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PMID: 427632 Published · ppublish English Journal Article

A structural basis for four distinct elution profiles on concanavalin A--Sepharose affinity chromatography of glycopeptides.

Canadian journal of biochemistry ·Vol. 57 ·No. 1 ·1979-01-00 ·Pages 83-96

Narasimhan S, Wilson JR, Martin E, Schachter H

Abstract

Twelve 14C-acetylated glycopeptides have been subjected to affinity chromatography on concanvalin A (Con A)--Sepharose at pH 7.5. The elution profiles could be classified into four distinct patterns. The first pattern showed no retardation of glycopeptide on the column and was elicited with a glycopeptide having three peripheral oligosaccharide chains: (abstract:see text). Such glycopeptides have only a single mannose residue capable of interacting with Con A--Sepharose; an interacting mannose residue is either an alpha-linked nonreducing terminal residue or an alpha-linked 2-O-substituted residue. The second type of profile showed a retarded elution of glycopeptide with buffer lacking methyl alpha-D-glucopyranoside (indicative of weak interaction with the column) and was given by glycopeptides with the structures: (abstract: see text) where R1 is either H or a sialyl residue. The third profile type showed tight binding of glycopeptide to Con A--Sepharose and elution as a sharp peak with 0.1 M methyl alpha-D-glucopyranoside; glycopeptides giving this pattern had the structures: (abstract: see text) where R2 is either H, glcNAc, Gal-beta 1,4-GlcNAc, or sialyl-Gal-beta 1,4-GlcNAc. These glycopeptides all have two interacting mannose residues, the mimimum required for binding to the column; one of these mannose residues must, however, be a terminal residue to obtain tight binding and sharp elution. The fourth profile type showed tight binding of glycopeptide to the column but elution with 0.1 M methyl alpha-D-glucopyranoside resulted in a broad peak indicating very tight binding; glycopeptides showing this behaviour had the structures: (abstract: see text) where R3 is either GlcNAc,Gal-beta 1,4-GlcNAc, or sialyl-Gal-beta 1,4-GlcNAc. Therefore it can be concluded that although a minimum of two interacting mannose residues is required for binding to Con A--Sepharose, the residues linked to these mannoses can either strengthen or weaken binding to the column.

MeSH Terms
Carbohydrates/analysis Chromatography, Affinity/methods Concanavalin A Glycopeptides/isolation & purification Humans Immunoglobulin G Molecular Conformation Multiple Myeloma/immunology Sepharose
Chemicals
Carbohydrates Glycopeptides Immunoglobulin G Concanavalin A Sepharose
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Narasimhan S
Wilson J R
Martin E
Schachter H
Article Info
Journal
Canadian journal of biochemistry
Abbr.
Can J Biochem
ISSN
0008-4018
Published
1979-01-00
Pages
83-96
Language
English
Region
Canada
NLM ID
0421034
Subset
IM
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