We have developed the method for the conjugation of biotinylated DNA to streptavidin-coated quantum dots (QDs). QD-DNA conjugates and a highly sensitive fluorescence imaging technique are adopted to visualize gene transport across the membrane of the live cell in real time. Endocytotic cellular uptake of oligonucleotide is monitored by a real-time confocal imaging system. Long-term kinetic study enables us to reveal the unknown mechanisms and rate-limiting steps of extracellular and intracellular transport of DNA. Gel electrophoresis is used to verify the effect of incubation time and the molar ratio of QDs to DNA on the conjugation efficiency. It is possible to fractionate the QD-DNA conjugates according to the DNA concentration and obtain the purified conjugates by a gel extraction technique. QD-DNA conjugates have a potential to be nanoscale building blocks by self-assembly process as well as a versatile tool for fluorescence imaging and monitoring of biological systems.
机译:我们已经开发了将生物素化的DNA与链霉亲和素包被的量子点(QD)结合的方法。 QD-DNA共轭物和高灵敏度的荧光成像技术被用来实时可视化跨活细胞膜的基因转运。寡核苷酸的胞吞细胞摄取通过实时共聚焦成像系统进行监控。长期的动力学研究使我们能够揭示DNA细胞外和细胞内运输的未知机制和限速步骤。凝胶电泳用于验证孵育时间和QD与DNA的摩尔比对缀合效率的影响。可以根据DNA浓度对QD-DNA结合物进行分级分离,并通过凝胶提取技术获得纯化的结合物。 QD-DNA共轭物具有通过自组装过程成为纳米级构建基块的潜力,以及用于荧光成像和生物系统监控的多功能工具。

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