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

Authors
Seo, TaewookKim, JihyoShin, Ho-ChulKim, Jung GiJu, ShinyeongNawale, LaxmanHan, GoeunLee, Hye SeonBang, GeulKim, Jin YoungBang, Jeong KyuLee, Kyung HoSoung, Nak-KyunHwang, JoonsungLee, CheoljuKim, Seung JunKim, Bo YeonCha-Molstad, Hyunjoo
Issue Date
2021-04
Publisher
SPRINGER BASEL AG
Citation
CELLULAR AND MOLECULAR LIFE SCIENCES, v.78, no.7, pp.3725 - 3741
Abstract
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.
Keywords
ATE1 R-transferase; Bait; FBLN1; CLUS; SERPINH1; PRDX4; Unfolded Protein Response; Extracellular exosome; Innate Immune System; Prostate cancer; Ovarian cancer
ISSN
1420-682X
URI
https://pubs.kist.re.kr/handle/201004/117182
DOI
10.1007/s00018-021-03805-x
Appears in Collections:
KIST Article > 2021
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