Author
Listed:
- Bimalendu Adhikari
(Graduate School of Engineering, Chiba University
Indian Institute of Science Education and Research (IISER) Mohali, Knowledge City)
- Yuki Yamada
(Graduate School of Engineering, Chiba University)
- Mitsuaki Yamauchi
(Graduate School of Engineering, Chiba University)
- Kengo Wakita
(Graduate School of Engineering, Chiba University)
- Xu Lin
(Graduate School of Engineering, Chiba University)
- Keisuke Aratsu
(Graduate School of Engineering, Chiba University)
- Tomonori Ohba
(Graduate School of Science, Chiba University)
- Takashi Karatsu
(Graduate School of Engineering, Chiba University)
- Martin J. Hollamby
(School of Chemical and Physical Sciences, Keele University)
- Nobutaka Shimizu
(Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization)
- Hideaki Takagi
(Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization)
- Rie Haruki
(Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization)
- Shin-ichi Adachi
(Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization)
- Shiki Yagai
(Graduate School of Engineering, Chiba University)
Abstract
Unlike classical covalent polymers, one-dimensionally (1D) elongated supramolecular polymers (SPs) can be encoded with high degrees of internal order by the cooperative aggregation of molecular subunits, which endows these SPs with extraordinary properties and functions. However, this internal order has not yet been exploited to generate and dynamically control well-defined higher-order (secondary) conformations of the SP backbone, which may induce functionality that is comparable to protein folding/unfolding. Herein, we report light-induced conformational changes of SPs based on the 1D exotic stacking of hydrogen-bonded azobenzene hexamers. The stacking causes a unique internal order that leads to spontaneous curvature, which allows accessing conformations that range from randomly folded to helically folded coils. The reversible photoisomerization of the azobenzene moiety destroys or recovers the curvature of the main chain, which demonstrates external control over the SP conformation that may ultimately lead to biological functions.
Suggested Citation
Bimalendu Adhikari & Yuki Yamada & Mitsuaki Yamauchi & Kengo Wakita & Xu Lin & Keisuke Aratsu & Tomonori Ohba & Takashi Karatsu & Martin J. Hollamby & Nobutaka Shimizu & Hideaki Takagi & Rie Haruki & , 2017.
"Light-induced unfolding and refolding of supramolecular polymer nanofibres,"
Nature Communications, Nature, vol. 8(1), pages 1-10, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15254
DOI: 10.1038/ncomms15254
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