On the Interrelation between Calmodulin and EGTA in the Regulation of the Affinity to Ca2+ and the Maximal Activity of the Erythrocyte-Membrane Calcium Pump
- 1 May 1983
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 132 (2) , 315-319
- https://doi.org/10.1111/j.1432-1033.1983.tb07364.x
Abstract
Calmodulin distribution in rat erythrocytes and the interrelation between calmodulin and EGTA [ethylene glycol- bis[.beta.-aminoethyl ether]N,N,N''N''-tetraacetic acid] in regulation of the rate of 45Ca accumulation by erythrocyte-membrane inside-out vesicles was studied. The total content of calmodulin in rat erythrocytes is about 24 .mu.mol/l of cells. About 60% of calmodulin is localized in cytoplasm and 40% (10 .mu.mol/l of cells) of calmodulin is loosely bound to membranes; after subsequent washing by hypotonic solution (membranes A) the content of membrane-bound calmodulin decreases up to 0.1 .mu.mol/l of cells. The addition of exogenous calmodulin to membranes A results in increase of the maximal activity of the Ca-pump and does not influence its affinity for Ca2+. Troponin I (30 .mu.M) completely abolishes the calmodulin effect on the Ca-pump activity without significant alterations in its basal activity. The addition of EGTA in the membrane-washing solution results in decrease of the membrane-found pool calmodulin up to 0.01 .mu.mol/l of cells (membranes B). This procedure is accompanied by decrease of the affinity of the Ca-pump for Ca2+ and does not influence its maximal rate. The effect of EGTA treatment (membranes B) on the affinity of Ca-pump to Ca is abolished after addition of micromolar concentrations of calmodulin or millimolar concentration of EGTA in the incubation medium. The increase of EGTA concentration in the incubation medium results in decrease of the affinity of the Ca-pump for calmodulin. Two essentially different pools of calmodulin apparently participate in the regulation of the activity of the Ca-pump. The pool of calmodulin which is loosely bound to membrane (this size is dependent on calmodulin concentration in cytoplasm) determines the maximal activity of the Ca-pump. The effect of this calmodulin pool is blocked by troponin I. The tightly bound pool of calmodulin which is removed by EGTA treatment determines the affinity of the Ca-pump for Ca. In this connection the reasons for contradictory data on estimation of calmodulin effect on the kinetic parameters of the plasma membrane Ca-pump are discussed.This publication has 23 references indexed in Scilit:
- Influence of EGTA on the apparent Ca2+ affinity of Mg2+-dependent, Ca2+-stimulated ATPase in the human erythrocyte membraneBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981
- Active calcium transport in human red cellsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1980
- Calmodulin an activator of human erythrocyte (Ca2+ + Mg2+)-ATPase phosphorylation☆Biochimica et Biophysica Acta (BBA) - General Subjects, 1980
- CalmodulinAnnual Review of Biochemistry, 1980
- Regulation of ATP-dependent Ca-uptake of synaptic plasma membranes by Ca-dependent modulator proteinLife Sciences, 1979
- Enhancement of (Ca2+ + Mg2+)-ATPase activity of human erythrocyte membranes by hemolysis in isosmotic imidazole buffer. II. Dependence on calcium and a cytoplasmic activatorBiochimica et Biophysica Acta (BBA) - Biomembranes, 1977
- Studies on an activator of the (Ca2++Mg2+)-ATPAse of human erythrocyte membranesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976
- Ca2+-stimulated membrane phosphorylation and ATPase activity of the human erythrocyteBiochimica et Biophysica Acta (BBA) - Biomembranes, 1975
- A soluble protein activator of ATPase in human red cell membranesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1973
- Active Calcium Ion Uptake by Inside-Out and Right Side-Out Vesicles of Red Blood Cell MembranesThe Journal of general physiology, 1972