Literature DB >> 6721859

Nonidet P-40 extraction of lymphocyte plasma membrane. Characterization of the insoluble residue.

A A Davies, N M Wigglesworth, D Allan, R J Owens, M J Crumpton.   

Abstract

Purified preparations of lymphocyte plasma membrane were extracted exhaustively with Nonidet P-40 in Dulbecco's phosphate-buffered saline medium. The insoluble fraction, as defined by sedimentation at 10(6) g-min, contained about 10% of the membrane protein as well as cholesterol and phospholipid. The lipid/protein ratio, cholesterol/phospholipid ratio and sphingomyelin content were increased in the residue. Density-gradient centrifugation suggested that the lipid and protein form a common entity. As judged by sodium dodecyl sulphate/polyacrylamide-gel electrophoresis, the Nonidet P-40-insoluble fractions of the plasma membranes of human B lymphoblastoid cells and pig mesenteric lymph-node lymphocytes possessed similar qualitative polypeptide compositions but differed quantitatively. Both residues comprised major polypeptides of Mr 28 000, 33 000, 45 000 and 68 000, together with a prominent band of Mr 120 000 in the human and of Mr 200 000 in the pig. The polypeptides of Mr 28 000, 33 000, 68 000 and 120 000 were probably located exclusively in the Nonidet P-40-insoluble residue, which also possessed a 4-fold increase in 5'-nucleotidase specific activity. The results indicate that a reproducible fraction of lymphocyte plasma membrane is insoluble in non-ionic detergents and that this fraction possesses a unique polypeptide composition. By analogy with similar studies with erythrocyte ghosts, it appears likely that the polypeptides are located on the plasma membrane's cytoplasmic face.

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Year:  1984        PMID: 6721859      PMCID: PMC1153477          DOI: 10.1042/bj2190301

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  28 in total

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3.  Actin associated with purified lymphocyte plasma membrane.

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4.  Transmembrane interactions and the mechanism of capping of surface receptors by their specific ligands.

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Review 5.  Preparation and properties of lymphocyte plasma membrane.

Authors:  M J Crumpton; D Snary
Journal:  Contemp Top Mol Immunol       Date:  1974

6.  Preparation and characterization of the plasma membrane of pig lymphocytes.

Authors:  D Allan; M J Crumpton
Journal:  Biochem J       Date:  1970-11       Impact factor: 3.857

7.  The site of diphosphoinositide synthesis in rat liver.

Authors:  R H Michell; J N Hawthorne
Journal:  Biochem Biophys Res Commun       Date:  1965-11-22       Impact factor: 3.575

8.  Selective solubilization of proteins and phospholipids from red blood cell membranes by nonionic detergents.

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Review 9.  Surface modulation in cell recognition and cell growth.

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Journal:  Science       Date:  1976-04-16       Impact factor: 47.728

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  11 in total

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Authors:  R Kobayashi; Y Tashima
Journal:  Biochem J       Date:  1989-09-15       Impact factor: 3.857

2.  Isolation and characterization of a novel 68,000-Mr Ca2+-binding protein of lymphocyte plasma membrane.

Authors:  R J Owens; M J Crumpton
Journal:  Biochem J       Date:  1984-04-01       Impact factor: 3.857

3.  Characterization of a cytoskeletal matrix associated with myelin from rat brain.

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Authors:  A A Davies; S E Moss; M R Crompton; T A Jones; N K Spurr; D Sheer; C Kozak; M J Crumpton
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

7.  Primary structure of the human, membrane-associated Ca2+-binding protein p68 a novel member of a protein family.

Authors:  M R Crompton; R J Owens; N F Totty; S E Moss; M D Waterfield; M J Crumpton
Journal:  EMBO J       Date:  1988-01       Impact factor: 11.598

8.  Cellular distribution of p68, a new calcium-binding protein from lymphocytes.

Authors:  R J Owens; C J Gallagher; M J Crumpton
Journal:  EMBO J       Date:  1984-05       Impact factor: 11.598

9.  Agorins: major structural proteins of the plasma membrane skeleton of P815 tumor cells.

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10.  Triton X-100 extraction of P815 tumor cells: evidence for a plasma membrane skeleton structure.

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