Transport processes in Plasmodium falciparum-infected erythrocytes:: potential as new drug targets

被引:24
作者
Krishna, S
Eckstein-Ludwig, U
Joët, T
Uhlemann, AC
Morin, C
Webb, R
Woodrow, C
Kun, JFJ
Kremsner, PG
机构
[1] St George Hosp, Sch Med, Dept Infect Dis, London SW17 0RE, England
[2] Lab Etudes Dynam & Struct Selectivite, F-38041 Grenoble 9, France
[3] Univ Tubingen, Inst Tropenmed, Sekt Humanparasitol, D-72074 Tubingen, Germany
关键词
Plasmodium; transporter; ATPase; channel; drug target;
D O I
10.1016/S0020-7519(02)00185-6
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Plasmodium falciparum infection induces alterations in the transport properties of infected erythrocytes that have recently been defined using electrophysiological techniques. Mechanisms responsible for transport of substrates into intraerythrocytic parasites have also been clarified by studies of three substrate-specific (hexose, nucleoside and aquaglyceroporin) parasite plasma membrane transporters. These have been characterised functionally using the Xenopus laevis oocyte heterologous expression system. The same expression system is currently being used to define the function of parasite 'P' type ATPases responsible for intraparasitic [Ca2+] homeostasis. We review studies on these transport processes and examine their potential as novel drug targets. (C) 2002 Published by Elsevier Science Ltd. on behalf of Australian Society for Parasitology Inc.
引用
收藏
页码:1567 / 1573
页数:7
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