Authors
Pedro Beltran-Alvarez, Ferran Feixas, Sílvia Osuna, Rubí Díaz-Hernández, Ramon Brugada, Sara Pagans
Publication date
2015/2
Journal
Amino acids
Volume
47
Pages
429-434
Publisher
Springer Vienna
Description
Arginine methylation is a novel post-translational modification within the voltage-gated ion channel superfamily, including the cardiac sodium channel, NaV1.5. We show that NaV1.5 R513 methylation decreases S516 phosphorylation rate by 4 orders of magnitude, the first evidence of protein kinase A inhibition by arginine methylation. Reciprocally, S516 phosphorylation blocks R513 methylation. NaV1.5 p.G514C, associated to cardiac conduction disease, abrogates R513 methylation, while leaving S516 phosphorylation rate unchanged. This is the first report of methylation–phosphorylation cross-talk of a cardiac ion channel.
Total citations
20152016201720182019202020212022202323134744