Protein arginylation is a critical regulator of a variety of biological processes. The ability to uncover the global arginylation pattern and its associated signaling pathways would enable us to identify novel disease targets. Here, we report the development of a tool able to capture the N-terminal arginylome. This tool, termed R-catcher, is based on the ZZ domain of p62, which was previously shown to bind N-terminally arginylated proteins. Mutating the ZZ domain enhanced its binding specificity and affinity for Nt-Arg. R-catcher pulldown coupled to LC-MS/MS led to the identification of 59 known and putative arginylated proteins. Among these were a subgroup of novel ATE1-dependent arginylated ER proteins that are linked to diverse biological pathways, including cellular senescence and vesicle-mediated transport as well as diseases, such as Amyotrophic Lateral Sclerosis and Alzheimer’s disease. This study presents the first molecular tool that allows the unbiased identification of arginylated proteins, thereby unlocking the arginylome and provide a new path to disease biomarker discovery.
About The Expert
Taewook Seo
Jihyo Kim
Ho-Chul Shin
Jung Gi Kim
Shinyeong Ju
Laxman Nawale
Goeun Han
Hye Seon Lee
Geul Bang
Jin Young Kim
Jeong Kyu Bang
Kyung Ho Lee
Nak-Kyun Soung
Joonsung Hwang
Cheolju Lee
Seung Jun Kim
Bo Yeon Kim
Hyunjoo Cha-Molstad
References
PubMed