DNA-Based Assembly of Quantum Dots into Dimers and Helices

被引:16
作者
Zhang, Tao [1 ,3 ]
Liedl, Tim [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen LMU, Fac Phys, D-80539 Munich, Germany
[2] Ludwig Maximilians Univ Munchen LMU, Ctr Nanosci CeNS, D-80539 Munich, Germany
[3] Max Planck Inst Intelligent Syst, D-70569 Stuttgart, Germany
关键词
quantum dots; DNA-QDs conjugation; DNA nanotechnology; ORIGAMI; NANOCRYSTALS; EMISSION; SHAPE; CDSE; CYTOTOXICITY; FABRICATION; ARRAYS;
D O I
10.3390/nano9030339
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Owing to their unique optical properties, colloidal quantum dots (QDs) have attracted much attention as versatile fluorescent markers with broad biological and physical applications. On the other hand, DNA-based assembly has proven to be a powerful bottom-up approach to create designer nanoscale objects and to use these objects for the site-directed arrangement of guest components. To achieve good colloidal stability and accurate positioning of QDs on DNA templates, robust QD surface functionalization is crucial. Here, we present a simple and reliable conjugation method for the direct attachment of DNA molecules to QDs. Phosphorothiolated regions of chimera oligonucleotides are attached and incorporated into a ZnS layer freshly growing in situ on QDs that were rendered water soluble with hydrophilic ligands in a prior step. The reaction can be completed in a 2 mL plastic tube without any special equipment. The utility of these DNA-labeled QDs is demonstrated via prototypical assemblies such as QDs dimers with various spacings and chiral helical architectures.
引用
收藏
页数:10
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