Literature DB >> 830369

Increased membrane binding of erythrocyte catalase in hereditary spherocytosis and in metabolically stressed normal cells.

D W Allen, S Cadman, S R McCann, B Finkel.   

Abstract

Normal red blood cell (RBC) membranes were compared with (1) RBC membranes from six patients with hereditary spherocytosis (HS), (2) normal membranes after hemolysis of the RBC in the presence of calcium, or (3) normal membranes after incubation of RBC for 24 hr in phosphate-buffered saline containing calcium without added glucose. When compared with normal controls, polyacrylamide gel electrophoresis with sodium dodecyl sulfate (PAGE SDS) of all three preparations showed an increase in membrane binding of globin and protein band 4.5 (60,000 molecular weight). In an attempt to identify band 4.5, 14 enzymes were assayed in the RBC membranes. Of these, catalase and lactate dehydrogenase were increased in membranes from HS RBC and from normal cells exposed to calcium. Only catalase, however, was present in sufficient quantity and had the correct subunit molecular weight on PAGE SDS and calcium-dependent membrane binding to account for an appreciable portion of 4.5. Caralase was further identified with a component of band 4.5 by double immunodiffusion using a specific anti-catalase antibody.

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Year:  1977        PMID: 830369

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  11 in total

1.  Diminished spectrin extraction from ATP-depleted human erythrocytes. Evidence relating spectrin to changes in erythrocyte shape and deformability.

Authors:  S E Lux; K M John; T E Ukena
Journal:  J Clin Invest       Date:  1978-03       Impact factor: 14.808

2.  Molecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesicles.

Authors:  O S Platt; J F Falcone; S E Lux
Journal:  J Clin Invest       Date:  1985-01       Impact factor: 14.808

3.  Membrane protein lesions in erythrocytes with Heinz bodies.

Authors:  O S Platt; J F Falcone
Journal:  J Clin Invest       Date:  1988-09       Impact factor: 14.808

4.  Molecular defect in the membrane skeleton of blood bank-stored red cells. Abnormal spectrin-protein 4.1-actin complex formation.

Authors:  L C Wolfe; A M Byrne; S E Lux
Journal:  J Clin Invest       Date:  1986-12       Impact factor: 14.808

5.  The isolation and characterization of 60 nm vesicles ('nanovesicles') produced during ionophore A23187-induced budding of human erythrocytes.

Authors:  D Allan; P Thomas; A R Limbrick
Journal:  Biochem J       Date:  1980-06-15       Impact factor: 3.857

6.  Gel electrophoresis of the human erythrocyte membrane proteins: aberrant patterns in hematological and non-hematological diseases.

Authors:  V Anselstetter
Journal:  Blut       Date:  1978-03-15

7.  On the interactions of catalase with subcellular structure.

Authors:  M Pegg; D Crane; C Masters
Journal:  Mol Cell Biochem       Date:  1989-03-16       Impact factor: 3.396

8.  Decreased survival in vivo of diamide-incubated dog erythrocytes. A model of oxidant-induced hemolysis.

Authors:  G J Johnson; D W Allen; T P Flynn; B Finkel; J G White
Journal:  J Clin Invest       Date:  1980-11       Impact factor: 14.808

9.  Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.

Authors:  E Shinar; E A Rachmilewitz; S E Lux
Journal:  J Clin Invest       Date:  1989-02       Impact factor: 14.808

Review 10.  Acatalasemia.

Authors:  M Ogata
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

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