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etramps, a new Plasmodium falciparum gene family coding for developmentally regulated and highly charged membrane proteins located at the parasite-host cell interface

机译:etramps,一种新的恶性疟原虫基因家族,编码位于寄生虫-宿主细胞界面的发育调控且带高电荷的膜蛋白

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摘要

After invasion of erythrocytes, the human malaria parasite Plasmodium falciparum resides within a parasitophorous vacuole and develops from morphologically and metabolically distinct ring to trophozoite stages. During these developmental phases, major structural changes occur within the erythrocyte, but neither the molecular events governing this development nor the molecular composition of the parasitophorous vacuole membrane (PVM) is well known. Herein, we describe a new family of highly cationic proteins from P. falciparum termed early transcribed membrane proteins (ETRAMPs). Thirteen members were identified sharing a conserved structure, of which six were found only during ring stages as judged from Northern and Western analysis. Other members showed different stage-specific expression patterns. Furthermore, ETRAMPs were associated with the membrane fractions in Western blots, and colocalization and selective permeabilization. studies demonstrated that ETRAMPs were located in the PVM. This was confirmed by immunoelectron microscopy where the PVM and tubovesicular extensions of the PVM were labeled. Early expressed ETRAMPs clearly defined separate PVM domains compared with the negatively charged integral PVM protein EXP-1, suggesting functionally different domains in the PVM with an oppositely charged surface coat. We also show that the dynamic change of ETRAMP composition in the PVM coincides with the morphological changes during development. The P. falciparum PVM is an important structure for parasite survival, and its analysis might provide better understanding of the requirements of intracellular parasites. [References: 71]
机译:入侵红细胞后,人类疟疾寄生虫恶性疟原虫就生活在一个寄生虫的液泡中,并从形态和代谢上不同的环发展为滋养体阶段。在这些发育阶段,红细胞内会发生主要的结构变化,但是众所周知,控制这种发育的分子事件和寄生虫液泡膜(PVM)的分子组成都不是众所周知的。在本文中,我们描述了恶性疟原虫的一种新的高度阳离子蛋白家族,称为早期转录膜蛋白(ETRAMPs)。根据北部和西部分析判断,确定了13个成员共有一个保守的结构,其中6个仅在环形阶段才发现。其他成员表现出不同的阶段特异性表达模式。此外,ETRAMPs与蛋白质印迹,共定位和选择性通透性中的膜部分有关。研究表明ETRAMP位于PVM中。免疫电子显微镜证实了这一点,其中标记了PVM和PVM的肾小管延伸。与带负电荷的完整PVM蛋白EXP-1相比,早期表达的ETRAMPs清楚地定义了单独的PVM结构域,表明具有带相反电荷的表面涂层的PVM中功能不同的结构域。我们还表明,PVM中ETRAMP成分的动态变化与发育过程中的形态变化相吻合。恶性疟原虫PVM是寄生虫生存的重要结构,其分析可能会更好地了解细胞内寄生虫的需求。 [参考:71]

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