Specific association of calmodulin-dependent protein kinase and related substrates with the junctional sarcoplasmic reticulum of skeletal muscle

• Published in: Biochemistry (Easton) Vol. 29; no. 25; pp. 5899 - 5905
• Main Authors: Chu, Alice, Sumbilla, Carlota, Inesi, Giuseppe, Jay, Scott D, Campbell, Kevin P
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 26.06.1990
• Subjects: Adenosine Triphosphate - metabolism; Animals; Autoradiography; Biological and medical sciences; Blotting, Western; Calcineurin; Calcium - metabolism; Calcium - pharmacology; Calcium Channels - metabolism; calmodulin; Calmodulin - metabolism; Calmodulin - pharmacology; Calmodulin-Binding Proteins - pharmacology; Electrophoresis, Polyacrylamide Gel; Fundamental and applied biological sciences. Psychology; Interactions. Associations; Intermolecular phenomena; Kinetics; Microsomes - enzymology; Molecular biophysics; Muscles - enzymology; Muscles - ultrastructure; Phosphoprotein Phosphatases - pharmacology; Phosphorylation; protein kinase; Protein Kinases - metabolism; Protein Phosphatase 1; Rabbits; Receptors, Cholinergic - metabolism; Ryanodine - metabolism; Ryanodine Receptor Calcium Release Channel; sarcoplasmic reticulum; Sarcoplasmic Reticulum - enzymology; Time Factors; Phosphorylation; Enzymatic activity; Calcium; Gel electrophoresis; Protein kinase; Sarcoplasmic reticulum; Membrane transport; Molecular interaction; Muscle; ATP; Calmodulin
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00477a003

A systematic study of protein kinase activity and phosphorylation of membrane proteins by ATP was carried out with vesicular fragments of longitudinal tubules (light SR) and junctional terminal cisternae (JTC) derived from skeletal muscle sarcoplasmic reticulum (SR). Following incubation of JTC with ATP, a 170,000-Da glycoprotein, a 97,500-Da protein (glycogen phosphorylase), and a 55,000-60,000-Da doublet (containing calmodulin-dependent protein kinase subunit) underwent phosphorylation. Addition of calmodulin in the presence of Ca2+ (with no added protein kinase) produced a 10-fold increase of phosphorylation involving numerous JTC proteins, including the large (approximately 450,000 Da) ryanodine receptor protein. Calmodulin-dependent phosphorylation of the ryanodine receptor protein was unambiguously demonstrated by Western blot analysis. The specificity of these findings was demonstrated by much lower levels of calmodulin-dependent phosphorylation in light SR as compared to JTC, and by much lower cyclic AMP dependent kinase activity in both JTC and light SR. These observations indicate that the purified JTC contain membrane-bound calmodulin-dependent protein kinase that undergoes autophosphorylation and catalyzes phosphorylation of various membrane proteins. Protein dephosphorylation was very slow in the absence of added phosphatases, but was accelerated by the addition of phosphatase 1 and 2A (catalytic subunit) in the absence of Ca2+, and calcineurin in the presence of Ca2+. Therefore, in the muscle fiber, dephosphorylation of SR proteins relies on cytoplasmic phosphatases. No significant effect of protein phosphorylation was detected on the Ca2(+)-induced Ca2+ release exhibited by isolated JTC vesicles. However, the selective and prominent association of calmodulin-dependent protein kinase and related substrates with junctional membranes, its Ca2+ sensitivity, and its close proximity to the ryanodine and dihydropyridine receptor Ca2+ channels suggest that this phosphorylation system is involved in regulation of functions linked to these structures.