Reconfigurable Two-Dimensional DNA Lattices: Static and Dynamic Angle Control

被引:18
|
作者
Wang, Wen [1 ]
Chen, Chunyu [1 ]
Vecchioni, Simon [2 ]
Zhang, Tianqing [1 ]
Wu, Chengxian [1 ]
Ohayon, Yoel P. [2 ]
Sha, Ruojie [2 ]
Seeman, Nadrian C. [2 ]
Wei, Bryan [1 ]
机构
[1] Tsinghua Univ, Tsinghua Univ Peking Univ Ctr Life Sci, Ctr Synthet & Syst Biol, Sch Life Sci, Beijing 100084, Peoples R China
[2] NYU, Dept Chem, 4 Washington Pl, New York, NY 10003 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
angle control; branching orientation; DNA nanostructures; junction motif; self-assembly; NUCLEIC-ACID JUNCTIONS; HOLLIDAY JUNCTION; FOLDING DNA; DESIGN; COMPLEXES; SEQUENCE; ARRAYS;
D O I
10.1002/anie.202112487
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Branched DNA motifs serve as the basic construction elements for all synthetic DNA nanostructures. However, precise control of branching orientation remains a key challenge to further heighten the overall structural order. In this study, we use two strategies to control the branching orientation. The first one is based on immobile Holliday junctions which employ specific nucleotide sequences at the branch points which dictate their orientation. The second strategy is to use angle-enforcing struts to fix the branching orientation with flexible spacers at the branch points. We have also demonstrated that the branching orientation control can be achieved dynamically, either by canonical Watson-Crick base pairing or non-canonical nucleobase interactions (e.g., i-motif and G-quadruplex). With precise angle control and feedback from the chemical environment, these results will enable novel DNA nanomechanical sensing devices, and precisely-ordered three-dimensional architectures.
引用
收藏
页码:25781 / 25786
页数:6
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