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Folding driven self-assembly of a stimuli-responsive peptide-hyaluronan hybrid hydrogel

机译:折叠响应的刺激响应肽-透明质酸杂化水凝胶的自组装

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摘要

Protein-metal ion interactions are ubiquitous in nature and can be utilized for controlling the self-assembly of complex supramolecular architectures and materials. Here, a tunable supramolecular hydrogel is described, obtained by self-assembly of a Zn2+-responsive peptide-hyaluronic acid hybrid synthesized using strain promoted click chemistry. Addition of Zn2+ triggers folding of the peptides into a helix-loop-helix motif and dimerization into four-helix bundles, resulting in hydrogelation. Removal of the Zn2+ by chelators results in rapid hydrogel disassembly. Degradation of the hydrogels can also be time-programed by encapsulation of a hydrolyzing enzyme within the gel, offering multiple possibilities for modulating materials properties and release of encapsulated species. The hydrogel further shows potential antioxidant properties when evaluated using an in vitro model for reactive oxygen species.
机译:蛋白质-金属离子相互作用本质上是普遍存在的,可用于控制复杂的超分子结构和材料的自组装。在这里,描述了一种可调谐的超分子水凝胶,它是通过自组装使用应变促进点击化学方法合成的Zn 2 + 响应肽-透明质酸杂交体而获得的。 Zn 2 + 的添加触发了肽折叠成螺旋-环-螺旋基序并二聚为四螺旋束,从而导致水凝胶化。螯合剂去除Zn 2 + 导致水凝胶快速分解。水凝胶的降解还可以通过将水解酶封装在凝胶中来进行时间编程,从而为调节材料特性和释放被封装物质提供了多种可能性。当使用活性氧的体外模型评估时,水凝胶进一步显示出潜在的抗氧化性能。

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