Details

Autor(en) / Beteiligte

• Endo, T
• Ohbayashi, H
• Kanazawa, K
• Kochibe, N
• Kobata, A

Titel

Carbohydrate binding specificity of immobilized Psathyrella velutina lectin

Ist Teil von

• The Journal of biological chemistry, 1992-01, Vol.267 (2), p.707-713

Ort / Verlag

Bethesda, MD: Elsevier Inc

Erscheinungsjahr

1992

Quelle

MEDLINE

Beschreibungen/Notizen

• The carbohydrate binding specificity of Psathyrella velutina lectin (PVL) was thoroughly investigated by analyzing the behavior of various complex-type oligosaccharides and human milk oligosaccharides on a PVL-Affi-Gel 10 column. Basically, the lectin interacts with the nonreducing terminal beta-N-acetylglucosamine residue, but does not show any affinity for the nonreducing terminal N-acetylgalactosamine or N-acetylneuraminic acid residue. Substitution of the terminal N-acetylglucosamine residues of oligosaccharides by galactose completely abolishes their affinity to the column. GlcNAc beta 1→3Gal beta 1→4sorbitol binds to the column, but GlcNAc beta 1→6Gal beta 1→4sorbitol is only retarded in the column. The behavior of degalactosylated N-linked oligosaccharides is quite interesting. Although all degalactosylated monoantennary sugar chain isomers are retarded in the column, those with the GlcNAc beta 1→2Man group interact more strongly with the column than those with the GlcNAc beta 1→4Man group or the GlcNAc beta 1→6Man group. The degalactosylated bi- and triantennary sugar chains bind to the column, but the tetraantennary ones are only retarded in the column. These results indicated that the binding affinity is not simply determined by the number of terminal N-acetylglucosamine residues. Addition of the bisecting N-acetylglucosamine residue reduces the affinity of oligosaccharides to the column, but addition of an alpha-fucosyl residue at the C-6 position of the proximal N-acetylglucosamine residue does not affect the behavior of oligosaccharides in the column. These results indicated that the binding specificity of PVL is quite different from those of other N-acetylglucosamine-binding lectins from higher plants, which interact preferentially with the GlcNAc beta 1→4 residue.