Department of Science, Mount St. Mary's University, Emmitsburg, MD, USA.
Methods Mol Biol. 2022;2444:271-282. doi: 10.1007/978-1-0716-2063-2_16.
Ubiquitylation is a posttranslational modification that utilizes protein-protein binding interactions to regulate cellular processes. In ubiquitin signaling, a vast array of mono- and polyubiquitin modifications to substrate proteins are recognized by a diverse group of ubiquitin-binding proteins. Identifying ubiquitin-binding proteins and characterizing their binding properties is necessary for understanding the structural basis of ubiquitin signaling. This chapter provides a means of studying ubiquitin-binding interactions in vitro by describing how to generate monoubiquitin and K63-linked polyubiquitin chains and perform pull-down assays with ubiquitin-binding proteins, which is of particular relevance for DNA damage and other signaling pathways.
泛素化是一种翻译后修饰,利用蛋白质-蛋白质结合相互作用来调节细胞过程。在泛素信号中,大量的单泛素和多泛素修饰底物蛋白被多种泛素结合蛋白识别。鉴定泛素结合蛋白并描述其结合特性是理解泛素信号结构基础的必要条件。本章提供了一种在体外研究泛素结合相互作用的方法,描述了如何生成单泛素和 K63 连接的多泛素链,并与泛素结合蛋白进行下拉实验,这对于 DNA 损伤和其他信号通路尤为重要。