Literature DB >> 7441724

Ion movement accompanied by calcium uptake of sarcoplasmic reticulum vesicles studied through the osmotic volume change by the light scattering method.

T Kometani, M Kasai.   

Abstract

The volume change of sarcoplasmic reticulum vesicles was induced by Ca2+ uptake. This volume change was measured by the light-scattering method. When vesicles were shrunk beforehand under the condition that anions are more permeable than cations, they swelled during Ca2+ uptake due to the concomitant incorporation of anions. On the contrary, they shrank with Ca2+ uptake due to the extrusion of cations under the condition that cations are more permeable than anions. From the analysis of the volume change it was concluded that all ions other than Ca2+ were transported passively in order to neutralize the membrane potential generated by the Ca2+ pump. These results support the idea that the Ca2+ pump is electrogenic. By using this technique, it became possible to measure the fast Ca2+ uptake rate. The dependence of the Ca2+ uptake rate on the Ca2+ concentration suggests that the site at which Ca2+ inhibits Ca2+ uptake is located inside the vesicle. From the osmotic response of the vesicles, the intravesicular concentration of free Ca2+ was estimated to be about 15 mM, when Ca2+ was fully taken up under the physiological condition.

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Year:  1980        PMID: 7441724     DOI: 10.1007/bf01875967

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  18 in total

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Authors:  D H MacLennan; P C Holland
Journal:  Annu Rev Biophys Bioeng       Date:  1975

2.  [ON THE MECHANISM OF CALCIUM TRANSPORT ACROSS THE MEMBRANE OF THE SARCOPLASMIC RETICULUM].

Authors:  W HASSELBACH; M MAKINOSE
Journal:  Biochem Z       Date:  1963-10-14

3.  The structure of the calcium complex of A23187, a divalent cation ionophore antibiotic.

Authors:  M O Chaney; N D Jones; M Debono
Journal:  J Antibiot (Tokyo)       Date:  1976-04       Impact factor: 2.649

4.  Depolarization-induced calcium release from sarcoplasmic reticulum fragments. I. Release of calcium taken up upon using ATP.

Authors:  M Kasai; H Miyamoto
Journal:  J Biochem       Date:  1976-05       Impact factor: 3.387

5.  Elementary processes in the hydrolysis of ATP by sarcoplasmic reticulum membranes.

Authors:  A Martonosi; E Lagwinska; M Oliver
Journal:  Ann N Y Acad Sci       Date:  1974-02-18       Impact factor: 5.691

6.  Determination of reflection coefficients for various ions and neutral molecules in sarcoplasmic reticulum vesicles through osmotic volume change studied by stopped flow technique.

Authors:  M Kasai; T Kanemasa; S Fukumoto
Journal:  J Membr Biol       Date:  1979-12-31       Impact factor: 1.843

7.  Ionic permeability of sarcoplasmic reticulum vesicles measured by light scattering method.

Authors:  T Kometani; M Kasai
Journal:  J Membr Biol       Date:  1978-07-18       Impact factor: 1.843

8.  Asymmetric distribution of calcium binding sites of sarcoplasmic reticulum fragments.

Authors:  H Miyamoto; M Kasai
Journal:  J Biochem       Date:  1979-03       Impact factor: 3.387

9.  A relation between calcium binding and turbidity change in isolated sarcoplasmic reticulum.

Authors:  T Onishi; T Terasaki
Journal:  J Biochem       Date:  1967-06       Impact factor: 3.387

10.  Sarcoplasmic reticulum. IX. The permeability of sarcoplasmic reticulum membranes.

Authors:  P F Duggan; A Martonosi
Journal:  J Gen Physiol       Date:  1970-08       Impact factor: 4.086

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  3 in total

1.  Osmotic changes of sarcoplasmic reticulum vesicles during Ca2+ uptake.

Authors:  T Beeler
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

2.  Is the red cell calcium pump electrogenic?

Authors:  J P Rossi; H J Schatzmann
Journal:  J Physiol       Date:  1982-06       Impact factor: 5.182

3.  Single channel characteristics of a high conductance anion channel in "sarcoballs".

Authors:  G D Hals; P G Stein; P T Palade
Journal:  J Gen Physiol       Date:  1989-03       Impact factor: 4.086

  3 in total

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