Identification of a novel cAMP dependent protein kinase A phosphorylation site on the human cardiac calcium channel

被引:16
|
作者
Szappanos, Henrietta Cserne [1 ]
Muralidharan, Padmapriya [1 ]
Ingley, Evan [2 ,3 ,4 ]
Petereit, Jakob [5 ]
Millar, Harvey A. [5 ]
Hool, Livia C. [1 ,6 ]
机构
[1] Univ Western Australia, Sch Human Sci, Crawley, WA, Australia
[2] Univ Western Australia, Harry Perkins Inst Med Res, Nedlands, WA, Australia
[3] Univ Western Australia, Ctr Med Res, Nedlands, WA, Australia
[4] Murdoch Univ, Sch Vet & Life Sci, Murdoch, WA, Australia
[5] Univ Western Australia, ARC Ctr Excellence Plant Energy Biol, Crawley, WA, Australia
[6] Victor Chang Cardiac Res Inst, Darlinghurst, NSW, Australia
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
澳大利亚研究理事会; 英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
BETA-ADRENERGIC STIMULATION; CA(V)1.2 CHANNELS; ANCHORING PROTEINS; CA2+ CHANNEL; CARBOXYL-TERMINUS; REQUIRES; ALPHA(1C); SUBUNIT; PKA; DOMAIN;
D O I
10.1038/s41598-017-15087-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The "Fight or Flight" response is elicited by extrinsic stress and is necessary in many species for survival. The response involves activation of the beta-adrenergic signalling pathway. Surprisingly the mechanisms have remained unresolved. Calcium influx through the cardiac L-type Ca2+ channel (Ca(v)1.2) is absolutely required. Here we identify the functionally relevant site for PKA phosphorylation on the human cardiac L-type Ca2+ channel pore forming alpha 1 subunit using a novel approach. We used a cell free system where we could assess direct effects of PKA on human purified channel protein function reconstituted in proteoliposomes. In addition to assessing open probability of channel protein we used semi-quantitative fluorescent phosphoprotein detection and MS/MS mass spectrometry analysis to demonstrate the PKA specificity of the site. Robust increases in frequency of channel openings were recorded after phosphorylation of the long and short N terminal isoforms and the channel protein with C terminus truncated at aa1504. A protein kinase A anchoring protein (AKAP) was not required. We find the novel PKA phosphorylation site at Ser1458 is in close proximity to the Repeat IV S6 region and induces a conformational change in the channel protein that is necessary and sufficient for increased calcium influx through the channel.
引用
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页数:16
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