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蛋白质向疟原虫顶端细胞器的运输——构建入侵机制。

Protein trafficking to apical organelles of malaria parasites - building an invasion machine.

作者信息

Kats Lev M, Cooke Brian M, Coppel Ross L, Black Casilda G

机构信息

NHMRC Program in Malaria, Department of Microbiology, Monash University, Victoria 3800, Australia.

出版信息

Traffic. 2008 Feb;9(2):176-86. doi: 10.1111/j.1600-0854.2007.00681.x. Epub 2007 Dec 18.

Abstract

Malaria is caused by four species of apicomplexan protozoa belonging to the genus Plasmodium. These parasites possess a specialized collection of secretory organelles called rhoptries, micronemes and dense granules (DGs) that in part facilitate invasion of host cells. The mechanism by which the parasite traffics proteins to these organelles as well as regulates their secretion has important implications for understanding the invasion process and may lead to development of novel intervention strategies. In this review, we focus on emerging data about trafficking signals, mechanisms of biogenesis and secretion. At least some of these are conserved in higher eukaryotes, suggesting that rhoptries, micronemes and DGs are related to organelles such as secretory lysosomes that are well known to mainstream cell biologists.

摘要

疟疾由疟原虫属的四种顶复门原生动物引起。这些寄生虫拥有一组特殊的分泌细胞器,称为棒状体、微线体和致密颗粒(DGs),它们在一定程度上有助于侵入宿主细胞。寄生虫将蛋白质运输到这些细胞器以及调节其分泌的机制,对于理解入侵过程具有重要意义,并且可能会导致新的干预策略的开发。在这篇综述中,我们重点关注有关运输信号、生物发生和分泌机制的新数据。其中至少有一些在高等真核生物中是保守的,这表明棒状体、微线体和致密颗粒与主流细胞生物学家熟知的分泌性溶酶体等细胞器有关。

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