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Blood groups A determinant

Prevalence in Asian Strains The Lewis A, B, D, and Blood-Group A Determinants 130... [Pg.99]

Fuc(al-4) were also observed in A. maculatum (Fig. 4). Other unusual sequences, namely the dimer H epitope Fuc(al-2)Gal(Pl-3)[Fuc(al—2)]Gal, and blood group A determinant terminated with an additional a-l,3-linked GlcNAc unit, were found in X. laevis (Fig. 5). [Pg.167]

The rational design of glycosyltransferase inhibitors has been on substrate mimicry. For example, Lowary and coworkers synthesized 3-amino-3-deoxy(Fucal-2)Gal/3-0(CH2)7CH3 as a competitive inhibitor of the blood group A A-acetylgalactosaminyltransferase (Figure 16(i)). The administration of this compound to cells afforded only a modest reduction of the blood group A determinant expression, which was attributed to... [Pg.280]

Figure 25.12 Structures of the A, B, and 0 blood-group antigenic determinants. Figure 25.12 Structures of the A, B, and 0 blood-group antigenic determinants.
Kukowsaka-Fatallo, J. F., R. D. Farsen, R. P. Nair, and J. B. Fowe, A cloned human cDNA determines expression of a mouse stage-specific embryonic antigen and the Lewis blood group a(l,3/l,4)fucosyltransferase. Genes Dev. 4 1288-1303, 1990. [Pg.376]

Ten sialic-acid-containing oligosaccharides and four neutral oligosaccharides have been purified from the major glycoprotein fraction of hog, submaxillary-gland mucin. H-N.m.r. spectroscopy at 360 MHz, in combination with methylation analysis and mass spectrometry, allowed the determination of their structures, which are partial structures of a pentasaccharide (see Fig. 42) having blood-group A activity.221... [Pg.218]

Paulsen and co-workers [191] synthesised the trisaccharide (263) representing the afucosyl end group of the blood-group A (type 1) determinant from the disaccharide (264). This was acetylated and deacetonated and the product converted into the acetate (265) via the 3, 4 -orthoacetate. Condensation of (265) with the azido-chloride (237) in the presence of silver perchlorate gave the a-linked trisaccharide (266) which was deprotected to give (263). [Pg.109]

The Lewis a (Lea) blood-group trisaccharide determinant (345) first synthesised by Lemieux and co-workers [25] was also prepared by Sinay and co-workers [222] using the imidate procedure [232]. Condensation of the fucosyl imidate (321) with the disaccharide (346), prepared via the allyl ether (347), in the presence of toluene p-... [Pg.118]

G. Schiffman, E. A. Kabat, and W. Thompson, Immunochemical studies on blood groups. XXXn. Immunochemical properties of and possible partial structures for the blood group A, B, and H antigenic determinants, Biochem. J., 3 (1964) 587-593. [Pg.139]

The Chemical Synthesis of 2-Acetamido-2-deoxy-4-(3-(a-L-fucopyra-nosyl)-3-<9-(/l-D-galactopyranosyl)-D-glucose. The Lewis a Blood-Group Antigenic Determinant, R. U. Lemieux and H. Driguez, J. Am. Chem. Soc., 97 (1975) 4063 1069. [Pg.23]

The first physico-chemical determination appears to be that of Kekwick.116 He examined in the ultracentrifuge the material prepared from ovarian cyst fluid which showed blood-group A specificity.117 This product was electrophoretically homogeneous and only one component was apparent in the sedimentation measurements. The complex was moderately polydisperse and possessed a highly asymmetric shape (f/fo = 3.2). The values of the sedimentation and diffusion constants, interpolated graphically at a given concentration, corresponded to a mean molecular weight of 260,000... [Pg.327]

Structurally, the O-polysaccharide chains of H. pylori clinical isolates have a poly-A-acetyl-lactosamine (-LacNAc) chain decorated with multiple lateral a-L-fucose residues forming internal Lex determinants with terminal Lex or Ley units (Fig. 10.4) or, in some strains with additional, D-glucose or D-galactose residues (Moran 2001 a,b, 2008 Monteiro, 2001). Moreover, Lea, Leb, sialyl-Lex, and H-1 antigens have been structurally described in other strains, as well as the related blood groups A and B (Fig. 10.4), but occur in association with Lex and LacNAc chains (Monteiro et al., 2000a,b Heneghan et al., 2000). [Pg.219]

The procedure has been employed for the synthesis of the determinant trisaccharide unit of the human blood group A using 2-28 and the (-)-menthyl glyoxylate 2-27 as a matched pair to give the desired disaccharide 2-30 after isomerisation of the primarily obtained mixture of 2-29 and 2-30. [Pg.17]


See other pages where Blood groups A determinant is mentioned: [Pg.87]    [Pg.158]    [Pg.161]    [Pg.162]    [Pg.288]    [Pg.1781]    [Pg.298]    [Pg.87]    [Pg.158]    [Pg.161]    [Pg.162]    [Pg.288]    [Pg.1781]    [Pg.298]    [Pg.618]    [Pg.22]    [Pg.359]    [Pg.142]    [Pg.50]    [Pg.53]    [Pg.470]    [Pg.127]    [Pg.319]    [Pg.260]    [Pg.182]    [Pg.242]    [Pg.344]    [Pg.344]    [Pg.358]    [Pg.360]    [Pg.215]    [Pg.57]    [Pg.77]    [Pg.105]    [Pg.108]    [Pg.162]    [Pg.172]    [Pg.182]    [Pg.103]    [Pg.227]    [Pg.432]    [Pg.36]   
See also in sourсe #XX -- [ Pg.1781 ]




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