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etramps,一个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度电荷的膜蛋白。

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

作者信息

Spielmann Tobias, Fergusen David J P, Beck Hans-Peter

机构信息

Department of Medical Parasitology and Infection Biology, Swiss Tropical Institute, Basel CH 4002, Switzerland.

出版信息

Mol Biol Cell. 2003 Apr;14(4):1529-44. doi: 10.1091/mbc.e02-04-0240.

DOI:10.1091/mbc.e02-04-0240
PMID:12686607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC153120/
Abstract

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.

摘要

人类疟原虫恶性疟原虫侵入红细胞后,寄生于一个寄生泡内,并从形态和代谢上不同的环状阶段发育为滋养体阶段。在这些发育阶段,红细胞内会发生重大的结构变化,但控制这种发育的分子事件以及寄生泡膜(PVM)的分子组成都尚不明确。在此,我们描述了一个来自恶性疟原虫的新的高阳离子蛋白家族,称为早期转录膜蛋白(ETRAMPs)。鉴定出13个成员具有保守结构,根据Northern和Western分析判断,其中6个仅在环状阶段被发现。其他成员表现出不同的阶段特异性表达模式。此外,在Western印迹中ETRAMPs与膜组分相关,共定位和选择性通透研究表明ETRAMPs位于PVM中。免疫电子显微镜证实了这一点,其中PVM及其管状泡状延伸被标记。与带负电荷的整合PVM蛋白EXP-1相比,早期表达的ETRAMPs清楚地界定了不同的PVM结构域,这表明PVM中存在功能不同的结构域,其表面包被带相反电荷。我们还表明,PVM中ETRAMP组成的动态变化与发育过程中的形态变化一致。恶性疟原虫的PVM是寄生虫生存的重要结构,对其分析可能有助于更好地理解细胞内寄生虫的需求。

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本文引用的文献

1
Secretory transport in Plasmodium.疟原虫中的分泌运输
Parasitol Today. 1993 Mar;9(3):98-102. doi: 10.1016/0169-4758(93)90216-3.
2
Genome sequence of the human malaria parasite Plasmodium falciparum.人类疟原虫恶性疟原虫的基因组序列。
Nature. 2002 Oct 3;419(6906):498-511. doi: 10.1038/nature01097.
3
Infectivity-associated changes in the transcriptional repertoire of the malaria parasite sporozoite stage.疟原虫子孢子阶段转录组中与感染性相关的变化。
J Biol Chem. 2002 Nov 1;277(44):41948-53. doi: 10.1074/jbc.M207315200. Epub 2002 Aug 12.
4
The malaria-infected red blood cell: structural and functional changes.感染疟疾的红细胞:结构与功能变化
Adv Parasitol. 2001;50:1-86. doi: 10.1016/s0065-308x(01)50029-9.
5
PlasmoDB: the Plasmodium genome resource. An integrated database providing tools for accessing, analyzing and mapping expression and sequence data (both finished and unfinished).疟原虫数据库(PlasmoDB):疟原虫基因组资源。一个集成数据库,提供用于访问、分析以及绘制表达和序列数据(包括完整和不完整数据)的工具。
Nucleic Acids Res. 2002 Jan 1;30(1):87-90. doi: 10.1093/nar/30.1.87.
6
Trafficking and assembly of the cytoadherence complex in Plasmodium falciparum-infected human erythrocytes.恶性疟原虫感染的人类红细胞中细胞黏附复合物的运输与组装
EMBO J. 2001 Oct 15;20(20):5636-49. doi: 10.1093/emboj/20.20.5636.
7
Evidence for a role for a Plasmodium falciparum homologue of Sec31p in the export of proteins to the surface of malaria parasite-infected erythrocytes.恶性疟原虫Sec31p同源物在蛋白质向疟原虫感染红细胞表面输出中作用的证据。
J Cell Sci. 2001 Sep;114(Pt 18):3377-86. doi: 10.1242/jcs.114.18.3377.
8
The Toxoplasma gondii protein ROP2 mediates host organelle association with the parasitophorous vacuole membrane.弓形虫蛋白ROP2介导宿主细胞器与寄生泡膜的结合。
J Cell Biol. 2001 Jul 9;154(1):95-108. doi: 10.1083/jcb.200101073.
9
Evaluation of methods for the prediction of membrane spanning regions.膜跨越区域预测方法的评估
Bioinformatics. 2001 Jul;17(7):646-53. doi: 10.1093/bioinformatics/17.7.646.
10
Luciferase, when fused to an N-terminal signal peptide, is secreted from transfected Plasmodium falciparum and transported to the cytosol of infected erythrocytes.荧光素酶与N端信号肽融合后,可从转染的恶性疟原虫中分泌出来,并转运至被感染红细胞的细胞质中。
J Biol Chem. 2001 Jul 20;276(29):26838-45. doi: 10.1074/jbc.M100111200. Epub 2001 May 25.