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快速骨骼肌激活的结构基础。

Structural Basis of Activation of Fast Skeletal Muscle.

机构信息

Department of Biochemistry, University of Alberta, Edmonton, AB T6G 2H7, Canada.

National High Field NMR Centre, University of Alberta, Edmonton, AB T6G 2E1, Canada.

出版信息

J Med Chem. 2021 Mar 25;64(6):3026-3034. doi: 10.1021/acs.jmedchem.0c01412. Epub 2021 Mar 11.

Abstract

Troponin regulates the calcium-mediated activation of skeletal muscle. Muscle weakness in diseases such as amyotrophic lateral sclerosis and spinal muscular atrophy occurs from diminished neuromuscular output. The first direct fast skeletal troponin activator, , amplifies the response of muscle to neuromuscular input. binds selectively and strongly to fast skeletal troponin, slowing the rate of calcium release and sensitizing muscle to calcium. We report the solution NMR structure of bound to a fast skeletal troponin C-troponin I chimera. The structure reveals that binds in a hydrophobic pocket between the regulatory domain of troponin C and the switch region of troponin I, which overlaps with that of Anapoe in the X-ray structure of skeletal troponin. Multiple interactions stabilize the troponin C-troponin I interface, increase the affinity of troponin C for the switch region of fast skeletal troponin I, and drive the equilibrium toward the active state.

摘要

肌钙蛋白调节骨骼肌的钙介导激活。肌萎缩侧索硬化症和脊髓性肌萎缩等疾病导致肌肉无力,其原因是神经肌肉输出减少。第一个直接的快速骨骼肌肌钙蛋白激活剂 ,增强了肌肉对神经肌肉输入的反应。 选择性和强烈地结合快速骨骼肌肌钙蛋白,减缓钙释放的速度,并使肌肉对钙敏感。我们报告了与快速骨骼肌肌钙蛋白 C-肌钙蛋白 I 嵌合体结合的 的溶液 NMR 结构。该结构显示 结合在肌钙蛋白 C 的调节域和肌钙蛋白 I 的开关区域之间的疏水性口袋中,与骨骼肌肌钙蛋白的 X 射线结构中的 Anapoe 重叠。多种相互作用稳定了肌钙蛋白 C-肌钙蛋白 I 界面,增加了肌钙蛋白 C 与快速骨骼肌肌钙蛋白 I 开关区域的亲和力,并促使平衡向活性状态转变。

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