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刺激响应性肽-透明质酸杂化水凝胶的折叠驱动自组装。

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

机构信息

Division of Molecular Physics, Department of Physics, Chemistry and Biology, Linköping University, SE-583 36, Linköping, Sweden.

Division of Molecular Surface Physics and Nanoscience, Department of Physics, Chemistry and Biology, Linköping University, SE-583 36, Linköping, Sweden.

出版信息

Sci Rep. 2017 Aug 1;7(1):7013. doi: 10.1038/s41598-017-06457-9.

Abstract

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 Zn-responsive peptide-hyaluronic acid hybrid synthesized using strain promoted click chemistry. Addition of Zn triggers folding of the peptides into a helix-loop-helix motif and dimerization into four-helix bundles, resulting in hydrogelation. Removal of the Zn 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.

摘要

蛋白质-金属离子相互作用在自然界中普遍存在,可以用于控制复杂超分子结构和材料的自组装。在这里,我们描述了一种可调谐的超分子水凝胶,它是通过使用应变促进点击化学合成的 Zn 响应肽-透明质酸杂合体制备的自组装获得的。添加 Zn 会触发肽折叠成螺旋-环-螺旋结构,并二聚化形成四螺旋束,从而形成水凝胶。螯合剂去除 Zn 会导致水凝胶迅速解体。通过将水解酶封装在凝胶中,可以对水凝胶的降解进行时间编程,从而为调节材料性能和释放封装物质提供了多种可能性。当使用活性氧物种的体外模型评估时,水凝胶还显示出潜在的抗氧化特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fd0/5539109/d5206648db5f/41598_2017_6457_Fig1_HTML.jpg

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