The effect of monovalent and divalent cations on the ATP-dependent Ca2+-binding and phosphorylation during the reaction cycle of the sarcoplasmic reticulum Ca2+-transport ATPase
- PMID: 2954819
- DOI: 10.1111/j.1432-1033.1987.tb11435.x
The effect of monovalent and divalent cations on the ATP-dependent Ca2+-binding and phosphorylation during the reaction cycle of the sarcoplasmic reticulum Ca2+-transport ATPase
Abstract
The coupling of Ca2+ movements and phosphate fluxes as well as the time-dependent occurrence of sequential reaction intermediates in the forward mode of the Ca,Mg-dependent ATPase reaction have been investigated using leaky vesicles (A23187) in the presence of varying Ca2+, Mg2+, and K+ concentrations. The employed ATP concentration of 2 microM does not allow more than one reaction cycle to occur. The respective fractions of ADP-sensitive and ADP-insensitive phosphoenzyme have been determined. The chosen experimental conditions (0-1 degree C, pH 6.0, absence of solubilizers) allow a prolonged time of observation and exclude interfering alterations of coupling and binding parameters, respectively. It is shown that under the experimental conditions K+ interacts with at least four different reaction steps (phosphoenzyme formation, E1P----E2P transition, E2P hydrolysis, and E2----E1 transformation). Mg2+ represents the sole ionic co-factor for the formation of the substrate MgATP if it is present in high concentrations (5 mM). Additional Ca2+ is bound to the substrate as well as to unspecific sites otherwise occupied by Mg2+ if Mg2+ is reduced to 0.1 mM. In this case the E1P----E2P transition rate (including Ca2+ translocation and Ca2+ release from low-affinity sites) is little diminished. If, in the absence of K+, both Mg2+ and Ca2+ are deficient E2P hydrolysis is vastly retarded. We find Ca2+ release to occur time-coincidently with E1P formation and not concomitantly with the comparably slow appearance of E2P; the molar amount of Ca2+ released, however, rather agreed with that of E2P formed. This suggests that under the prevailing conditions of a high proton concentration, phosphoenzyme states containing occluded Ca2+ or Ca2+ bound to low-affinity sites are transitional and not detectable. Preliminary findings on this subject have been published by us and colleagues from this laboratory [Hasselbach, W., Agostini, B., Medda, P., Migala, A. & Waas, W. (1985) in The sarcoplasmic reticulum calcium pump: Early and recent developments critically overviewed (Fleischer, S. & Tonomura, Y., eds) pp. 19-49, Academic Press, Orlando].
Similar articles
-
Effect of metal bound to the substrate site on calcium release from the phosphoenzyme intermediate of sarcoplasmic reticulum ATPase.J Biol Chem. 1987 Aug 25;262(24):11524-31. J Biol Chem. 1987. PMID: 2957367
-
Reaction mechanism of Ca2+-dependent adenosine triphosphatase of sarcoplasmic reticulum. ATP hydrolysis with CaATP as a substrate and role of divalent cation.J Biol Chem. 1983 Jul 25;258(14):8698-707. J Biol Chem. 1983. PMID: 6223035
-
The time-dependent distribution of phosphorylated intermediates in native sarcoplasmic reticulum Ca2+-ATPase from skeletal muscle is not compatible with a linear kinetic model.Biochemistry. 2004 Apr 13;43(14):4400-16. doi: 10.1021/bi035068g. Biochemistry. 2004. PMID: 15065885
-
Coupling of hydrolysis of ATP and the transport of Ca2+ by the calcium ATPase of sarcoplasmic reticulum.Biochem Soc Trans. 1992 Aug;20(3):555-9. doi: 10.1042/bst0200555. Biochem Soc Trans. 1992. PMID: 1426591 Review. No abstract available.
-
Charge changes in sarcoplasmic reticulum and Ca2+-ATPase induced by calcium binding and release: a study using lipophilic ions.Membr Biochem. 1986;6(4):291-307. doi: 10.3109/09687688609065454. Membr Biochem. 1986. PMID: 2952866 Review.
Cited by
-
Modulation of P2X4 pore closure by magnesium, potassium, and ATP.Biophys J. 2022 Apr 5;121(7):1134-1142. doi: 10.1016/j.bpj.2022.02.038. Epub 2022 Mar 3. Biophys J. 2022. PMID: 35248546 Free PMC article.
-
Effects of K+ on the binding of Ca2+ to the Ca(2+)-ATPase of sarcoplasmic reticulum.Biochem J. 1995 Jan 1;305 ( Pt 1)(Pt 1):225-31. doi: 10.1042/bj3050225. Biochem J. 1995. PMID: 7826333 Free PMC article.
-
Ca2+ release to lumen from ADP-sensitive phosphoenzyme E1PCa2 without bound K+ of sarcoplasmic reticulum Ca2+-ATPase.J Biol Chem. 2010 Dec 3;285(49):38674-83. doi: 10.1074/jbc.M110.183343. Epub 2010 Oct 11. J Biol Chem. 2010. PMID: 20937807 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
-
Pre-steady-state kinetic study of the effects of K+ on the partial reactions of the catalytic cycle of the plasma membrane Ca(2+)-ATPase.Biochem J. 1996 Apr 15;315 ( Pt 2)(Pt 2):673-7. doi: 10.1042/bj3150673. Biochem J. 1996. PMID: 8615846 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous