Key result
Endogenous phosphorylation of 160 and 150 kDa sarcoplasmic reticulum proteins is highly dependent on Ca2+ concentration, achieving maximal phosphorylation in less than 15 seconds.
The 160 and 150 kDa proteins of the sarcoplasmic reticulum undergo rapid, Ca2+-dependent endogenous phosphorylation that is distinct from voltage-gated Ca2+ channel subunits.
Ca2+-dependent SR phosphorylation may influence cardiac Ca2+ handling; leaves open protein identities and roles in disease.
The 160 and 150 kDa proteins of sarcoplasmic reticulum (SR) are phosphorylated endogenously. The phosphorylation of both proteins has a marked requirement for Ca2+. Half-maximal and maximal phosphorylation was obtained at about 1 nM- and 1 microM-Ca2+ respectively, and a Hill coefficient of about 0.5 was calculated. The phosphorylation is also dependent on NaF as an inhibitor of the SR phosphoprotein phosphatase. The phosphorylation of these proteins is very rapid, and maximal phosphorylation is achieved in less than 15 s. The phosphorylation of the 160 kDa and 150 kDa polypeptides is completely inhibited by 5 mM-MgCl2 and by 75 microM-LaCl3, by very low concentrations of different detergents, and by preincubation of the SR for 2 min at 60 degrees C. The inhibition by Mg2+ is due to stimulation of ATP hydrolysis, thereby decreasing ATP concentration. Different phosphorylated peptides were obtained by digestion with protease V8 of the 160 kDa and 150 kDa protein bands, suggesting that the 160 kDa and 150 kDa proteins are distinct. The two phosphorylated proteins are present in different fractions and preparations of SR, with or without [3H]PN200-110 binding capacity. These and other results suggest that the phosphorylated SR proteins are distinct from the alpha 1 and alpha 2 subunits of the voltage-gated Ca2+ channel of the T-system membranes. Different inhibitors and activators of protein kinase C and calmodulin-dependent protein kinase have no effect on the endogenous phosphorylation of both polypeptides, suggesting that the phosphorylation is regulated solely by Ca2+. A possible regulatory function for this phosphorylation system is described in the accompanying paper [Gechtman. Orr & Shoshan-Barmatz (1991) Biochem. J. 276.97-102].
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Orr et al. (1991) studied this question. Ca2+ was evaluated on Phosphorylation of 160 and 150 kDa proteins. Endogenous phosphorylation of 160 and 150 kDa sarcoplasmic reticulum proteins is highly dependent on Ca2+ concentration, achieving maximal phosphorylation in less than 15 seconds.
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