Conzelmann A, Kornfeld S
J Biol Chem. 1984 Oct 25;259(20):12528-35.
The O-linked oligosaccharides of the cloned, murine cytotoxic T cell line B6.1.SF.1 were compared with the corresponding oligosaccharides from a Vicia villosa lectin-resistant mutant of B6.1.SF.1 called VV6 (Conzelmann, A., Pink, R., Acuto, O., Mach, J.-P., Dolivo, S., and Nabholz, M. (1980) Eur. J. Immunol. 10, 860-868). The VV6 mutant cells are deficient in binding sites for this GalNAc-specific lectin. Cells were grown in the presence of [3H]glucosamine and [3H] galactose to label the glycoproteins, and the desialyzed, alkaline borohydride-released oligosaccharides were isolated and characterized. The VV6 cells contained a series of O-linked oligosaccharides ranging in size from a disaccharide to a pentasaccharide. These were composed of galactose, N-acetylglucosamine, and N-acetylhexosaminitol, the latter sugar being derived from the reducing terminus. The predominant oligosaccharide had the partial structure Gal beta GlcNAc beta-(Gal beta)N-acetylhexosaminitol. In contrast, the analogous oligosaccharides of the parental cells contained additional beta-linked GalNAc residues located at nonreducing termini. The smallest of these had the structure GalNAc beta 1,4Gal beta-N-acetylhexosaminitol. Neither cell line contained significant amounts of terminal GalNAc linked to Ser/Thr which is the main binding site for the V. villosa B4 lectin on Tn erythrocytes (Tollefsen, S. R., and Kornfeld, R. (1983) J. Biol. Chem. 258, 5172-5176). These findings suggest that the major binding sites for the V. villosa lectin on the parental cytotoxic T cell line consist of structures containing beta 1,4-linked GalNAc residues at the nonreducing ends of conventional O-linked structures. The VV6 cells lack these beta-linked GalNAc residues, and this may account for their deficiency of V. villosa lectin-binding sites. In the following paper (Conzelmann, A., and Kornfeld, S. (1984) J. Biol. Chem. 259, 12536-12542), we demonstrate that the VV6 cells are missing the N-acetylgalactosaminyltransferase that is responsible for the synthesis of these unusual oligosaccharides.
将克隆的小鼠细胞毒性T细胞系B6.1.SF.1的O-连接寡糖与来自B6.1.SF.1的绒毛野豌豆凝集素抗性突变体VV6(Conzelmann,A.,Pink,R.,Acuto,O.,Mach,J.-P.,Dolivo,S.和Nabholz,M.(1980)Eur. J. Immunol. 10,860 - 868)的相应寡糖进行了比较。VV6突变体细胞缺乏这种GalNAc特异性凝集素的结合位点。细胞在[3H]葡糖胺和[3H]半乳糖存在下生长以标记糖蛋白,然后分离并表征经脱唾液酸、碱性硼氢化钠释放的寡糖。VV6细胞含有一系列大小从二糖到五糖的O-连接寡糖。它们由半乳糖、N-乙酰葡糖胺和N-乙酰己糖胺醇组成,后一种糖来自还原端。主要的寡糖具有部分结构GalβGlcNAcβ-(Galβ)N-乙酰己糖胺醇。相比之下,亲代细胞的类似寡糖在非还原端含有额外的β-连接的GalNAc残基。其中最小的具有结构GalNAcβ1,4Galβ-N-乙酰己糖胺醇。两种细胞系均不含有与Ser/Thr连接的大量末端GalNAc,而Ser/Thr是Tn红细胞上绒毛野豌豆B4凝集素的主要结合位点(Tollefsen,S. R.和Kornfeld,R.(1983)J. Biol. Chem. 258,5172 - 5176)。这些发现表明,绒毛野豌豆凝集素在亲代细胞毒性T细胞系上的主要结合位点由在常规O-连接结构的非还原端含有β1,4-连接的GalNAc残基的结构组成。VV6细胞缺乏这些β-连接的GalNAc残基,这可能解释了它们缺乏绒毛野豌豆凝集素结合位点的原因。在接下来的论文中(Conzelmann,A.和Kornfeld,S.(1984)J. Biol. Chem. 259,12536 - 12542),我们证明VV6细胞缺失了负责合成这些异常寡糖的N-乙酰半乳糖胺基转移酶。