R-catcher, a potent molecular tool to unveil the arginylome

Author:

Seo Taewook,Kim Jihyo,Shin Ho-Chul,Kim Jung Gi,Ju Shinyeong,Nawale Laxman,Han Goeun,Lee Hye Seon,Bang Geul,Kim Jin Young,Bang Jeong Kyu,Lee Kyung Ho,Soung Nak-Kyun,Hwang Joonsung,Lee Cheolju,Kim Seung Jun,Kim Bo Yeon,Cha-Molstad HyunjooORCID

Abstract

AbstractProtein 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.

Funder

National Research Council of Science and Technology

Ministry of Science, ICT and Future Planning

Korea Research Institute of Bioscience and Biotechnology

National Research Foundation of Korea

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine

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