Literature DB >> 14156

Caclium uptake and associated adenosine triphosphatase activity in fragmented sarcoplasmic reticulum. Requirement for potassium ions.

P F Duggan.   

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.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 14156

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  14 in total

1.  Thermodynamic and kinetic cooperativity in ligand binding to multiple sites on a protein: Ca2+ activation of an ATP-driven Ca pump.

Authors:  C Tanford; J A Reynolds; E A Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

2.  Modulation of stoichiometry of the sarcoplasmic reticulum calcium pump may enhance thermodynamic efficiency.

Authors:  A Gafni; P D Boyer
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

3.  Effects of Na readmission on cellular 45Ca fluxes in Na-depleted guinea pig taenia coli.

Authors:  P Aaronson; C Van Breemen
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

Review 4.  Monovalent ion and calcium ion fluxes in sarcoplasmic reticulum.

Authors:  G Meissner
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

5.  Rapid kinetic studies of active Ca2+ transport in sarcoplasmic reticulum.

Authors:  V C Chiu; D H Haynes
Journal:  J Membr Biol       Date:  1980-10-31       Impact factor: 1.843

6.  Inhibition of SERCA2 Ca(2+)-ATPases by Cs(+).

Authors:  Gary J Kargacin; Roozbeh Aschar-Sobbi; Margaret E Kargacin
Journal:  Pflugers Arch       Date:  2004-10-12       Impact factor: 3.657

7.  Effects of sodium gradient manipulation upon cellular calcium, 45Ca fluxes and cellular sodium in the guinea-pig taenia coli.

Authors:  P Aaronson; C van Breemen
Journal:  J Physiol       Date:  1981       Impact factor: 5.182

8.  Effects of K+ on the binding of Ca2+ to the Ca(2+)-ATPase of sarcoplasmic reticulum.

Authors:  A G Lee; K Baker; Y M Khan; J M East
Journal:  Biochem J       Date:  1995-01-01       Impact factor: 3.857

9.  Effects of Mg2+, anions and cations on the Ca2+ + Mg2+-activated ATPase of sarcoplasmic reticulum.

Authors:  H I Stefanova; R M Napier; J M East; A G Lee
Journal:  Biochem J       Date:  1987-08-01       Impact factor: 3.857

10.  Arsenazo III and antipyrylazo III calcium transients in single skeletal muscle fibers.

Authors:  P Palade; J Vergara
Journal:  J Gen Physiol       Date:  1982-04       Impact factor: 4.086

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.