Parameters guiding the self-assembly of quantum dots and DNA origami by peptide-PNA

Christopher M. Green, D. Hastman, Divita Mathur, K. Susumu, Igor L. Medintz, S. A. Díaz
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Abstract

Nanoparticle (NP)-binding peptides conjugated to peptide nucleic acids - peptide-PNA - enable efficient and programmable self-assembly of quantum dots (QDs) on DNA nanostructures. As an alternative to chemically modified DNA, peptide-PNA were designed with a poly-histidine peptide motif (Histag) to enable self-assembly to the surface of ZnS-shelled QDs, along with a PNA domain which could undergo hybridization to a complementary DNA sequence by Watson-Crick base pairing. We have demonstrated that QDs can be conjugated efficiently to DNA origami by peptide-PNA without requiring a large excess of the individual components. Here, optimization was performed to assess the effects of varied molar ratios of peptide-PNA:QDs and QDs:origami on the binding efficiency of QDs to DNA origami.
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多肽- pna诱导量子点自组装和DNA折纸的参数
结合肽核酸的纳米粒子(NP)结合肽(peptide- pna)能够在DNA纳米结构上实现量子点(QDs)的高效可编程自组装。作为化学修饰DNA的替代方案,peptide-PNA设计了一个多组氨酸肽基序(Histag),使其能够自组装到zns壳量子点的表面,以及一个可以通过Watson-Crick碱基配对与互补DNA序列杂交的PNA结构域。我们已经证明量子点可以通过肽- pna有效地偶联到DNA折纸上,而不需要大量过量的单个组分。本研究通过优化来评估多肽- pna:QDs和QDs:origami的不同摩尔比对QDs与DNA origami结合效率的影响。
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