Literature DB >> 2524225

Effect of Mg2+ concentration on Ca2+ uptake kinetics and structure of the sarcoplasmic reticulum membrane.

F J Asturias1, J K Blasie.   

Abstract

Direct measurements of phosphorylation of the Ca2+ ATPase of the sarcoplasmic reticulum (SR) have shown that the lifetime of the first phosphorylated intermediate in the Ca2+ transport cycle, E1 approximately P, increases with decreasing [Mg2+] (Dupont, Y. 1980. Eur. J. Biochem. 109:231-238). Previous x-ray diffraction work (Pascolini, D., and J.K. Blasie. 1988. Biophys. J. 54:669-678) under high [Mg2+] conditions (25 mM) indicated that changes in the profile structure of the SR membrane could be responsible for the low-temperature transient trapping of E1 approximately P that occurs at temperatures below 2-3 degrees C, the upper characteristic temperature th for lipid lateral phase separation in the membrane. We now present results of our study of the Ca2+ uptake kinetics and of the structure of the SR membrane at low [Mg2+] (less than or equal to 100 microM). Our results show a slowing in the kinetics of both phases of the Ca2+ uptake process and an increase in the duration of the plateau of the fast phase before the onset of the slow phase, indicating an increase in the lifetime (transient trapping) of E1 approximately P. Calcium uptake kinetics at low [Mg2+] and moderately low temperature (approximately 0 degree C) are similar to those observed at much lower temperatures (approximately -10 degrees C) at high [Mg2+]. The temperature-induced structural changes that we observed at low [Mg2+] are much more pronounced than those found to occur at higher [Mg2+]. Also, at the lower [Mg2+] the upper characteristic temperature th for lipid lateral phase separation was found to be higher, at approximately 8-10 degrees C. Our studies indicate that both temperature and [Mg2+] affect the structure and the functionality (as measured by changes in the kinetics of Ca2+ uptake) of the SR membrane. Membrane lipid phase behavior and changes in the Ca2+ ATPase profile structure seem to be related, and we have found that structural changes are responsible for the slowing of the kinetics of the fast phase of Ca2+ uptake, and could also mediate the effect that [Mg2+] has on E1 approximately P lifetime.

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Year:  1989        PMID: 2524225      PMCID: PMC1330558          DOI: 10.1016/S0006-3495(89)82873-5

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  28 in total

Review 1.  Energy interconversion by the Ca2+-dependent ATPase of the sarcoplasmic reticulum.

Authors:  L de Meis; A L Vianna
Journal:  Annu Rev Biochem       Date:  1979       Impact factor: 23.643

2.  Slow transition of phosphoenzyme from ADP-sensitive to ADP-insensitive forms in solubilized Ca2+, Mg2+-ATPase of sarcoplasmic reticulum: evidence for retarded dissociation of Ca2+ from the phosphoenzyme.

Authors:  Y Takakuwa; T Kanazawa
Journal:  Biochem Biophys Res Commun       Date:  1979-06-27       Impact factor: 3.575

3.  A direct analysis of lamellar x-ray diffraction from hydrated oriented multilayers of fully functional sarcoplasmic reticulum.

Authors:  L Herbette; J Marquardt; A Scarpa; J K Blasie
Journal:  Biophys J       Date:  1977-11       Impact factor: 4.033

4.  Comparative studies on the effects of pH and Ca2+ on bilayers of various negatively charged phospholipids and their mixtures with phosphatidylcholine.

Authors:  P W van Dijck; B de Kruijff; A J Verkleij; L L van Deenen; J de Gier
Journal:  Biochim Biophys Acta       Date:  1978-09-11

5.  Structure determination of asymmetric membrane profiles using an iterative Fourier method.

Authors:  R M Stroud; D A Agard
Journal:  Biophys J       Date:  1979-03       Impact factor: 4.033

6.  Occlusion of divalent cations in the phosphorylated calcium pump of sarcoplasmic reticulum.

Authors:  Y Dupont
Journal:  Eur J Biochem       Date:  1980-08

7.  Kinetics of calcium uptake by isolated sarcoplasmic reticulum vesicles using flash photolysis of caged adenosine 5'-triphosphate.

Authors:  D H Pierce; A Scarpa; M R Topp; J K Blasie
Journal:  Biochemistry       Date:  1983-11-08       Impact factor: 3.162

8.  Reaction mechanism of Ca2+-dependent adenosine triphosphatase of sarcoplasmic reticulum. ATP hydrolysis with CaATP as a substrate and role of divalent cation.

Authors:  M Shigekawa; S Wakabayashi; H Nakamura
Journal:  J Biol Chem       Date:  1983-07-25       Impact factor: 5.157

9.  Effect of divalent cation bound to the ATPase of sarcoplasmic reticulum. Activation of phosphoenzyme hydrolysis by Mg2+.

Authors:  M Shigekawa; S Wakabayashi; H Nakamura
Journal:  J Biol Chem       Date:  1983-12-10       Impact factor: 5.157

10.  X-ray diffraction and electron microscope study of phase separation in rod outer segment photoreceptor membrane multilayers.

Authors:  S M Gruner; K J Rothschild; N A Clark
Journal:  Biophys J       Date:  1982-09       Impact factor: 4.033

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  7 in total

1.  Location of high-affinity metal binding sites in the profile structure of the Ca+2-ATPase in the sarcoplasmic reticulum by resonance x-ray diffraction.

Authors:  F J Asturias; J K Blasie
Journal:  Biophys J       Date:  1991-02       Impact factor: 4.033

2.  Large-scale structural changes in the sarcoplasmic reticulum ATPase appear essential for calcium transport.

Authors:  J K Blasie; D Pascolini; F Asturias; L G Herbette; D Pierce; A Scarpa
Journal:  Biophys J       Date:  1990-09       Impact factor: 4.033

Review 3.  Lipids and the ocular lens.

Authors:  Douglas Borchman; Marta C Yappert
Journal:  J Lipid Res       Date:  2010-04-20       Impact factor: 5.922

4.  Entropic drive in the sarcoplasmic reticulum ATPase interaction with Mg2+ and Pi.

Authors:  F P Schwarz; G Inesi
Journal:  Biophys J       Date:  1997-10       Impact factor: 4.033

5.  Evidence that lipid lateral phase separation induces functionally significant structural changes in the Ca+2ATPase of the sarcoplasmic reticulum.

Authors:  F J Asturias; D Pascolini; J K Blasie
Journal:  Biophys J       Date:  1990-07       Impact factor: 4.033

6.  Effect of Ca2+ binding on the profile structure of the sarcoplasmic reticulum membrane using time-resolved x-ray diffraction.

Authors:  L J DeLong; J K Blasie
Journal:  Biophys J       Date:  1993-06       Impact factor: 4.033

7.  Changes in the profile structure of the sarcoplasmic reticulum membrane induced by phosphorylation of the Ca2+ ATPase enzyme in the presence of terbium: a time-resolved x-ray diffraction study.

Authors:  F J Asturias; R F Fischetti; J K Blasie
Journal:  Biophys J       Date:  1994-05       Impact factor: 4.033

  7 in total

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