Literature DB >> 2424912

Kell blood group antigens are part of a 93,000-dalton red cell membrane protein.

C M Redman, G Avellino, S R Pfeffer, T K Mukherjee, M Nichols, P Rubinstein, W L Marsh.   

Abstract

Monospecific Kell blood group antibodies, of either human alloimmune or mouse monoclonal origin, react with a single surface-exposed protein of 93,000 daltons. Chymotryptic peptide maps of the 93,000-dalton protein isolated by antibodies of two different specificities (anti-K7 or anti-K14) indicate that Kell epitopes reside on the same protein. Kell protein is similar in size to band 3 protein but differs markedly in its tryptic and chymotryptic peptide maps, indicating that they are different proteins. In addition, sheep antibody to human band 3 does not react with Kell protein. Rabbit antibody to Kell protein reacts, by Western immunoblotting, with membrane proteins from Kell antigen positive red blood cells but not from those of a Ko (Kell null) cell. In intact red cells only a small portion of the Kell protein is available to lactoperoxidase-catalyzed iodination. Under nonreducing conditions Kell antigen is isolated not only as a 93,000-dalton protein but also as larger protein complexes ranging in size from above 200,000 to 115,000 daltons. Treatment of red cells with iodoacetamide, prior to isolation of Kell protein, reduces the amount of the very large complexes, but Kell protein occurs both as 115,000- and 93,000-dalton proteins.

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Year:  1986        PMID: 2424912

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

1.  Molecular cloning and primary structure of Kell blood group protein.

Authors:  S Lee; E D Zambas; W L Marsh; C M Redman
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

2.  Response to erythropoietin in erythroid subclones of the factor-dependent cell line 32D is determined by translocation of the erythropoietin receptor to the cell surface.

Authors:  A R Migliaccio; G Migliaccio; A D'Andrea; M Baiocchi; S Crotta; S Nicolis; S Ottolenghi; J W Adamson
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-15       Impact factor: 11.205

3.  Localization of the McLeod locus (XK) within Xp21 by deletion analysis.

Authors:  C J Bertelson; A O Pogo; A Chaudhuri; W L Marsh; C M Redman; D Banerjee; W A Symmans; T Simon; D Frey; L M Kunkel
Journal:  Am J Hum Genet       Date:  1988-05       Impact factor: 11.025

4.  Regional chromosomal assignment of the Kell blood group locus (KEL) to chromosome 7q33-q35 by fluorescence in situ hybridization: evidence for the polypeptide nature of antigenic variation.

Authors:  M T Murphy; N Morrison; J S Miles; R H Fraser; N K Spurr; E Boyd
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

5.  An easy and efficient strategy for KEL genotyping in a multiethnic population.

Authors:  Carine Prisco Arnoni; Janaína Guinhem Muniz; Tatiane Aparecida de Paula; Rosangela Duarte de Medeiros Person; Diana Gazito; Wilson Baleotti; José Augusto Barreto; Lilian Castilho; Flavia Roche Moreira Latini
Journal:  Rev Bras Hematol Hemoter       Date:  2013

6.  Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

Authors:  M F Ho; A P Monaco; L A Blonden; G J van Ommen; N A Affara; M A Ferguson-Smith; H Lehrach
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

7.  In vitro evaluation of the role of the Duffy blood group in erythrocyte invasion by Plasmodium vivax.

Authors:  J W Barnwell; M E Nichols; P Rubinstein
Journal:  J Exp Med       Date:  1989-05-01       Impact factor: 14.307

8.  Clinical and molecular research of neuroacanthocytosis.

Authors:  Lihong Zhang; Suping Wang; Jianwen Lin
Journal:  Neural Regen Res       Date:  2013-03-25       Impact factor: 5.135

Review 9.  A Comprehensive Review of Our Current Understanding of Red Blood Cell (RBC) Glycoproteins.

Authors:  Takahiko Aoki
Journal:  Membranes (Basel)       Date:  2017-09-29
  9 in total

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