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Updated: Jun 4, 2026

Preparation of Mechanically Stable Self-Assembled Peptides Hydrogels
Published on: September 6, 2024
Modular Molecular Design and Self-Assembled Nanostructures of Saccharide‑Appended Cyclic Dipeptides for
Shintaro Sugiura1, Ryuta Tanaka2, Sayuri L Higashi1,3,4
1United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, Gifu, Japan.
Abstract:
Glycosidase-responsive supramolecular hydrogels represent a promising class of soft materials for biomedical applications, as glycosidases play pivotal roles in various physiological processes and viral infections. In this study, saccharide-appended cyclic dipeptides are designed as modular building blocks for the construction of supramolecular hydrogel systems through aqueous self-assembly. Notably, β-galactosidase-responsive gel-to-sol and neuraminidase (sialidase)-responsive sol-to-gel transitions are achieved by employing cyclic dipeptides appended with galactose and N-acetylneuraminic acid, respectively, under appropriate formulations.

