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疟原虫蛋白输出的新见解。

New insights into protein export in malaria parasites.

机构信息

Strategic Research Centre for Molecular and Medical Research, Deakin University, Waurn Ponds, Vic., Australia.

出版信息

Cell Microbiol. 2010 May 1;12(5):580-7. doi: 10.1111/j.1462-5822.2010.01455.x. Epub 2010 Feb 19.

Abstract

In order to survive and promote its virulence the malaria parasite must export hundreds of its proteins beyond an encasing vacuole and membrane into the host red blood cell. In the last few years, several major advances have been made that have significantly contributed to our understanding of this export process. These include: (i) the identification of sequences that direct protein export (a signal sequence and a motif termed PEXEL), which have allowed predictions of the exportomes of Plasmodium species that are the cause of malaria, (ii) the recognition that the fate of proteins destined for export is already decided within the parasite's endoplasmic reticulum and involves the PEXEL motif being recognized and cleaved by the aspartic protease plasmepsin V and (iii) the discovery of the Plasmodium translocon of exported proteins (PTEX) that is responsible for the passage of proteins across the vacuolar membrane. We review protein export in Plasmodium and these latest developments in the field that have now provided a new platform from which trafficking of malaria proteins can be dissected.

摘要

为了生存和增强其毒性,疟原虫必须将数百种蛋白质从包裹它们的液泡和膜中输出到宿主的红细胞内。在过去的几年中,取得了几项重大进展,极大地促进了我们对这一输出过程的理解。这些进展包括:(i)鉴定出指导蛋白质输出的序列(信号序列和一个称为 PEXEL 的基序),这使得能够预测引起疟疾的疟原虫物种的外显子组;(ii)认识到注定要输出的蛋白质的命运在寄生虫的内质网内就已经决定,涉及到 PEXEL 基序被天冬氨酸蛋白酶 plasmepsin V 识别和切割;(iii)发现了疟原虫输出蛋白的转运体(PTEX),它负责蛋白质穿过液泡膜的转运。我们综述了疟原虫中的蛋白质输出以及该领域的最新进展,这些进展为解析疟疾蛋白的运输提供了新的平台。

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