Enzymatic Assembly of DNA Nanostructures and Fragments with Sequence Overlaps

被引:3
|
作者
Chen, Rong [1 ]
Feng, Shuang [2 ]
Ren, Jieling [1 ]
Kang, Hong [1 ]
Yang, Yufan [1 ]
Xia, Ninuo [2 ,3 ]
Fang, Fang [3 ]
Wei, Bryan [1 ]
机构
[1] Tsinghua Univ, Peking Univ Ctr Life Sci, Ctr Synthet & Syst Biol, Sch Life Sci, Beijing 100084, Peoples R China
[2] CodeR Therapeut Ltd, Hefei 230000, Anhui, Peoples R China
[3] Univ Sci & Technol China, Affiliated Hosp USTC 1, Div Life Sci & Med, Hefei 230027, Anhui, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
HOMOLOGOUS RECOMBINATION; CLONING; DESIGN; SHAPES;
D O I
10.1021/jacs.3c01214
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Homologous recombination, an evolutionarily conserved DNA double-strand break repair pathway to protect genome stability, has long been exploited for the in vivo and in vitro assembly of multiple DNA duplex fragments in molecular cloning. Whether such methods can also be applied in the self-assembly of DNA nanostructures remains underexplored. Here, we report an enzymatic approach for the self-assembly of high-order DNA constructs with overlapping segments. In our system, a DNA polymerase with exonuclease activity was introduced to produce ssDNA overhangs for specific sticky end cohesion, and as many as 25 DNA structural units were designed to be hierarchically assembled. Using this approach, we successfully constructed a variety of high-order DNA nanostructures, including tubes and extended oligomers, from homogeneous assembly and custom multimers from heterogeneous assembly. Our strategy expands the construction toolbox of complex DNA nanostructures and highlights the potential to enhance the assembly of duplex fragments in molecular cloning.
引用
收藏
页码:9176 / 9181
页数:6
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