Traffic Jams: Protein Transport in Plasmodium falciparum

G.G van Dooren , R.F Waller , G.I McFadden , K.A Joiner , D.S Roos
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引用次数: 58

Abstract

Protein targeting in malaria parasites is a complex process, involving several cellular compartments that distinguish these cells from more familiar systems, such as yeast or mammals. At least a dozen distinct protein destinations are known. The best studied of these is the vestigial chloroplast (the apicoplast), but new tools promise rapid progress in understanding how Plasmodium falciparum and related apicomplexan parasites traffic proteins to their invasion-related organelles, and how they modify the host by trafficking proteins into its cytoplasm and plasma membrane. Here, Giel van Dooren and colleagues discuss recent insights into protein targeting via the secretory pathway in this fascinating and important system. This topic emerged as a major theme at the Molecular Approaches to Malaria conference, Lorne, Australia, 2–5 February 2000.

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交通堵塞:恶性疟原虫的蛋白质运输
疟疾寄生虫的蛋白质靶向是一个复杂的过程,涉及到将这些细胞与更熟悉的系统(如酵母或哺乳动物)区分开来的几个细胞区室。至少有12种不同的蛋白质目的地是已知的。其中研究得最好的是退化叶绿体(顶质体),但新的工具有望在理解恶性疟原虫和相关的顶复合体寄生虫如何将蛋白质运输到其入侵相关细胞器,以及它们如何通过将蛋白质运输到其细胞质和质膜来修饰宿主方面取得快速进展。在这里,Giel van Dooren和他的同事讨论了在这个迷人而重要的系统中通过分泌途径靶向蛋白质的最新见解。在2000年2月2日至5日于澳大利亚洛恩举行的疟疾分子方法会议上,这一主题成为一个主要主题。
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Websites of interest Neosporosis. Seeking new targets for antiparasitic agents Response from A. Serero et al. Parasitology nomenclature – a recommendation Implications for neonatal HIV/AIDS and TB of sensitization in utero to helminths
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