Gerold P, Striepen B, Reitter B, Geyer H, Geyer R, Reinwald E, Risse H J, Schwarz R T
Zentrum für Hygiene und Medizinische Mikrobiologie, Philipps-Universität Marburg, Germany.
J Mol Biol. 1996 Aug 16;261(2):181-94. doi: 10.1006/jmbi.1996.0451.
The parasitic protozoan Trypanosoma congolense exhibits a dense surface coat which is pivotal for immunoevasion of the parasite. This dense surface coat is made of a single protein species, the variant surface glycoprotein, which is present in a high copy number. The protein is anchored to the plasma membrane by a glycosyl-phosphatidylinositol membrane anchor. A detailed study of the structure of T. congolense strain 423 (clone BENat 1.3) variant surface glycoprotein glycosyl-phosphatidylinositol membrane anchor was performed. Radioactively labelled core-glycan prepared by dephosphorylation, deamination and reduction was analysed by high-pH anion-exchange chromatography, size-exclusion and lectin affinity chromatography. Additionally the glycosyl-phosphatidylinositol membrane anchor core-glycan was purified from a bulk preparation of variant surface glycoprotein and subjected to mass spectrometry and methylation analysis. Using these methods we could identify a novel galactose-beta 1,6-N-acetyl-glucosamine-beta 1,4-branch modifying the mannose adjacent to the glucosamine of the mannose-alpha 1,2-mannose-alpha 1,6-mannose-alpha 1,4-glucosamine core-glycan of the variant surface glycoprotein glycosyl-phosphatidylinositol membrane anchor. Furthermore the biosynthetic pathway leading to this novel structure was investigated. Two putative glycosyl-phosphatidylinositol anchor precursors were identified having structures identical to the previously characterized Trypanosoma brucei brucei glycolipids P2 and P3 (also designated glycolipid A and C) consistent with a trimannosyl core and a dimyristoyl-glycerol. Both glycosyl-phosphatidylinositol anchor precursors of T. congolense do not possess the side-branch modification found on the mature protein membrane anchor, implying that the sugar side-chain is added to the anchor during its passage through the Golgi-apparatus.
寄生原生动物刚果锥虫具有一层致密的表面被膜,这对该寄生虫的免疫逃避至关重要。这层致密的表面被膜由单一蛋白质种类即可变表面糖蛋白构成,其以高拷贝数存在。该蛋白质通过糖基磷脂酰肌醇膜锚定连接到质膜上。对刚果锥虫423株(克隆BENat 1.3)可变表面糖蛋白糖基磷脂酰肌醇膜锚定的结构进行了详细研究。通过去磷酸化、脱氨和还原制备的放射性标记核心聚糖,采用高pH值阴离子交换色谱、尺寸排阻色谱和凝集素亲和色谱进行分析。此外,从可变表面糖蛋白的大量制备物中纯化糖基磷脂酰肌醇膜锚定核心聚糖,并进行质谱分析和甲基化分析。使用这些方法,我们能够鉴定出一种新的半乳糖-β1,6-N-乙酰葡糖胺-β1,4分支,它修饰了可变表面糖蛋白糖基磷脂酰肌醇膜锚定的甘露糖-α1,2-甘露糖-α1,6-甘露糖-α1,4-葡糖胺核心聚糖中与葡糖胺相邻的甘露糖。此外,还研究了导致这种新结构的生物合成途径。鉴定出两种假定的糖基磷脂酰肌醇锚定前体,其结构与先前表征的布氏布氏锥虫糖脂P2和P3(也称为糖脂A和C)相同,与三甘露糖核心和二肉豆蔻酰甘油一致。刚果锥虫的两种糖基磷脂酰肌醇锚定前体均不具有在成熟蛋白质膜锚定上发现的侧链修饰,这意味着糖侧链是在其通过高尔基体的过程中添加到锚定上的。