Dynamic Tuning of DNA-Nanoparticle Superlattices by Molecular Intercalation of Double Helix

被引:53
作者
Pal, Suchetan [1 ,2 ]
Zhang, Yugang [2 ]
Kumar, Sanat K. [1 ]
Gang, Oleg [2 ]
机构
[1] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
关键词
BINDING;
D O I
10.1021/ja512799d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoparticle (NP) assembly using DNA recognition has emerged as a powerful tool for the fabrication of 3D superlattices. In addition to the vast structural diversity, this approach provides an avenue for dynamic 3D NP assembly, which is promising for the modulation of interparticle distances and, hence, for example, for in situ tuning of optical properties. While several approaches have been explored for changing NP separations in the lattices using responsiveness of single-stranded DNA (ss-DNA), far less work has been done for the manipulation of most abundant double-stranded DNA (ds-DNA) motifs. Here, we present a novel strategy for modulation of interparticle distances in DNA linked 3D self-assembled NP lattices by molecular intercalator. We utilize ethidium bromide (EtBr) as a model intercalator to demonstrate selective and isotropic lattice expansion for three superlattice types (bcc, fcc, and AlB2) due to the intercalation of ds-DNA linking NPs. We further show the reversibility of the lattice parameter using n-butanol as a retrieving agent as well as an increased lattice thermal stability by 12-14 degrees C due to the inclusion of EtBr. The proposed intercalator-based strategy permits the creation of reconfigurable and thermally stable superlattices, which could lead to tunable and functionally responsive materials.
引用
收藏
页码:4030 / 4033
页数:4
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