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PMID: 1098 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Biochimica et biophysica acta ·Vol. 419 ·No. 1 ·1976-01-08 ·Pages 164-79

Luthra MG, Hildenbrandt GR, Hanahan DJ

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.

MeSH Terms
Adenosine Triphosphatases/metabolism Blood Proteins/physiology Calcium/pharmacology Cell Fractionation Cell Membrane/drug effects,enzymology Enzyme Activation/drug effects Erythrocytes/drug effects,enzymology Humans Hydrogen-Ion Concentration Kinetics Magnesium/pharmacology
Chemicals
Blood Proteins Adenosine Triphosphatases Magnesium Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Luthra M G
Hildenbrandt G R
Hanahan D J
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1976-01-08
Pages
164-79
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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