Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Arch Biochem Biophys. 2010 Aug 15;500(2):144-50. doi: 10.1016/j.abb.2010.06.001. Epub 2010 Jun 8.
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 Ca(2+) 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.
肌钙蛋白 T(TnT)与原肌球蛋白(Tm)结合,将肌钙蛋白复合物锚定在细肌丝上,因此它是横纹肌收缩钙离子调节的重要环节。三十年前的开创性工作确定 TnT 的 T1 和 T2 糜蛋白酶片段都包含一个 Tm 结合位点。然而,TnT 的两个 Tm 结合位点的更精确定位仍有待确定。在本研究中,我们测试了 TnT 的串联缺失构建体,并进行了单克隆抗体竞争实验,结果表明 T1 区域 Tm 结合位点主要涉及 TnT 保守中间区域 N 端部分的 39 个氨基酸片段。我们进一步使用另一组 TnT 片段将 T2 区域 Tm 结合位点定位到 T2 片段起始附近的 25 个氨基酸片段上。TnT 两个 Tm 结合位点的定位为 TnT 的结构-功能关系以及肌钙蛋白复合物在肌肉细肌丝上的锚定提供了新的信息。