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基于力偶联酶反应的强韧和可还原的共价双网络水凝胶。

Strong and Reversible Covalent Double Network Hydrogel Based on Force-Coupled Enzymatic Reactions.

机构信息

Collaborative Innovation Center of Advanced Microstructures, National Laboratory of Solid State Microstructure, Key Laboratory of Intelligent Optical Sensing and Manipulation, Ministry of Education, Department of Physics, Nanjing University, Nanjing, 210093, China.

Jinan Microecological Biomedicine Shandong Laboratory, Jinan, 250021, China.

出版信息

Angew Chem Int Ed Engl. 2022 Jun 20;61(25):e202201765. doi: 10.1002/anie.202201765. Epub 2022 Apr 28.

Abstract

Biological load-bearing tissues are strong, tough, and recoverable under periodic mechanical loads. However, such features have rarely been achieved simultaneously in the same synthetic hydrogels. Here, we use a force-coupled enzymatic reaction to tune a strong covalent peptide linkage to a reversible bond. Based on this concept we engineered double network hydrogels that combine high mechanical strength and reversible mechanical recovery in the same hydrogels. Specifically, we found that a peptide ligase, sortase A, can promote the proteolysis of peptides under force. The peptide bond can be re-ligated by the same enzyme in the absence of force. This allows the sacrificial network in the double-network hydrogels to be ruptured and rebuilt reversibly. Our results demonstrate a general approach for precisely controlling the mechanical and dynamic properties of hydrogels at the molecular level.

摘要

生物承载组织具有较强的机械性能、韧性和在周期性机械负载下的可恢复性。然而,在同一合成水凝胶中同时实现这些特性的情况很少见。在这里,我们使用力偶联的酶反应来调节强共价肽键到可逆键。基于这一概念,我们设计了双重网络水凝胶,将高强度和可重复机械恢复结合在同一水凝胶中。具体来说,我们发现一种肽连接酶,即 sortase A,可以在力的作用下促进肽的蛋白水解。在没有力的情况下,相同的酶可以重新连接肽键。这使得双网络水凝胶中的牺牲网络可以可逆地断裂和重建。我们的结果证明了一种在分子水平上精确控制水凝胶力学和动态特性的通用方法。

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