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Templated self-assembly of quantum dots from aqueous solution using protein scaffold

机译:使用蛋白质支架从水溶液中量子点的模板化自组装

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摘要

Short, histidine-containing peptides can be conjugated to lysine-containing protein scaffolds to controllabiy attach quantum dots (QDs) to the scaffold, allowing for generic attachment of quantum dots to any protein without the ire of specially engineered domains. This technique was used to bind quantum dots from aqueous solution to both chicken IgG and cowpea mosaic MILLS (CPMV), a 30 nm viral particle. These quantum dot-protein assemblies nere studied in detail. The IgG-QD complexes were shown to retain binding specificity to their antigen after modification. The CPMV-QD complexes luive a local concentration of quantum dots greater than 3000 nmol ml~(-1), and show a 15 percent increase in fluorescence quantum yield over free quantum dots in solution.
机译:可以将短的含组氨酸的肽与含赖氨酸的蛋白质支架偶联,以可控制地将量子点(QD)连接到支架上,从而允许将量子点通用地连接到任何蛋白质上而无需专门设计的结构域。该技术用于将水溶液中的量子点与鸡IgG和cow豆花叶MILLS(CPMV)(一种30 nm病毒颗粒)结合。这些量子点蛋白组装需要详细研究。修饰后,IgG-QD复合物显示出对抗原的结合特异性。 CPMV-QD络合物的量子点局部浓度大于3000 nmol ml-1(-1),并且荧光量子产率比溶液中的自由量子点提高了15%。

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