Sangadala S, Bhat U R, Mendicino J
Department of Biochemistry, University of Georgia, Athens 30602.
Mol Cell Biochem. 1992 Dec 2;118(1):75-90. doi: 10.1007/BF00249697.
Human respiratory mucin glycoproteins from patients with cystic fibrosis were purified and oligosaccharide chains were released by treatment with alkaline borohydride. A neutral oligosaccharide alditol fraction was isolated from mucin obtained from a patient with A blood group determinant by chromatography on DEAE-cellulose and individual oligosaccharide chains were then isolated by gel filtration on BioGel P-6 columns and high performance liquid chromatography with gradient and isocratic solvent systems. The structures of the purified oligosaccharides were determined by methylation analysis, sequential glycosidase digestion and 'H-NMR spectroscopy. The amount of each chain was determined by compositional analysis. A wide array of discrete branched oligosaccharide structures that contain from 3 to 22 sugar residues were found. Many of the oligosaccharides are related and appear to be precursors of larger chains. The predominant branched oligosaccharides which accumulate contain terminal blood group H (Fuc alpha 2Ga1 beta 4) or blood group A (Fuc alpha 2(Ga1NAc alpha 3) (Ga1 beta 4) determinants which stop further branching and chain elongation. The elongation of oligosaccharide chains in respiratory mucins occurs on the beta 3-linked G1cNAc at branch points, whereas the beta 6-linked G1cNAc residue ultimately forms short side chains with a Fuc alpha 2(Ga1NAc alpha 3) Ga1 beta 4 G1cNAc beta 6 structure in individuals with A blood group determinant. The results obtained in the current studies further suggest that even higher molecular weight oligosaccharide chains with analogous branched structures are present in some human respiratory mucin glycoproteins. Increasing numbers of the repeating sequence shown in the oligosaccharide below is present in the higher molecular weight chains. [formula: see text] This data in conjunction with our earlier observations on the extensive branching of these oligosaccharide chains helps to define and explain the enormous range of oligosaccharide structures found in human and swine respiratory mucin glycoproteins. Comparison of the relative concentrations of each oligosaccharide chain suggest that these oligosaccharides represent variations of a common branched core structure which may be terminated by the addition of alpha 2-linked fucose to the beta 3/4 linked galactose residue at each branch point. These chains accumulate and are found in the highest concentrations in these respiratory mucins.
对囊性纤维化患者的人呼吸道黏蛋白糖蛋白进行纯化,并通过碱性硼氢化物处理释放寡糖链。从具有A血型决定簇的患者的黏蛋白中通过DEAE - 纤维素柱色谱分离出中性寡糖糖醇级分,然后通过BioGel P - 6柱上的凝胶过滤和具有梯度和等度溶剂系统的高效液相色谱法分离出各个寡糖链。通过甲基化分析、顺序糖苷酶消化和'H - NMR光谱法确定纯化寡糖的结构。通过组成分析确定每条链的量。发现了一系列包含3至22个糖残基的离散分支寡糖结构。许多寡糖相互关联,似乎是较大链的前体。积累的主要分支寡糖含有末端血型H(Fucα2Galβ4)或血型A(Fucα2(GalNAcα3)(Galβ4)决定簇,它们阻止进一步的分支和链延长。呼吸道黏蛋白中寡糖链的延长发生在分支点处的β3连接的GlcNAc上,而β6连接的GlcNAc残基最终在具有A血型决定簇的个体中形成具有Fucα2(GalNAcα3)Galβ4GlcNAcβ6结构的短侧链。当前研究中获得的结果进一步表明,一些人呼吸道黏蛋白糖蛋白中存在具有类似分支结构的甚至更高分子量的寡糖链。在较高分子量的链中存在越来越多如下所示寡糖中的重复序列。[化学式:见原文] 这些数据与我们早期对这些寡糖链广泛分支的观察结果相结合,有助于定义和解释在人和猪呼吸道黏蛋白糖蛋白中发现的大量寡糖结构。每条寡糖链相对浓度的比较表明,这些寡糖代表了一种常见分支核心结构的变体,该结构可能通过在每个分支点向β3/4连接的半乳糖残基添加α2连接的岩藻糖而终止。这些链积累并在这些呼吸道黏蛋白中以最高浓度被发现。