| Literature DB >> 33659327 |
William L Willis1, Abigail Foster1, Caitlin Henry1, Lai Chu Wu1, Wael Jarjour1.
Abstract
Transglutaminase (TG2) catalyzes protein crosslinking between glutamyl and lysyl residues. Catalytic activity occurs via a transamidation mechanism resulting in the formation of isopeptide bonds. Since TG2-mediated transamidation is of mechanistic importance for a number of biological processes, assays that enable rapid and efficient identification and characterization of candidate substrates are an important first-step to uncovering the function of crosslinked proteins. Herein we describe an optimized and flexible protocol for in vitro TG2 crosslink reactions and substrate incorporation assays. We have previously employed these techniques in the identification of the protein high mobility group box 1 (HMGB1) as a TG2 substrate. However, the protocol can be adapted for identification of any candidate transamidation substrate.Entities:
Keywords: High mobility group box 1; In vitro protein crosslinking ; Isopeptide; Post-translational modification; Transamidation; Transglutaminase
Year: 2020 PMID: 33659327 PMCID: PMC7842806 DOI: 10.21769/BioProtoc.3657
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325