Photo Gel-Sol/Sol-Gel Transition and Its Patterning of a Supramolecular Hydrogel as Stimuli-Responsive Biomaterials

In a focused library of glycolipid‐based hydrogelators bearing fumaric amide as a trans–cis photoswitching module, several new photoresponsive supramolecular hydrogelators were discovered, the gel–sol/sol–gel transition of which was pseudo‐reversibly induced by light. Studying the optimal hydrogel b...

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Published in:Chemistry : a European journal 2008-04, Vol.14 (13), p.3977-3986
Main Authors: Matsumoto, Shinji, Yamaguchi, Satoshi, Ueno, Shiori, Komatsu, Harunobu, Ikeda, Masato, Ishizuka, Koji, Iko, Yuko, Tabata, Kazuhito V., Aoki, Hiroyuki, Ito, Shinzaburo, Noji, Hiroyuki, Hamachi, Itaru
Format: Article
Language:English
Subjects:
Biocompatible Materials - chemistry
Escherichia coli - cytology
gels
Glycolipids - chemistry
Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry
immobilization
Microscopy, Electron, Scanning
Microscopy, Electron, Transmission
Molecular Structure
Nanostructures - chemistry
Phase Transition
Photochemistry
Proton-Translocating ATPases - metabolism
self-assembly
Sensitivity and Specificity
supramolecular chemistry
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Summary:In a focused library of glycolipid‐based hydrogelators bearing fumaric amide as a trans–cis photoswitching module, several new photoresponsive supramolecular hydrogelators were discovered, the gel–sol/sol–gel transition of which was pseudo‐reversibly induced by light. Studying the optimal hydrogel by NMR spectroscopy and various microscopy techniques showed that the trans–cis photoisomerization of the double bond of the fumaric amide unit effectively caused assembly or disassembly of the self‐assembled supramolecular fibers to yield the macroscopic hydrogel or the corresponding sol, respectively. The entanglement of the supramolecular fibers produced nanomeshes, the void space of which was roughly evaluated to be 250 nm based on confocal laser scanning microscopy observations of the size‐dependent Brownian motion of nanobeads embedded in the supramolecular hydrogel. It was clearly shown that such nanomeshes become a physical obstacle that captures submicro‐ to micrometer‐sized substrates such as beads or bacteria. By exploiting the photoresponsive property of the supramolecular nanomeshes, we succeeded in off/on switching of bacterial movement and rotary motion of bead‐tethered F1‐ATPase, a biomolecular motor protein, in the supramolecular hydrogel. Furthermore, by using the photolithographic technique, gel–sol photopatterning was successfully conducted to produce sol spots within the gel matrix. The fabricated gel–sol pattern not only allowed regulation of bacterial motility in a limited area, but also off/on switching of F1‐ATPase rotary motion at the single‐molecule level. These results demonstrated that the photoresponsive supramolecular hydrogel and the resulting nanomeshes may provide unique biomaterials for the spatiotemporal manipulation of various biomolecules and live bacteria. Caught in the mesh: Several photoresponsive supramolecular hydrogelators were designed, the gel–sol and sol–gel transitions of which are pseudo‐reversibly induced by UV irradiation and visible irradiation in the presence of Br2. The accompanying disassembly and assembly of supramolecular meshes of gel fibers can be used for on–off switching of bacterial movement (see scheme) and of the rotary motion of bead‐tethered F1‐ATPase, a biomolecular motor protein.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.200701904