| Literature DB >> 35419931 |
Guangxiao He1,2,3, Hai Lei1, Wenxu Sun3, Jie Gu1, Wenting Yu1, Di Zhang1, Huiyan Chen1, Ying Li4, Meng Qin1, Bin Xue1, Wei Wang1, Yi Cao1,5,6.
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.Entities:
Keywords: Double-Network Hydrogels; Dynamic Covalent Bonds; Force-Coupled Enzymatic Reaction; Mechanical Properties; Single-Molecule Force Spectroscopy
Mesh:
Substances:
Year: 2022 PMID: 35419931 DOI: 10.1002/anie.202201765
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336