Previato J O, Jones C, Xavier M T, Wait R, Travassos L R, Parodi A J, Mendonça-Previato L
Departamento de Microbiologia Geral, Universidade Federal do Rio de Janeiro, Brazil.
J Biol Chem. 1995 Mar 31;270(13):7241-50. doi: 10.1074/jbc.270.13.7241.
We have investigated the structure of the glycosylphosphatidylinositol (GPI) anchor and the O-linked glycan chains of the 40/45-kDa glycoprotein from the cell surface of the protozoan parasite Trypanosoma cruzi. This glycoconjugate is the major acceptor for sialic acid transferred by trans-sialidase of T. cruzi Y-strain, epimastigote form. The GPI anchor was liberated by treatment with hot alkali, and the phosphoinositol-oligosaccharide moiety was characterized and shown to have the following structure. [formula: see text] Unusually the glucosamine was 6-O-substituted with 2-aminoethylphosphonate, and 2-aminoethylphosphonate was also present on the third mannose residue distal to glucosamine, partially replacing the ethanolamine phosphate. The beta-eliminated reduced oligosaccharide chains showed that two novel classes of O-linked N-acetylglucosamine oligosaccharide were present. The first series had the structures Galp beta 1-3GlcNAc-ol; Galp beta 1-6(Galp beta 1-3)GlcNAc-ol; and Galp beta 1-2Galp beta 1-6(Galp beta 1-3)GlcNAc-ol, whereas the other series had a 1-4 linkage to N-acetylglucosaminitol and had structures Galp beta 1-4GlcNAc-ol, Galp beta 1-6(Galp beta 1-4)GlcNAc-ol, and Galp beta 1-2Galp beta 1-6(Galp beta 1-4)GlcNAc-ol. We have also investigated the kinetics of in vitro sialylation of these O-linked oligosaccharides by the T. cruzi transsialidase and have shown that incorporation of one molecule of sialic acid hinders entry of a second molecule when two potential acceptor sites are present.
我们研究了原生动物寄生虫克氏锥虫细胞表面40/45-kDa糖蛋白的糖基磷脂酰肌醇(GPI)锚和O-连接聚糖链的结构。这种糖缀合物是克氏锥虫Y株(前鞭毛体形式)的转唾液酸酶转移唾液酸的主要受体。通过热碱处理释放GPI锚,并对磷酸肌醇寡糖部分进行了表征,结果表明其具有以下结构。[化学式:见原文] 不同寻常的是,葡糖胺的6-O位被2-氨基乙基膦酸酯取代,并且在葡糖胺远端的第三个甘露糖残基上也存在2-氨基乙基膦酸酯,部分取代了磷酸乙醇胺。β-消除还原的寡糖链表明存在两类新型的O-连接的N-乙酰葡糖胺寡糖。第一系列具有以下结构:Galpβ1-3GlcNAc-ol;Galpβ1-6(Galpβ1-3)GlcNAc-ol;和Galpβ1-2Galpβ1-6(Galpβ1-3)GlcNAc-ol,而另一系列与N-乙酰葡糖胺醇具有1-4连接,并且具有以下结构:Galpβ1-4GlcNAc-ol;Galpβ1-6(Galpβ1-4)GlcNAc-ol;和Galpβ1-2Galpβ1-6(Galpβ1-4)GlcNAc-ol。我们还研究了克氏锥虫转唾液酸酶对这些O-连接寡糖进行体外唾液酸化的动力学,并表明当存在两个潜在的受体位点时,一个唾液酸分子的掺入阻碍了第二个分子的进入。