Interplay between R513 methylation and S516 phosphorylation of the cardiac voltage-gated sodium channel

被引:20
作者
Beltran-Alvarez, Pedro [1 ,2 ]
Feixas, Ferran [3 ,4 ]
Osuna, Silvia [3 ,4 ]
Diaz-Hernandez, Rubi [1 ,2 ]
Brugada, Ramon [1 ,2 ]
Pagans, Sara [1 ,2 ]
机构
[1] Univ Girona, Inst Invest Biomed Girona Dr Josep Trueta, Cardiovasc Genet Ctr, Girona 17003, Spain
[2] Univ Girona, Sch Med, Dept Med Sci, Girona 17003, Spain
[3] Univ Girona, IQCC, Girona 17071, Spain
[4] Univ Girona, Dept Quim, Girona 17071, Spain
关键词
Sodium channel; Post-translational modification; Arginine methylation; Phosphorylation; Cross-talk; ARGININE METHYLATION; MASS-SPECTROMETRY; PROTEIN; METHYLTRANSFERASE; IDENTIFICATION;
D O I
10.1007/s00726-014-1890-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Arginine methylation is a novel post-translational modification within the voltage-gated ion channel superfamily, including the cardiac sodium channel, Na(V)1.5. We show that Na(V)1.5 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. Na(V)1.5 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.
引用
收藏
页码:429 / 434
页数:6
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