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Bioactivation of water-soluble peptidic quantum dot through biotin-streptavidin binding

机译:通过生物素 - 链霉抗生物素蛋白结合的水溶性肽量子点的生物活化

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This paper describes the preparation of bioactive water-soluble fluorescent CdSe/ZnS semi-conductor quantum dots with a small hydrodynamic diameter of 10 nm. These quantum dots are functionalized with a biotinylated peptide that can be introduced at different ratios onto the surface of the quantum dots. Their ability to bind to streptavidin in solution is tested by using gel electrophoresis and fluorescence resonance energy transfer with a fluorescent labeled-streptavidin. The binding of these quantum dots to Agarose micrometric beads coated with streptavidin is also analyzed by fluorescent optical microscopy. A synthetic pegylated peptide is successfully used to prevent the non specific adsorption of streptavidin onto the quantum dots. A specific binding to the streptavidin results in the formation of a very stable streptavidin-quantum dot complex without any significant aggregation. The average number of streptavidin per quantum dot is found to be to 4 at the most. Such bioactivate quantum dots can be further conjugated to any biotinylated biomolecule and used in biological medium.
机译:本文描述了具有10nm的小流体动力直径的生物活性水溶性荧光CdSe / ZnS半导体量子点的制备。这些量子点用生物素化的肽官能化,其可以以不同的比例引入量子点的表面上。通过使用凝胶电泳和荧光共振能量与荧光标记的链霉抗生物素蛋白来测试它们在溶液中与链霉抗生物素蛋白结合的能力。还通过荧光光学显微镜分析这些量子点与涂有链霉抗生物素蛋白的琼脂糖微米珠的结合。合成的聚乙二醇化肽已成功地用于防止在量子点上的表霉抗生物素蛋白的非比吸附。与链霉抗生物素蛋白的特异性结合导致形成非常稳定的链霉抗生物素蛋白 - 量子点复合物,而没有任何显着的聚集。发现每个量子点的平均链霉蛋白的数量最多。这种生物贴活量子点可以进一步与任何生物素化的生物分子缀合并用于生物培养基中。

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