A Facile Method for Preparation of Tailored Scaffolds for DNA-Origami

被引:39
作者
Erkelenz, Michael [1 ]
Bauer, Dennis M. [1 ,2 ]
Meyer, Rebecca [1 ,5 ]
Gatsogiannis, Christos [3 ]
Raunser, Stefan [3 ]
Sacca, Barbara [1 ,4 ]
Niemeyer, Christof M. [1 ,5 ]
机构
[1] Tech Univ Dortmund, Fak Chem, D-44227 Dortmund, Germany
[2] Karlsruhe Inst Technol KIT, DFG Ctr Funct Nanostruct CFN, D-76131 Karlsruhe, Germany
[3] Max Planck Inst Mol Physiol, D-44227 Dortmund, Germany
[4] Univ Duisburg Essen, Zentrum Med Biotechnol ZMB, Fak Biol, D-45117 Essen, Germany
[5] Karlsruhe Inst Technol KIT, Inst Biol Interfaces IBG 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
bacterial cloning; DNA; nanostructures; self-assembly; FOLDING DNA; NANOSCALE SHAPES;
D O I
10.1002/smll.201300701
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A convenient PCR cloning strategy allows one to prepare hundreds of picomoles of circular single-stranded DNA molecules, which are suitable as scaffolds for the assembly of DNA origami structures. The method is based on a combination of site-directed mutagenesis and site- and ligation-independent cloning protocols, with simultaneous insertion of a nicking endonuclease restriction site on a double-stranded plasmid of desired length and sequence. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:73 / 77
页数:5
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