| Literature DB >> 30791173 |
Yangyang Yang1, Shiwei Zhang1, Shengtao Yao1, Rizhao Pan1, Kumi Hidaka2, Tomoko Emura2, Chunhai Fan3, Hiroshi Sugiyama2, Yufang Xu1, Masayuki Endo2, Xuhong Qian1,4.
Abstract
Biological macromolecular machines perform impressive mechanical movements. F-adenosine triphosphate (ATP) synthase uses a proton gradient to generate ATP through mechanical rotations. Here, a programmed hexagonal DNA nanomachine, in which a three-armed DNA nanostructure (TAN) can perform stepwise rotations in the confined nanospace powered by DNA fuels, is demonstrated. The movement of TAN can precisely go through a 60° rotation, which is confirmed by atomic force microscopy, and each stepwise directional rotating is monitored by fluorescent measurements. Moreover, the rotary nanomachine is used to spatially organize cascade enzymes: glucose oxidase (GOx) and horseradish peroxidase (HRP) in four different arrangements. The multistep regulations of the biocatalytic activities are achieved by employing TAN rotations. This work presents a new prototype of rotary nanodevice with both angular and directional control, and provides a nanoscale mechanical engineering platform for the reactive molecular components, demonstrating that DNA-based framework may have significant roles in futuristic nanofactory construction.Entities:
Keywords: DNA origami; biocatalytic cascade reactions; nanodevices; rotary nanomachines
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Year: 2019 PMID: 30791173 DOI: 10.1002/chem.201900221
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236