Department of Biomedical and Molecular Sciences, Queen's University, Kingston K7L 3N6, Canada.
Department of Biomedical and Molecular Sciences, Queen's University, Kingston K7L 3N6, Canada.
STAR Protoc. 2024 Jun 21;5(2):102947. doi: 10.1016/j.xpro.2024.102947. Epub 2024 Mar 11.
Polyphosphate exhibits a unique post-translational modification-like function, known as histidine polyphosphate modification (HPM), marked by a robust non-covalent interaction with histidine repeat proteins. Here, we present a protocol for detecting HPM of human proteins via maltose-binding protein-tagged expression in E. coli. We describe steps for detecting HPM by observing electrophoretic mobility shifts on NuPAGE gels followed by western blot. We then detail procedures for analyzing the influence of ionic strength and pH on HPM. For complete details on the use and execution of this protocol, please refer to Neville et al..
多聚磷酸盐表现出一种独特的翻译后修饰样功能,称为组氨酸多聚磷酸盐修饰(HPM),其特征是与组氨酸重复蛋白之间存在强大的非共价相互作用。在这里,我们通过在大肠杆菌中用麦芽糖结合蛋白标记表达来展示一种检测人蛋白 HPM 的方案。我们描述了通过观察 NuPAGE 凝胶上的电泳迁移率变化,然后进行 Western blot 来检测 HPM 的步骤。然后,我们详细介绍了分析离子强度和 pH 对 HPM 影响的程序。有关此方案的使用和执行的完整详细信息,请参阅 Neville 等人的研究。