Localization of the two tropomyosin-binding sites of troponin T

被引:85
作者
Jin, J. -P. [1 ]
Chong, Stephen M. [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Physiol, Detroit, MI 48201 USA
基金
美国国家卫生研究院;
关键词
Troponin T; Tropomyosin; Striated muscle; Thin filament structure and regulation; NH2-TERMINAL VARIABLE REGION; RABBIT SKELETAL TROPONIN; CARDIAC TROPONIN; ALPHA-TROPOMYOSIN; FUNCTIONAL ADAPTATION; TERMINAL TRUNCATION; MUSCLE; FRAGMENTS; DELETION; SENSITIVITY;
D O I
10.1016/j.abb.2010.06.001
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
Troponin T (TnT) binds to tropomyosin (Tm) to anchor the troponin complex in the thin filament, and it thus serves as a vital link in the Ca2+ regulation of striated muscle contraction. Pioneer work three decades ago determined that the T1 and T2 chymotryptic fragments of TnT each contains a Tm-binding site. A more precise localization of the two Tm-binding sites of TnT remains to be determined. In the present study, we tested serial deletion constructs of TnT and carried out monoclonal antibody competition experiments to show that the T1 region Tm-binding site involves mainly a 39 amino acids segment in the N-terminal portion of the conserved middle region of TnT. We further employed another set of TnT fragments to locate the T2 region Tm-binding site to a segment of 25 amino acids near the beginning of the T2 fragment. The localization of the two Tm-binding sites of TnT provided new information for the structure-function relationship of TnT and the anchoring of troponin complex on muscle thin filament. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:144 / 150
页数:7
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