Narasimhan S, Wilson J R, Martin E, Schachter H
Can J Biochem. 1979 Jan;57(1):83-96. doi: 10.1139/o79-011.
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.
12种14C - 乙酰化糖肽在pH 7.5条件下于伴刀豆球蛋白A(Con A)-琼脂糖上进行亲和层析。洗脱图谱可分为四种不同模式。第一种模式显示糖肽在柱上无滞留,由一种带有三条外周寡糖链的糖肽引发(摘要:见正文)。这类糖肽仅有一个能够与Con A - 琼脂糖相互作用的甘露糖残基;一个相互作用的甘露糖残基要么是α - 连接的非还原末端残基,要么是α - 连接的2 - O - 取代残基。第二种洗脱图谱类型显示在缺乏α - D - 甲基吡喃葡萄糖苷的缓冲液中糖肽洗脱延迟(表明与柱的相互作用较弱),由具有以下结构的糖肽给出(摘要:见正文),其中R1为H或一个唾液酸残基。第三种图谱类型显示糖肽与Con A - 琼脂糖紧密结合,并在0.1 Mα - D - 甲基吡喃葡萄糖苷作用下以尖锐峰洗脱;给出这种模式的糖肽具有以下结构(摘要:见正文),其中R2为H、N - 乙酰葡糖胺、半乳糖 - β1,4 - N - 乙酰葡糖胺或唾液酸 - 半乳糖 - β1,4 - N - 乙酰葡糖胺。这些糖肽都有两个相互作用的甘露糖残基,这是与柱结合所需的最少数量;然而,这些甘露糖残基中的一个必须是末端残基才能实现紧密结合和尖锐洗脱。第四种图谱类型显示糖肽与柱紧密结合,但用0.1 Mα - D - 甲基吡喃葡萄糖苷洗脱时产生宽峰,表明结合非常紧密;表现出这种行为的糖肽具有以下结构(摘要:见正文),其中R3为N - 乙酰葡糖胺、半乳糖 - β1,4 - N - 乙酰葡糖胺或唾液酸 - 半乳糖 - β1,4 - N - 乙酰葡糖胺。因此可以得出结论,虽然与Con A - 琼脂糖结合至少需要两个相互作用的甘露糖残基,但与这些甘露糖相连的残基可以增强或减弱与柱的结合。