School of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan, Hubei, China.
School of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan, Hubei, China.
Int J Biol Macromol. 2020 Nov 15;163:2127-2133. doi: 10.1016/j.ijbiomac.2020.09.058. Epub 2020 Sep 16.
Along with advancements in both protein and chemistry science, the chemical modification of proteins is attracting more and more attention. More specifically, the attachment of polymers or reactive moieties into collagen offers a method to add novel functions to this protein. However, the fibrillogenesis of the modified collagen with high grafting density cannot always be achieved. Here, inspired by the hybrid fibrils of xenogeneic collagen, fibrillogenesis of acrylic acid-grafted-collagen (AAc-g-Col) without self-assembly property was achieved by the induction of natural collagen (Col). The step-by-step co-assembly process of AAc-g-Col and Col was confirmed by turbidity assay. The formation of Col/AAc-g-Col hybrid fibrils was verified by TEM since the acryloyl groups of the hybrid fibrils were labelled using HS-AuNPs based on the Michael addition. Moreover, rheology, SEM, and MTT assays revealed that the fibrillary structures and biocompatibility of the Col/AAc-g-Col hydrogel were comparable to that of the Col hydrogel, although they presented a lower viscoelasticity.
随着蛋白质科学和化学科学的进步,蛋白质的化学修饰越来越受到关注。更具体地说,将聚合物或反应性部分附着到胶原蛋白上为这种蛋白质提供了添加新功能的方法。然而,具有高接枝密度的改性胶原的原纤维形成并不总是能够实现。在这里,受异种胶原蛋白混合原纤维的启发,通过天然胶原蛋白(Col)的诱导,实现了没有自组装性能的丙烯酸接枝胶原蛋白(AAc-g-Col)的原纤维形成。通过浊度测定证实了 AAc-g-Col 和 Col 的逐步共组装过程。通过 TEM 验证了 Col/AAc-g-Col 杂化原纤维的形成,因为杂化原纤维的丙烯酰基基团是基于迈克尔加成用 HS-AuNPs 标记的。此外,流变学、SEM 和 MTT 分析表明,尽管 Col/AAc-g-Col 水凝胶的粘弹性较低,但 Col/AAc-g-Col 水凝胶的纤维状结构和生物相容性与 Col 水凝胶相当。