Division of Protein Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH/AlbaNova University Center, Stockholm, Sweden.
Department of Protein Science, KTH Royal Institute of Technology, School of Engineering Sciences in Chemistry Biotechnology and Health (CBH), AlbaNova University Center, Stockholm, Sweden.
Methods Mol Biol. 2021;2178:159-166. doi: 10.1007/978-1-0716-0775-6_13.
In this chapter, we present an efficient method for stringent protein purification facilitated by a dual affinity tag referred to as ABDz1, which is based on a 5 kDa albumin-binding domain from Streptococcal Protein G. The small fusion tag enables an orthogonal affinity purification approach based on two successive and highly specific affinity purification steps. This approach is enabled by native binding of ABDz1 to human serum albumin and engineered binding to Staphylococcal Protein A, respectively. The ABDz1-tag can be fused to either terminus of a protein of interest and the purification steps can be carried out using standard laboratory equipment.
在本章中,我们提出了一种通过双亲和标签(称为 ABDz1)实现严格蛋白质纯化的有效方法,该标签基于来自链球菌蛋白 G 的 5 kDa 白蛋白结合结构域。该小融合标签支持基于两个连续且高度特异性亲和纯化步骤的正交亲和纯化方法。该方法分别通过 ABDz1 与人血清白蛋白的天然结合和与葡萄球菌蛋白 A 的工程结合来实现。ABDz1 标签可融合到目标蛋白的任一端,并且可以使用标准实验室设备进行纯化步骤。