Literature DB >> 1098

Studies on an activator of the (Ca2+ plus Mg2+)-ATPase of human erythrocyte membranes.

M G Luthra, G R Hildenbrandt, D J Hanahan.   

Abstract

1. An activator of the (Ca2+ plus Mg2+)-stimulated ATPase present in the human erythrocytes (membrane) has been isolated in soluble form from hemolysates of these cells. Partial purification has been achieved through use of carboxymethyl-Sephadex chromatography. The resulting activator fraction contained no hemoglobin and only 0.3% of the total adenylate kinase activity of the cell. 2. Whereas the activator was released from erythrocytes subjected to hemolysis in 20 miosM buffer at pH 7.6 or at pH 5.8, only the membranes prepared at pH 7.6 were affected by it. 2. Whereas the activator was released from erythrocytes subjected to hemolysis in 20 miosM buffer at pH 7.6 or at pH 5.8, only the membranes prepared at pH 7.6 were affected by it. 3. When (Ca2+ plus Mg2+)-ATPase activity was measured by 32Pi release from (gamma-32P)ATP, freeze-thawed erythrocytes, as well as membranes prepared at pH 5.8 and at pH 7.6, expressed lower values than noted by assay for total Pi release. When ADP instead of ATP was used as substrate, significant amount of Pi were released by these erythrocyte preparations. Further study revealed (a) production of ATP and AMP from ADP with membranes and hemolysate alone, and (b) exchange of the gamma-and B-position phosphate on (gama-32P)ATP in the presence of membranes plus hemolysates. These observations established the presence of adenylate kinase activity in the (membrane-free) hemolysates and in membranes. It further supports the conclusion that Pi release from ADP by human erythrocytes (freeze-thawed) and by their isolated membranes is due to formation of ATP by adenylate kinase and hydrolysis of this generated ATP by (Ca2+ plus Mg2+)-ATPase. 4. The following points were also established: (a) absence of an ADPase in human erythrocytes; (b) the (Ca2+ plus Mg2+)-ATPase activator enhanced cleavage only of the gama-position of ATP and (c) the (Ca2+ plus Mg2+)-ATPase activator is neither adenylate kinase nor hemoglobin.

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Year:  1976        PMID: 1098     DOI: 10.1016/0005-2736(76)90380-1

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  5 in total

1.  Cytochemical approaches to the localization of specific adenosine triphosphatases.

Authors:  J A Firth
Journal:  Histochem J       Date:  1978-05

2.  Reconstitution of the Ca2+-transport system of human erythrocytes.

Authors:  K Gietzen; S Seiler; S Fleischer; H U Wolf
Journal:  Biochem J       Date:  1980-04-15       Impact factor: 3.857

3.  Reversible sodium pump defect and swelling in the diabetic rat erythrocyte: effects on filterability and implications for microangiopathy.

Authors:  R Kowluru; M W Bitensky; A Kowluru; M Dembo; P A Keaton; T Buican
Journal:  Proc Natl Acad Sci U S A       Date:  1989-05       Impact factor: 11.205

4.  A protein activator of Mg2+-dependent, Ca2+-stimulated ATPase in human erythrocyte membranes distinct from calmodulin.

Authors:  D Mauldin; B D Roufogalis
Journal:  Biochem J       Date:  1980-05-01       Impact factor: 3.857

5.  The effect of calmodulin on the phosphoprotein intermediate of Mg2+-dependent Ca2+-stimulated adenosine triphosphatase in human erythrocyte membranes.

Authors:  D A Jeffery; B D Roufogalis; S Katz
Journal:  Biochem J       Date:  1981-02-15       Impact factor: 3.857

  5 in total

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