Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong SAR, People's Republic of China.
Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong SAR, People's Republic of China.
Methods Enzymol. 2021;647:283-301. doi: 10.1016/bs.mie.2020.09.011. Epub 2020 Oct 14.
The peptide/protein pair, SpyTag/SpyCatcher, which is derived from split immunoglobulin-like collagen adhesin domain (CnaB2) from Streptococcus pyogenes, can spontaneously form a stable Lys-Asp isopeptide bond under physiological conditions. This enabling technology- also known as genetically encoded click chemistry owing to its marked efficiency and specificity-has led to a variety of applications in protein engineering, materials science and synthetic biology in recent years. In this chapter, we discuss the use of SpyTag/SpyCatcher chemistry to create nonlinear protein architectures and materials, with emphasis on its role in shaping up topology engineering as an emerging branch of protein engineering. The synthesis of entirely protein-based molecular networks, Spy networks, is highlighted. The protocols for preparing Spy networks and applications thereof are also illustrated.
SpyTag/SpyCatcher 肽/蛋白对来源于酿脓链球菌(Streptococcus pyogenes)的分裂免疫球蛋白样胶原黏附结构域(CnaB2),可在生理条件下自发形成稳定的赖氨酸-天冬氨酸异肽键。这项被称为基因编码点击化学的技术,由于其显著的效率和特异性,近年来在蛋白质工程、材料科学和合成生物学领域得到了广泛的应用。在本章中,我们讨论了使用 SpyTag/SpyCatcher 化学来构建非线性蛋白质结构和材料,重点介绍了它在作为蛋白质工程新兴分支的拓扑工程中的作用。我们还强调了完全基于蛋白质的分子网络 Spy 网络的合成。此外,还说明了制备 Spy 网络的方案及其应用。