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交通堵塞:恶性疟原虫中的蛋白质运输

Traffic jams: protein transport in Plasmodium falciparum.

作者信息

van Dooren G G, Waller R F, Joiner K A, Roos D S, McFadden G I

机构信息

Plant Cell Biology Research Centre, School of Botany, University of Melbourne, VIC 3010, Australia.

出版信息

Parasitol Today. 2000 Oct;16(10):421-7. doi: 10.1016/s0169-4758(00)01792-0.

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.

摘要

疟原虫中的蛋白质靶向是一个复杂的过程,涉及多个细胞区室,这些区室使这些细胞有别于酵母或哺乳动物等更为人熟知的系统。已知至少有十二个不同的蛋白质目的地。其中研究得最透彻的是残留叶绿体(顶质体),但新工具有望在理解恶性疟原虫及相关顶复门寄生虫如何将蛋白质运输到其与入侵相关的细胞器,以及它们如何通过将蛋白质运输到宿主细胞质和质膜中来修饰宿主方面取得快速进展。在此,吉尔·范·多伦及其同事讨论了对这个迷人且重要的系统中通过分泌途径进行蛋白质靶向的最新见解。这个主题在2000年澳大利亚洛恩举行的疟疾分子研究方法会议上成为一个主要议题。

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