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弓形虫移动连接复合体的鉴定:不同分泌细胞器之间的协作

Identification of the moving junction complex of Toxoplasma gondii: a collaboration between distinct secretory organelles.

作者信息

Alexander David L, Mital Jeffrey, Ward Gary E, Bradley Peter, Boothroyd John C

机构信息

Department of Microbiology and Immunology, Stanford University, Stanford, California, USA.

出版信息

PLoS Pathog. 2005 Oct;1(2):e17. doi: 10.1371/journal.ppat.0010017. Epub 2005 Oct 21.

Abstract

Apicomplexan parasites, including Toxoplasma gondii and Plasmodium sp., are obligate intracellular protozoa. They enter into a host cell by attaching to and then creating an invagination in the host cell plasma membrane. Contact between parasite and host plasma membranes occurs in the form of a ring-shaped moving junction that begins at the anterior end of the parasite and then migrates posteriorly. The resulting invagination of host plasma membrane creates a parasitophorous vacuole that completely envelops the now intracellular parasite. At the start of this process, apical membrane antigen 1 (AMA1) is released onto the parasite surface from specialized secretory organelles called micronemes. The T. gondii version of this protein, TgAMA1, has been shown to be essential for invasion but its exact role has not previously been determined. We identify here a trio of proteins that associate with TgAMA1, at least one of which associates with TgAMA1 at the moving junction. Surprisingly, these new proteins derive not from micronemes, but from the anterior secretory organelles known as rhoptries and specifically, for at least two, from the neck portion of these club-shaped structures. Homologues for these AMA1-associated proteins are found throughout the Apicomplexa strongly suggesting that this moving junction apparatus is a conserved feature of this important class of parasites. Differences between the contributing proteins in different species may, in part, be the result of selective pressure from the different niches occupied by these parasites.

摘要

顶复门寄生虫,包括刚地弓形虫和疟原虫属,是专性细胞内原生动物。它们通过附着于宿主细胞质膜并在其上形成内陷来进入宿主细胞。寄生虫与宿主质膜之间的接触以环形移动连接的形式发生,该连接始于寄生虫的前端,然后向后迁移。宿主质膜的内陷形成了一个吞噬泡,它完全包裹住了现在位于细胞内的寄生虫。在这个过程开始时,顶膜抗原1(AMA1)从称为微线体的特殊分泌细胞器释放到寄生虫表面。这种蛋白质的弓形虫版本TgAMA1已被证明对入侵至关重要,但其确切作用此前尚未确定。我们在此鉴定出一组与TgAMA1相关的蛋白质,其中至少有一种在移动连接处与TgAMA1相关。令人惊讶的是,这些新蛋白质并非来自微线体,而是来自称为棒状体的前部分泌细胞器,具体而言,至少有两种来自这些棒状结构的颈部。在整个顶复门中都发现了这些与AMA1相关蛋白质的同源物,这强烈表明这种移动连接装置是这类重要寄生虫的一个保守特征。不同物种中这些贡献蛋白质之间的差异可能部分是这些寄生虫所占据的不同生态位产生的选择压力的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f577/1266307/d3ad022a9768/ppat.0010017.g001.jpg

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