Lipid-bilayer-assisted two-dimensional self-assembly of DNA origami nanostructures

被引:174
作者
Suzuki, Yuki [1 ,2 ]
Endo, Masayuki [2 ,3 ]
Sugiyama, Hiroshi [1 ,2 ,3 ]
机构
[1] Kyoto Univ, Dept Chem, Grad Sch Sci, Sakyo Ku, Kyoto 6068502, Japan
[2] Japan Sci & Technol Agcy JST, CREST, Chiyoda Ku, Tokyo 1020075, Japan
[3] Kyoto Univ, Inst Integrated Cell Mat Sci WPI iCeMS, Sakyo Ku, Kyoto 6068501, Japan
关键词
ATOMIC-FORCE MICROSCOPY; BIOMOLECULAR PROCESSES; PHOSPHOLIPID-BILAYERS; MOLECULAR RECOGNITION; PATTERNED SURFACES; NANOSCALE SHAPES; FOLDING DNA; MEMBRANE; DIFFUSION; CRYSTALS;
D O I
10.1038/ncomms9052
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Self-assembly is a ubiquitous approach to the design and fabrication of novel supermolecular architectures. Here we report a strategy termed 'lipid-bilayer-assisted self-assembly' that is used to assemble DNA origami nanostructures into two-dimensional lattices. DNA origami structures are electrostatically adsorbed onto a mica-supported zwitterionic lipid bilayer in the presence of divalent cations. We demonstrate that the bilayer-adsorbed origami units are mobile on the surface and self-assembled into large micrometre-sized lattices in their lateral dimensions. Using high-speed atomic force microscopy imaging, a variety of dynamic processes involved in the formation of the lattice, such as fusion, reorganization and defect filling, are successfully visualized. The surface modifiability of the assembled lattice is also demonstrated by in situ decoration with streptavidin molecules. Our approach provides a new strategy for preparing versatile scaffolds for nanofabrication and paves the way for organizing functional nanodevices in a micrometer space.
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页数:9
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