cAPK-phosphorylation controls the interaction of the regulatory domain of cardiac myosin binding protein C with myosin-S2 in an on-off fashion

• Published in: FEBS letters Vol. 453; no. 3; pp. 254 - 259
• Main Authors: Gruen, Mathias, Prinz, Heino, Gautel, Mathias
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 25-06-1999
• Subjects: Calorimetry; Carrier Proteins - metabolism; Centrifugation; Cyclic AMP-Dependent Protein Kinases - metabolism; Myocardium - metabolism; Myosin binding protein C; Myosin regulation; Myosin Subfragments - metabolism; Phosphorylation; Protein Binding; Protein interaction; Protein Isoforms; Phosphorylation; Myosin regulation; Protein interaction; Myosin binding protein C
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/S0014-5793(99)00727-9

Myosin binding protein C is a protein of the myosin filaments of striated muscle which is expressed in isoforms specific for cardiac and skeletal muscle. The cardiac isoform is phosphorylated rapidly upon adrenergic stimulation of myocardium by cAMP-dependent protein kinase, and together with the phosphorylation of troponin-I and phospholamban contributes to the positive inotropy that results from adrenergic stimulation of the heart. Cardiac myosin binding protein C is phosphorylated by cAMP-dependent protein kinase on three sites in a myosin binding protein C specific N-terminal domain which binds to myosin-S2. This interaction with myosin close to the motor domain is likely to mediate the regulatory function of the protein. Cardiac myosin binding protein C is a common target gene of familial hypertrophic cardiomyopathy and most mutations encode N-terminal subfragments of myosin binding protein C. The understanding of the signalling interactions of the N-terminal region is therefore important for understanding the pathophysiology of myosin binding protein C associated cardiomyopathy. We demonstrate here by cosedimentation assays and isothermal titration calorimetry that the myosin-S2 binding properties of the myosin binding protein C motif are abolished by cAMP-dependent protein kinase-mediated tris-phosphorylation, decreasing the S2 affinity from a
K
d of ≈5 μM to undetectable levels. We show that the slow and fast skeletal muscle isoforms are no cAMP-dependent protein kinase substrates and that the S2 interaction of these myosin binding protein C isoforms is therefore constitutively on. The regulation of cardiac contractility by myosin binding protein C therefore appears to be a ‘brake-off’ mechanism that will free a specific subset of myosin heads from sterical constraints imposed by the binding to the myosin binding protein C motif.