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布氏锥虫的原环素缺失突变体在其表面表达游离的糖基磷脂酰肌醇。

Procyclin null mutants of Trypanosoma brucei express free glycosylphosphatidylinositols on their surface.

作者信息

Vassella Erik, Bütikofer Peter, Engstler Markus, Jelk Jennifer, Roditi Isabel

机构信息

Institut für Zellbiologie, Universität Bern, CH-3012 Bern, Switzerland.

出版信息

Mol Biol Cell. 2003 Apr;14(4):1308-18. doi: 10.1091/mbc.e02-10-0694.

Abstract

Procyclins are abundant, glycosylphosphatidylinositol (GPI)-anchored proteins on the surface of procyclic (insect) form trypanosomes. To investigate whether trypanosomes are able to survive without a procyclin coat, all four procyclin genes were deleted sequentially. Bloodstream forms of the null mutant exhibited no detectable phenotype and were able to differentiate to procyclic forms. Initially, differentiated null mutant cells were barely able to grow, but after an adaptation period of 2 mo in culture they proliferated at the same rate as wild-type trypanosomes. Analysis of these culture-adapted null mutants revealed that they were covered by free GPIs. These were closely related to the mature procyclin anchor in structure and were expressed on the surface in numbers comparable with that of procyclin in wild-type cells. However, free GPIs were smaller than the procyclin anchor, indicative of a lower number of poly-N-acetyllactosamine repeats, and a proportion contained diacylphosphatidic acid. Free GPIs are also expressed by wild-type cells, although to a lesser extent. These have been overlooked in the past because they partition in a solvent fraction (chloroform/water/methanol) that is normally discarded when GPI-anchored proteins are purified.

摘要

前环素是前循环型(昆虫型)锥虫表面丰富的糖基磷脂酰肌醇(GPI)锚定蛋白。为了研究锥虫在没有前环素包被的情况下是否能够存活,依次删除了所有四个前环素基因。缺失突变体的血流型未表现出可检测到的表型,并且能够分化为前循环型。最初,分化的缺失突变体细胞几乎无法生长,但在培养2个月的适应期后,它们以与野生型锥虫相同的速率增殖。对这些适应培养的缺失突变体的分析表明,它们被游离的GPI覆盖。这些在结构上与成熟的前环素锚密切相关,并且在表面上的表达数量与野生型细胞中的前环素相当。然而,游离的GPI比前环素锚小,表明多聚N-乙酰乳糖胺重复序列的数量较少,并且一部分含有二酰基磷脂酸。野生型细胞也表达游离的GPI,尽管程度较低。过去这些被忽视了,因为它们分配在一个溶剂组分(氯仿/水/甲醇)中,而在纯化GPI锚定蛋白时通常会丢弃该组分。

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