The antigenic determinants recognized by three monoclonal antibodies to keratan sulphate involve sulphated hepta- or larger oligosaccharides of the poly(N-acetyllactosamine) series
Open Access
- 1 June 1986
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 157 (2) , 385-391
- https://doi.org/10.1111/j.1432-1033.1986.tb09680.x
Abstract
The carbohydrate determinants of keratan sulphate recognized by three monoclonal antibodies (5-D-4, 1-B-4 and MZ15) have been investigated by solid-phase radioimmunoassay using bovine corneal keratan sulphate as the immobilized reference antigen. The antibodies appeared highly specific for sulphated poly(N-acetyllactosamine) sequences, for their binding was strongly inhibited by preparations of keratan sulphate, but not by glycoproteins with non-sulphated poly(N-acetyllactosamine) sequences of I and i antigen types, a desulphated keratan sulphate hexasaccharide, an array of neutral and sulphated mono- and disaccharides and other glycosaminoglycans. Inhibition of binding assays using a series of structurally characterized sulphated di, tetra-, hexa-, octa- and decasaccharides, and partially characterized larger oligosaccharides, isolated from bovine corneal keratan sulphate after digestion with endo-β-galactosidase (see preceding two papers in this journal) showed that the smallest oligosaccharide reactive with all three antibodies was the linear pentasulphated hexasaccharide, E-II although antibody 1-B-4 reacted with a tetrasulphated analogue. The heptasulphated octasaccharide, G-III, was more active; among the structurally characterized keratan sulphate oligosaccharides the nonasulphated decasaccharide, I-IV, was the most active. Thus, the hepta- and octasaccharide sequences, indicated by brackets below are proposed as candidate antigenic structures recognized by the three monoclonal antibodies. Antibody 5-D-4 differs from the other two antibodies in reacting relatively strongly with a minor oligosaccharide which chromatographs as a hexasulphated octasaccharide, G-I, and most strongly with a minor sulphated, linear dodecasaccharide, J-II, which has been partially characterized [Tang, P. W., Scudder, P., Mehmet, H., Hounsell, E. F. & Feizi, T., unpublished results] and may contain N-sulphated glucosamine residues.This publication has 31 references indexed in Scilit:
- Novel approach to the study of the antigenicities and receptor functions of carbohydrate chains of glycoproteinsBiochemical and Biophysical Research Communications, 1985
- The carbohydrate specificities of the monoclonal antibodies 29.1, 445 and 3C1B12 to the epidermal growth factor receptor of A431 cellsBioscience Reports, 1985
- Changes in proteoglycan composition of F9 teratocarcinoma cells upon differentiationEuropean Journal of Biochemistry, 1983
- A multiplicity of erythrocyte glycolipids of the neolacto series revealed by immuno-thin-layer chromatography with monoclonal anti-I and anti-i antibodiesBioscience Reports, 1983
- Evidence for the occurrence of O-glycosidically linked oligosaccharides of poly-N-acetyllactosamine type on the human leucocyte common antigenBiochemical and Biophysical Research Communications, 1983
- Marker of peripheral blood granulocytes and monocytes of man recognized by two monoclonal antibodies VEP8 and VEP9 involves the trisaccharide 3‐fucosyl‐N‐acetyllactosamineEuropean Journal of Immunology, 1982
- The monoclonal antibody anti‐SSEA‐1 discriminates between fucosylated type 1 and type 2 blood group chainsFEBS Letters, 1981
- Changes in the expression and polarization of blood group I and i antigens in post-implantation embryos and teratocarcinomas of mouse associated with cell differentiationExperimental Cell Research, 1981
- A radioimmunoassay for the measurement of blood group Ii activities: Its application to glycoconjugates, oligosaccharides and intact cellsMolecular Immunology, 1979
- Conformation of keratan sulphateJournal of Molecular Biology, 1974