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非键相互作用对丝素蛋白水凝胶凝胶化机制作用的研究。

Investigations into the role of non-bond interaction on gelation mechanism of silk fibroin hydrogel.

作者信息

Jiang Xuewei, Zheng Lu, Zeng Jing, Wu Huhe, Zhang Jun

机构信息

Wuhan Textile and Apparel Digital Engineering Technology Research Center, Wuhan Textile University, Wuhan 430073, China.

出版信息

Math Biosci Eng. 2021 May 10;18(4):4071-4083. doi: 10.3934/mbe.2021204.

Abstract

Silk fibroin hydrogel not only has biocompatibility, but also has environmental response ability. It plays an important role in the development of material. The gelation mechanism of silk fibroin hydrogel is very important to textile and medicine fields. The molecular dynamics simulation was used to discuss the structure and non-bond interaction of silk fibroin hydrogel. The results show that the non-bond interactions between silk fibroin molecules and water molecules have certain influence on the formation of silk fibroin hydrogel. According to the hydrogen bond analysis, the hydrogen bonds are mainly formed between random coil peptide fragments at the two ends of silk fibroin molecules and residues 252-254 are the key residues. The electrostatic and polar solvation interactions between silk fibroin molecules plays a major role in cross-linking of the coil segments of two silk fibroin molecules.

摘要

丝素蛋白水凝胶不仅具有生物相容性,还具有环境响应能力。它在材料发展中起着重要作用。丝素蛋白水凝胶的凝胶化机制对纺织和医学领域非常重要。利用分子动力学模拟来探讨丝素蛋白水凝胶的结构和非键相互作用。结果表明,丝素蛋白分子与水分子之间的非键相互作用对丝素蛋白水凝胶的形成有一定影响。根据氢键分析,氢键主要在丝素蛋白分子两端的无规卷曲肽片段之间形成,且残基252 - 254是关键残基。丝素蛋白分子之间的静电和极性溶剂化相互作用在两个丝素蛋白分子的卷曲片段交联中起主要作用。

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