Walkup Ward G, Kennedy Mary B
Department of Biology and Biological Engineering, California Institute of Technology, Pasadena, California.
Curr Protoc Protein Sci. 2015 Apr 1;80:9.10.1-9.10.37. doi: 10.1002/0471140864.ps0910s80.
PDZ domains function in nature as protein-binding domains within scaffold and membrane-associated proteins. They comprise approximately 90 residues and undergo specific, high-affinity interactions with complementary C-terminal peptide sequences, other PDZ domains, and/or phospholipids. We have previously shown that the specific, strong interactions of PDZ domains with their ligands make them well suited for use in affinity chromatography. This unit provides protocols for the PDZ affinity chromatography procedure that are applicable for the purification of proteins that contain PDZ domains or PDZ domain-binding ligands, either naturally or introduced by genetic engineering. We detail the preparation of affinity resins composed of PDZ domains or PDZ domain peptide ligands coupled to solid supports. These resins can be used to purify proteins containing endogenous or genetically introduced PDZ domains or ligands, eluting the proteins with free PDZ domain peptide ligands.
PDZ结构域在自然界中作为支架蛋白和膜相关蛋白中的蛋白质结合结构域发挥作用。它们由大约90个氨基酸残基组成,并与互补的C末端肽序列、其他PDZ结构域和/或磷脂进行特异性的高亲和力相互作用。我们之前已经表明,PDZ结构域与其配体之间的特异性强相互作用使其非常适合用于亲和色谱法。本单元提供了PDZ亲和色谱法的实验方案,适用于纯化天然存在或通过基因工程引入的含有PDZ结构域或PDZ结构域结合配体的蛋白质。我们详细介绍了由与固体支持物偶联的PDZ结构域或PDZ结构域肽配体组成的亲和树脂的制备方法。这些树脂可用于纯化含有内源性或基因工程引入的PDZ结构域或配体的蛋白质,用游离的PDZ结构域肽配体洗脱蛋白质。