Modulation of cardiac troponin C function by the cardiac-specific n-terminus of troponin I: Influence of PKA phosphorylation and involvement in cardiomyopathies

被引:47
作者
Baryshnikova, Olga K. [1 ]
Li, Monica X. [1 ]
Sykes, Brian D. [1 ]
机构
[1] Univ Alberta, Dept Biochem, Edmonton, AB T6G 2H7, Canada
基金
加拿大健康研究院;
关键词
troponin C; troponin I; phosphorylation; PKA; cardiomyopathy mutations;
D O I
10.1016/j.jmb.2007.10.062
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
The cardiac-specific N-terminus of cardiac troponin I (cTnI) is known to modulate the activity of troponin upon phosphorylation with protein kinase A (PKA) by decreasing its Ca2+ affinity and increasing the relaxation rate of the thin filament. The molecular details of this modulation have not been elaborated to date. We have established that the N-terminus and the switch region of cTnI bind to cNTnC [the N-domain of cardiac troponin C (cTnC)] simultaneously and that the PKA signal is transferred via the cTRI N-terminus. modulating the cNTnC affinity toward cTnI(147-163) but not toward Ca2+,. The K-d of cNTnC for cTnI(147-163) was found to be 600 mu M in the presence of cTnI(1-29) and 370 mu M in the presence of cTnI(1-29)PP, which can explain the difference in muscle relaxation rates upon the phosphorylation with PKA in experiments with cardiac fibers. In the light of newly found mutations in cNTnC that are associated with cardiomyopathies, the important role played by the cTnI N-terminus in the development of heart disorders emerges. The mutants studied, L29Q (the N-domain of cTnC containing mutation L29Q) and E59D/D75Y (the N-domain of cTnC containing mutation E59D/D75Y), demonstrated unchanged Ca2+ affinity per se and in complex with the cTnI N-terminus (cTnI(1-29) and cTnI(1-29)PP). The affinity of L29Q and E59D/D75Y toward cTnI(147-163) was significantly perturbed, both alone and in complex with cTnI(1-29) and cTnI(1-29)PP, Which is likely to be responsible for the development of malfunctions. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:735 / 751
页数:17
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