Centre for Engineering Biology, Institute of Quantitative Biology, Biochemistry and Biotechnology, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Edinburgh Protein Production Facility (EPPF), University of Edinburgh, Edinburgh, United Kingdom.
J Struct Biol. 2023 Sep;215(3):107981. doi: 10.1016/j.jsb.2023.107981. Epub 2023 May 26.
Biomaterials for tissue regeneration must mimic the biophysical properties of the native physiological environment. A protein engineering approach allows the generation of protein hydrogels with specific and customised biophysical properties designed to suit a particular physiological environment. Herein, repetitive engineered proteins were successfully designed to form covalent molecular networks with defined physical characteristics able to sustain cell phenotype. Our hydrogel design was made possible by the incorporation of the SpyTag (ST) peptide and multiple repetitive units of the SpyCatcher (SC) protein that spontaneously formed covalent crosslinks upon mixing. Changing the ratios of the protein building blocks (ST:SC), allowed the viscoelastic properties and gelation speeds of the hydrogels to be altered and controlled. The physical properties of the hydrogels could readily be altered further to suit different environments by tuning the key features in the repetitive protein sequence. The resulting hydrogels were designed with a view to allow cell attachment and encapsulation of liver derived cells. Biocompatibility of the hydrogels was assayed using a HepG2 cell line constitutively expressing GFP. The cells remained viable and continued to express GFP whilst attached or encapsulated within the hydrogel. Our results demonstrate how this genetically encoded approach using repetitive proteins could be applied to bridge engineering biology with nanotechnology creating a level of biomaterial customisation previously inaccessible.
用于组织再生的生物材料必须模拟天然生理环境的生物物理特性。蛋白质工程方法允许生成具有特定和定制生物物理特性的蛋白质水凝胶,以适应特定的生理环境。在此,通过重复设计的工程蛋白质成功地形成了具有定义物理特性的共价分子网络,能够维持细胞表型。我们的水凝胶设计得益于 SpyTag (ST) 肽和多个 SpyCatcher (SC) 蛋白重复单元的掺入,它们在混合时会自发形成共价交联。改变蛋白质构建块(ST:SC)的比例,可以改变和控制水凝胶的粘弹性和凝胶速度。通过调整重复蛋白质序列中的关键特征,可以进一步改变水凝胶的物理性质以适应不同的环境。所得到的水凝胶旨在允许细胞附着和封装肝脏来源的细胞。使用持续表达 GFP 的 HepG2 细胞系来测定水凝胶的生物相容性。当细胞附着或封装在水凝胶内时,细胞保持存活并继续表达 GFP。我们的结果表明,如何使用重复蛋白质的这种基因编码方法可以将工程生物学与纳米技术联系起来,从而创造出以前无法实现的生物材料定制水平。