| Literature DB >> 35290643 |
Rita Anoh1, Kate A Burke1, Dhane P Schmelyun1, Patrick M Lombardi2.
Abstract
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.Entities:
Keywords: Cellular signaling; Polyubiquitin chains; Pull-down assay; Ubiquitin; Ubiquitin-activating enzyme; Ubiquitin-binding protein; Ubiquitin-conjugating enzyme; Ubiquitin-conjugation reaction
Mesh:
Substances:
Year: 2022 PMID: 35290643 DOI: 10.1007/978-1-0716-2063-2_16
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745