Transport proteins of Plasmodium falciparum:: defining the limits of metabolism

被引:14
作者
Krishna, S [1 ]
Webb, R [1 ]
Woodrow, C [1 ]
机构
[1] Univ London St Georges Hosp, Sch Med, Sch Med, Dept Infect Dis, London SW17 0RE, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
Plasmodium falciparum; Xenopusoocyte; malaria infected erythrocyte; parasite plasma membrane; 'P'-type ATPase; hexose transporter;
D O I
10.1016/S0020-7519(01)00254-5
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
In this review we give an account of transport processes occurring at the membrane interface that separates the asexual stage of Plasmodium falciparum from its host, the infected erythrocyte, and also describe proteins whose activities may be important at this location. We explain the potential clinical value of such studies in the light of the current spread of parasite resistance to conventional antimalarial strategies. We discuss the uptake of substrates critical to the survival of the intracellular malaria parasite, and also the parasite's homeostatic and disposal mechanisms. The use of the Xenopus laevis expression system in the characterisation of a hexose transporter ('PfHT1') and a Ca2+ ATPase ('PfATP4') of the parasite plasma membrane are described in detail. (C) 2001 Australian Society for Parasitology Inc. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1331 / 1342
页数:12
相关论文
共 75 条
[31]   ENHANCED CHOLINE AND RB+ TRANSPORT IN HUMAN ERYTHROCYTES INFECTED WITH THE MALARIA PARASITE PLASMODIUM-FALCIPARUM [J].
KIRK, K ;
WONG, HY ;
ELFORD, BC ;
NEWBOLD, CI ;
ELLORY, JC .
BIOCHEMICAL JOURNAL, 1991, 278 :521-525
[32]   Membrane transport in the malaria-infected erythrocyte [J].
Kirk, K .
PHYSIOLOGICAL REVIEWS, 2001, 81 (02) :495-537
[33]  
KIRK K, 1994, J BIOL CHEM, V269, P3339
[34]   Glucose uptake in Plasmodium falciparum-infected erythrocytes is an equilibrative not an active process [J].
Kirk, K ;
Horner, HA ;
Kirk, J .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1996, 82 (02) :195-205
[35]   THE INCREASED K+ LEAK OF MALARIA-INFECTED ERYTHROCYTES IS NOT VIA A CA2+-ACTIVATED K+ CHANNEL [J].
KIRK, K ;
ELFORD, BC ;
ELLORY, JC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1135 (01) :8-12
[36]  
KIRK K, 1999, TRANSPORT TRAFFICKIN, P293
[37]  
KOZAK M, 1989, J CELL BIOL, V108, P229, DOI DOI 10.1083/JCB.108.2.229
[38]   Hexose transport in asexual stages of Plasmodium falciparum and kinetoplastidae [J].
Krishna, S ;
Woodrow, CJ ;
Burchmore, RJS ;
Saliba, KJ ;
Kirk, K .
PARASITOLOGY TODAY, 2000, 16 (12) :516-521
[39]   LACTIC-ACIDOSIS AND HYPOGLYCEMIA IN CHILDREN WITH SEVERE MALARIA - PATHOPHYSIOLOGICAL AND PROGNOSTIC-SIGNIFICANCE [J].
KRISHNA, S ;
WALLER, DW ;
TERKUILE, F ;
KWIATKOWSKI, D ;
CRAWLEY, J ;
CRADDOCK, CFC ;
NOSTEN, F ;
CHAPMAN, D ;
BREWSTER, D ;
HOLLOWAY, PA ;
WHITE, NJ .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1994, 88 (01) :67-73
[40]  
Krishna S, 1999, Novartis Found Symp, V226, P126