Literature DB >> 3345289

Biochemical studies on McLeod phenotype red cells and isolation of Kx antigen.

C M Redman1, W L Marsh, A Scarborough, C L Johnson, B I Rabin, M Overbeeke.   

Abstract

Red cells of the McLeod blood group phenotype have weak Kell antigens, lack Kx antigen and have acanthocytic morphology. We have immunoprecipitated Kell antigens from McLeod red cells and show that they are markers on the same 93 kDa membrane protein that carries Kell antigens on normal red cells. However, as determined by Western immunoblotting, McLeod red cells have a marked deficiency of this protein. We have also studied the near-neighbour relationship of McLeod and common Kell red-cell membrane proteins by cross-linking intrinsic sulphydryl groups by oxidation, catalysed with orthophenanthroline and copper, or by cross-linking amino groups with dimethyl-3,3'-dithiobispropionimidate. Results were analysed by diagonal mapping in two-dimensional gels. No abnormalities of membrane protein inter-relationship were detected in McLeod red cells. We have isolated Kx antigen from K0 red cells by immunoprecipitation with human alloimmune anti-Kx serum, isolation of immune complexes from detergent-solubilized cell membranes with protein A-Sepharose and analysis of the eluted immune complex by SDS-PAGE under reducing conditions. Kx antigen is a marker on a red-cell membrane protein of approximately 37 kDa. Ko (Knull) red cells have about twice the amount of Kx antigen as do red cells of common Kell type. McLeod red cells have no detectable Kx antigen by serological tests or by immunoprecipitation.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3345289     DOI: 10.1111/j.1365-2141.1988.tb04191.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  8 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.  Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).

Authors:  N D Carter; J E Morgan; A P Monaco; M S Schwartz; S Jeffery
Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318

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.  Shape determinants of McLeod acanthocytes.

Authors:  J K Khodadad; R S Weinstein; L W Marsh; T L Steck
Journal:  J Membr Biol       Date:  1989-03       Impact factor: 1.843

5.  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

Review 6.  McLeod syndrome: a distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations.

Authors:  T N Witt; A Danek; M Reiter; M U Heim; J Dirschinger; E G Olsen
Journal:  J Neurol       Date:  1992-07       Impact factor: 4.849

Review 7.  Biological roles of blood group antigens.

Authors:  W L Marsh
Journal:  Yale J Biol Med       Date:  1990 Sep-Oct

8.  A partnership between the lipid scramblase XK and the lipid transfer protein VPS13A at the plasma membrane.

Authors:  Andrés Guillén-Samander; Yumei Wu; S Sebastian Pineda; Francisco J García; Julia N Eisen; Marianna Leonzino; Berrak Ugur; Manolis Kellis; Myriam Heiman; Pietro De Camilli
Journal:  Proc Natl Acad Sci U S A       Date:  2022-08-22       Impact factor: 12.779

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.