Charpian Stefan, Przyborski Jude M
Department of Parasitology, FB Biologie, Philipps University Marburg, Karl von Frisch Strasse 8, 35032 Marburg, Germany.
Traffic. 2008 Feb;9(2):157-65. doi: 10.1111/j.1600-0854.2007.00648.x. Epub 2007 Oct 17.
The human malaria parasite Plasmodium falciparum resides and multiplies within a membrane-bound vacuole in the cytosol of its host cell, the mature human erythrocyte. To enable the parasite to complete its intraerythrocytic life cycle, a large number of parasite proteins are synthesized and transported from the parasite to the infected cell. To gain access to the erythrocyte, parasite proteins must first cross the membrane of the parasitophorous vacuole (PVM), a process that is not well understood at the mechanistic level. Here, we review past and current literature on this topic, and make tentative predictions about the nature of the transport machinery required for transport of proteins across the PVM, and the molecular factors involved.
人类疟原虫恶性疟原虫寄生于其宿主细胞——成熟人类红细胞的胞质中一个膜结合的液泡内并在其中繁殖。为使疟原虫能够完成其在红细胞内的生命周期,大量疟原虫蛋白被合成并从疟原虫转运至被感染细胞。为进入红细胞,疟原虫蛋白必须首先穿过寄生泡膜(PVM),这一过程在机制层面上尚不清楚。在此,我们回顾关于该主题的过去和当前文献,并对蛋白质穿过PVM所需转运机制的性质以及所涉及的分子因素做出初步预测。