Short peptides that can respond to external stimuli have been considered as the preferred building blocks to construct hydrogels for biomedical applications. In particular, photoresponsive peptides that are capable of triggering the formation of hydrogels upon light irradiation allow the properties of hydrogels to be changed remotely by precise and localized actuation. Here, we used the photochemical reaction of the 2-nitrobenzyl ester group (NB) to develop a facile and versatile strategy for constructing photoactivated peptide hydrogels.
View Article and Find Full Text PDFPeptide-based supramolecular hydrogels have attracted great attention due to their good biocompatibility and biodegradability and have become promising candidates for biomedical applications. The bottom-up self-assembly endows the peptides with a highly ordered secondary structure, which has proven to be an effective strategy to improve the mechanical properties of hydrogels through strong physical interactions and energy dissipation. Inspired by the excellent mechanical properties of spider-silk, which can be attributed to the rich β-sheet crystal formation by the hydrophobic peptide fragment, a hydrophobic peptide (HP) that can form a β-sheet assembly was designed and introduced into a poly(vinyl alcohol) (PVA) scaffold to improve mechanical properties of hydrogels by the cooperative intermolecular physical interactions.
View Article and Find Full Text PDFRegulating cell-surface interactions plays a key role for biomaterials and their applications in cell-based therapies. In this paper, we demonstrated a dual-responsive hydrogel platform to achieve phototriggered protein immobilization and reduction-induced protein release. By -nitrobenzyl photochemistry, including sequential aldehyde generation upon light irradiation and imine ligation with amine compounds, adhesive proteins can be effectively immobilized on the hydrogel with spatial and quantitative control, thus mediating cell adhesion in designed areas.
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