| Literature DB >> 28199775 |
Yangyang Yang1,2,3, Ryu Tashiro4, Yuki Suzuki2,5, Tomoko Emura2, Kumi Hidaka2, Hiroshi Sugiyama1,2, Masayuki Endo1.
Abstract
Various DNA-based nanodevices have been developed on the nanometer scale using light as regulation input. However, the programmed controllability is still a major challenge for these artificial nanodevices. Herein, we demonstrate a rotary DNA nanostructure in which the rotations are controlled by light. A bar-shaped DNA rotor, fabricated as a stiff double-crossover molecule, was placed on the top of a rectangular DNA tile. The photoresponsive oligonucleotides modified with azobenzenes were employed as switching motifs to release/trap the rotor at specific angular position on DNA tile by switching photoirradiations between ultraviolet and visible light. As a result, two reconfigurable states (perpendicular and parallel) of rotor were obtained, in which the angular changes were characterized by AFM and fluorescence quenching assays. Moreover, the reversible rotary motions during the photoirradiation were directly visualized on the DNA tile surface in a nanometer-scale precision using a second-scale scanning of the high-speed AFM.Entities:
Keywords: DNA; high-speed AFM; molecular wires; nanotechnology; photochemistry
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Year: 2017 PMID: 28199775 DOI: 10.1002/chem.201605616
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236