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首页> 外文期刊>Journal of Muscle Research and Cell Motility >Cardiac myosin binding protein C phosphorylation in cardiac disease
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Cardiac myosin binding protein C phosphorylation in cardiac disease

机译:心脏疾病中心肌肌球蛋白结合蛋白C磷酸化

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Perturbations in sarcomeric function may in part underlie systolic and diastolic dysfunction of the failing heart. Sarcomeric dysfunction has been ascribed to changes in phosphorylation status of sarcomeric proteins caused by an altered balance between intracellular kinases and phosphatases during the development of cardiac disease. In the present review we discuss changes in phosphorylation of the thick filament protein myosin binding protein C (cMyBP-C) reported in failing myocardium, with emphasis on phosphorylation changes observed in familial hypertrophic cardiomyopathy caused by mutations in MYBPC3. Moreover, we will discuss assays which allow to distinguish between functional consequences of mutant sarcomeric proteins and (mal)adaptive changes in sarcomeric protein phosphorylation.
机译:肌节功能的紊乱可能部分归因于心脏衰竭的收缩和舒张功能障碍。肌节功能障碍归因于心脏病发展过程中细胞内激酶和磷酸酶之间平衡的改变引起的肌节蛋白磷酸化状态的改变。在本综述中,我们讨论了在衰竭心肌中报道的粗丝蛋白肌球蛋白结合蛋白C(cMyBP-C)磷酸化的变化,重点是在MYBPC3突变引起的家族性肥厚型心肌病中观察到的磷酸化变化。此外,我们将讨论允许区分突变型肌节蛋白的功能性后果和肌节蛋白磷酸化的(不良)适应性变化的测定方法。

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