Caclium uptake and associated adenosine triphosphatase activity in fragmented sarcoplasmic reticulum. Requirement for potassium ions
- PMID: 14156
Caclium uptake and associated adenosine triphosphatase activity in fragmented sarcoplasmic reticulum. Requirement for potassium ions
Abstract
The effects of monovalent cations on calcium uptake by fragmented sarcoplasmic reticulum have been clarified. Homogenization of muscle tissue in salt-containing solutions leads to contamination of this subcellular fraction with actomyosin and mitochondrial membranes. When, in addition, inorganic cations are contributed by the microsomal suspension and in association with nucleotide triphosphate substrates there is an apparent inhibition of the calcium transport system by potassium and other cations. However, when purified preparations were obtained after homogenization in sucrose medium followed by centrifugation on a sucrose density gradient in a zonal rotor, calcium uptake and the associated adenosine triphosphatase activity were considerably activated by potassium and other univalent cations. When plotted against the log of the free calcium concentration there was only a slight increase in calcium uptake and ATPase activity in the absence of potassium ions but sigmoid-shaped curves were obtained in 100 mM K+ with half-maximal stimulation occurring at 2 muM Ca2+ for both calcium uptake and ATPase activity. The augmentation in calcium uptake was not due to an ionic strength effect as Tris cation at pH 6.6 was shown to be inactive in this respect. Other monovalent cations were effective in the order K+ greater than Na+ greater than NH4+=Rb+=Cs+ greater than Li+ with half-maximal stimulation in 11 mM K+, 16 mM Na+, 25 mM NH4+, Rb+, and Cs+ and in 50 mM Li+. There was nos synergistic action between K+ AND Na+ ions and both calcium uptak and associated ATPase were insensitive to ouabain. Thallous ions stimulate many K+-requiring enzymes and at one-tenth the concentration were nearly as effective as K+ ions in promoting calcium uptake. The ratio of Ca2+ ions transported to P1 released remained unchanged at 2 after addition of K+ ions indicating an effect on the rate of calcium uptake rather than an increased efficiency of uptake. In support of this it was found that during the stimulation of calcium uptake by Na+ ions there was a reduction in the steady state concentration of phosphorylated intermediate formed from [gamma-32P]ATP. It is considered that there is a physiological requirement for potassium ions in the relaxation process.
Similar articles
-
Activation of calcium transport in skeletal muscle sarcoplasmic reticulum by monovalent cations.J Biol Chem. 1976 Nov 25;251(22):6947-52. J Biol Chem. 1976. PMID: 136443
-
Proton inactivation of Ca2+ transport by sarcoplasmic reticulum.J Biol Chem. 1977 Feb 10;252(3):994-1001. J Biol Chem. 1977. PMID: 14142
-
Calcium transport ATPase of canine cardiac sarcoplasmic reticulum. A comparison with that of rabbit fast skeletal muscle sarcoplasmic reticulum.J Biol Chem. 1976 Nov 25;251(22):6894-900. J Biol Chem. 1976. PMID: 11210
-
Purification (Na+ plus K+)-ATPase: active site determinations and criteria of purity.Ann N Y Acad Sci. 1974;242(0):36-52. doi: 10.1111/j.1749-6632.1974.tb19077.x. Ann N Y Acad Sci. 1974. PMID: 4279596 Review. No abstract available.
-
Sodium Ions as Regulators of Transcription in Mammalian Cells.Biochemistry (Mosc). 2022 Aug;87(8):789-799. doi: 10.1134/S0006297922080107. Biochemistry (Mosc). 2022. PMID: 36171659 Review.
Cited by
-
Effects of sodium gradient manipulation upon cellular calcium, 45Ca fluxes and cellular sodium in the guinea-pig taenia coli.J Physiol. 1981;319:443-61. doi: 10.1113/jphysiol.1981.sp013920. J Physiol. 1981. PMID: 7320922 Free PMC article.
-
Effect of K+, and other ligands on the thiol reactivity and tryptic cleavage pattern of scallop sarcoplasmic reticulum.J Muscle Res Cell Motil. 1989 Jun;10(3):229-44. doi: 10.1007/BF01739813. J Muscle Res Cell Motil. 1989. PMID: 2527247
-
Thermodynamic and kinetic cooperativity in ligand binding to multiple sites on a protein: Ca2+ activation of an ATP-driven Ca pump.Proc Natl Acad Sci U S A. 1985 Jul;82(14):4688-92. doi: 10.1073/pnas.82.14.4688. Proc Natl Acad Sci U S A. 1985. PMID: 3161074 Free PMC article.
-
Interactions of physiological ligands with the Ca pump and Na/Ca exchange in squid axons.J Gen Physiol. 1984 Dec;84(6):895-914. doi: 10.1085/jgp.84.6.895. J Gen Physiol. 1984. PMID: 6097638 Free PMC article.
-
Arsenazo III and antipyrylazo III calcium transients in single skeletal muscle fibers.J Gen Physiol. 1982 Apr;79(4):679-707. doi: 10.1085/jgp.79.4.679. J Gen Physiol. 1982. PMID: 6802933 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous