Couto A S, De Lederkremer R M, Colli W, Alves M J
Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina.
Eur J Biochem. 1993 Oct 15;217(2):597-602. doi: 10.1111/j.1432-1033.1993.tb18282.x.
The Tc-85 glycoprotein, specific for the infective stage of Trypanosoma cruzi, is anchored via glycosylphosphatidylinositol. The protein was purified from parasites, labeled metabolically with palmitic acid, by immunoprecipitation with the H1A10 monoclonal antibody or by affinity column chromatography on wheat germ agglutinin. Antisera to the soluble form of the variant surface glycoprotein of Trypanosoma brucei brucei cross-reacted with Tc-85 when the immunoprecipitate was analysed by Western blotting. The reaction was intensified upon previous incubation of the glycoprotein with phosphatidylinositol-specific phospholipase C. Such recognition was abolished when the cyclic phosphate was opened by mild acid treatment. The lipid cleaved by phospholipase C digestion, was identified as 1-O-hexadecylglycerol by reverse-phase thin-layer chromatography. The glycan core was deaminated and chemically labeled by reduction with NaB3H4. The labeled glycoprotein was exhaustively treated with pronase and dephosphorylated with 50% HF. Although microheterogeneity of the oligosaccharide moiety was apparent, by thin layer chromatography, a main spot coincident with Man(alpha 1-2) Man(alpha 1-6) Man(alpha 1-4) anhydromannitol was shown, consistent with the conserved core structure of all glycosylphosphatidylinositol anchors analysed to date.
针对克氏锥虫感染阶段具有特异性的Tc - 85糖蛋白通过糖基磷脂酰肌醇进行锚定。该蛋白从寄生虫中纯化得到,通过用棕榈酸进行代谢标记、用H1A10单克隆抗体进行免疫沉淀或在麦胚凝集素上进行亲和柱层析。当通过蛋白质印迹分析免疫沉淀物时,布氏布氏锥虫可变表面糖蛋白可溶性形式的抗血清与Tc - 85发生交叉反应。在用磷脂酰肌醇特异性磷脂酶C预先孵育糖蛋白后,反应增强。当通过温和酸处理打开环状磷酸酯时,这种识别被消除。通过反相薄层层析鉴定,经磷脂酶C消化裂解的脂质为1 - O - 十六烷基甘油。聚糖核心经脱氨并用NaB3H4还原进行化学标记。标记的糖蛋白用链霉蛋白酶彻底处理并用50% HF去磷酸化。尽管通过薄层层析可明显看出寡糖部分存在微不均一性,但显示出一个与Man(α1 - 2)Man(α1 - 6)Man(α1 - 4)脱水甘露糖醇一致的主要斑点,这与迄今为止分析的所有糖基磷脂酰肌醇锚定物的保守核心结构相符。