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来自刚地弓形虫的一族糖脂。刚地弓形虫糖基磷脂酰肌醇膜锚定物候选糖脂前体的鉴定。

A family of glycolipids from Toxoplasma gondii. Identification of candidate glycolipid precursor(s) for Toxoplasma gondii glycosylphosphatidylinositol membrane anchors.

作者信息

Tomavo S, Dubremetz J F, Schwarz R T

机构信息

Zentrum für Hygiene und Medizinische Mikrobiologie, Philipps-Universität Marburg, Germany.

出版信息

J Biol Chem. 1992 Jun 15;267(17):11721-8.

PMID:1534801
Abstract

Four major glycolipids were extracted from Toxoplasma gondii tachyzoites which were metabolically labeled with tritiated glucosamine, mannose, palmitic and myristic acid, ethanolamine, and inositol. Judging from their sensitivity to a set of enzymatic and chemical tests, these glycolipids share the following properties with the glycolipid moiety of the glycosylphosphatidylinositol anchor (GPI anchor) of the major surface protein, P30, of T. gondii: 1) a nonacetylated glucosamine-inositol phosphate linkage; 2) sensitivity toward phosphatidylinositol-specific phospholipase C and nitrous acid; 3) identity of HF-dephosphorylated GPI glycan backbone between three glycolipids and the HF-dephosphorylated core glycan of the GPI anchor of the major surface protein P30; 4) the presence of a linear core glycan structure blocked by an ethanolamine phosphate residue(s). Taken together with the nature of radiolabeled precursors incorporated into these glycolipids, the data indicate that these GPIs are involved in the biosynthesis of the GPI-membrane anchors of T. gondii.

摘要

从经氚标记的葡糖胺、甘露糖、棕榈酸和肉豆蔻酸、乙醇胺及肌醇进行代谢标记的刚地弓形虫速殖子中提取出四种主要糖脂。从它们对一系列酶促和化学测试的敏感性判断,这些糖脂与刚地弓形虫主要表面蛋白P30的糖基磷脂酰肌醇锚(GPI锚)的糖脂部分具有以下共同特性:1)非乙酰化的葡糖胺 - 肌醇磷酸键;2)对磷脂酰肌醇特异性磷脂酶C和亚硝酸敏感;3)三种糖脂的HF - 去磷酸化GPI聚糖主链与主要表面蛋白P30的GPI锚的HF - 去磷酸化核心聚糖相同;4)存在被磷酸乙醇胺残基阻断的线性核心聚糖结构。结合掺入这些糖脂的放射性标记前体的性质,数据表明这些GPI参与了刚地弓形虫GPI - 膜锚的生物合成。

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Extracellular Toxoplasma gondii tachyzoites metabolize and incorporate unnatural sugars into cellular proteins.细胞外的刚地弓形虫速殖子代谢并将非天然糖类掺入细胞蛋白质中。
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Virulent and avirulent strains of Toxoplasma gondii which differ in their glycosylphosphatidylinositol content induce similar biological functions in macrophages.
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