Back to Search Start Over

ABH blood group antigens in N-glycan of human glycophorin A.

Authors :
Fredriksson SA
Podbielska M
Nilsson B
Krotkiewska B
Lisowska E
Krotkiewski H
Source :
Archives of biochemistry and biophysics [Arch Biochem Biophys] 2010 Jun 15; Vol. 498 (2), pp. 127-35. Date of Electronic Publication: 2010 Apr 29.
Publication Year :
2010

Abstract

We previously showed that a small proportion of the O-linked oligosaccharide chains of human glycophorin A (GPA) contains blood group A, B or H antigens, relevant to the ABO phenotype of the donor. The structures of these minor O-glycans have been established (Podbielska et al. (2004) [20]). By the use of immunochemical methods we obtained results indicating that ABH blood group epitopes are also present in N-glycan of human GPA (Podbielska and Krotkiewski (2000) [22]). In the present paper we report a detailed analysis of GPA N-glycans using nanoflow electrospray ionization tandem mass spectrometry. N-glycans containing A-, B- and H-related sequences were identified in GPA preparations obtained from erythrocytes of blood group A, B and O donors, respectively. The ABH blood group epitopes are present on one antenna of the N-glycan, whereas a known sialylated sequence NeuAcalpha2-6Galbeta1-4GlcNAc- occurs on the other antenna and other details are in agreement with the known major structure of the GPA N-glycan. In the bulk of the biantennary sialylated N-glycans released from GPA preparations, the blood group ABH epitopes-containing N-glycans, similarly O-glycans, constituted only a minor part. The amount relative to other N-glycans was estimated to 2-6% of blood group H epitope-containing glycans released from GPA-O preparations and 1-2% of blood group A and B epitope-containing glycans, released from GPA-A and GPA-B, respectively.<br /> (Copyright (c) 2010 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1096-0384
Volume :
498
Issue :
2
Database :
MEDLINE
Journal :
Archives of biochemistry and biophysics
Publication Type :
Academic Journal
Accession number :
20434428
Full Text :
https://doi.org/10.1016/j.abb.2010.04.017