Answers are grounded in this paper and cite their sources.
Actin-activated ATP hydrolysis by phosphorylated arterial myosin is Ca2+-dependent at Mg2+ concentrations which allow myosin to bind 2 mol of Ca2+ per mol (S. Chacko and A. Rosenfeld (1982) Proc. Natl. Acad. Sci. U. S. A. 79, 292-296). The possible effects of myosin filament formation and conformational change involving the rod portion of the myosin molecule on actin-myosin interaction and actin-activated ATP hydrolysis was eliminated by utilizing soluble heavy meromyosin (HMM). HMM was prepared from phosphorylated arterial myosin by chymotryptic digestion and purified by gel filtration on Sepharose CL-6B. Actin-activated ATPase activity of the phosphorylated HMM was measured either at constant Mg2+ and variable Ca2+ or at constant Ca2+ and variable Mg2+ concentrations. At constant (0.05 M) ionic strength and pCa 5, the actin-activated ATPase activity increased until the free Mg2+ reached between 0.5-1 mM; this was followed by a decrease in activity to a very low level at 7 mM free Mg2+. Removal of Ca2+ at 1 mM free Mg2+ lowered the actin-activated ATPase activity (40-60% inhibition). These experiments demonstrated that Mg2+ and Ca2+ had a direct effect on actin-activated ATP hydrolysis. This effect was not due to myosin filament formation and was independent of the conformational change involving the rod portion of the myosin molecule.
No takes yet. Share an insight, caveat, or question.
Kaminski et al. (1984) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: