Literature DB >> 24325549

Membrane transport in the malaria parasite and its host erythrocyte.

Kiaran Kirk1, Adele M Lehane.   

Abstract

As it grows and replicates within the erythrocytes of its host the malaria parasite takes up nutrients from the extracellular medium, exports metabolites and maintains a tight control over its internal ionic composition. These functions are achieved via membrane transport proteins, integral membrane proteins that mediate the passage of solutes across the various membranes that separate the biochemical machinery of the parasite from the extracellular environment. Proteins of this type play a key role in antimalarial drug resistance, as well as being candidate drug targets in their own right. This review provides an overview of recent work on the membrane transport biology of the malaria parasite-infected erythrocyte, encompassing both the parasite-induced changes in the membrane transport properties of the host erythrocyte and the cell physiology of the intracellular parasite itself.

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Year:  2014        PMID: 24325549     DOI: 10.1042/BJ20131007

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  26 in total

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3.  Adaptation of Plasmodium falciparum to its transmission environment.

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Journal:  Nat Ecol Evol       Date:  2017-12-18       Impact factor: 15.460

4.  Plasmodium falciparum chloroquine resistance transporter is a H+-coupled polyspecific nutrient and drug exporter.

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Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-02       Impact factor: 11.205

5.  Salinomycin and other ionophores as a new class of antimalarial drugs with transmission-blocking activity.

Authors:  Sarah D'Alessandro; Yolanda Corbett; Denise P Ilboudo; Paola Misiano; Nisha Dahiya; Solomon M Abay; Annette Habluetzel; Romualdo Grande; Maria R Gismondo; Koen J Dechering; Karin M J Koolen; Robert W Sauerwein; Donatella Taramelli; Nicoletta Basilico; Silvia Parapini
Journal:  Antimicrob Agents Chemother       Date:  2015-06-08       Impact factor: 5.191

Review 6.  The malaria parasite cation ATPase PfATP4 and its role in the mechanism of action of a new arsenal of antimalarial drugs.

Authors:  Natalie Jane Spillman; Kiaran Kirk
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2015-08-27       Impact factor: 4.077

Review 7.  Host Delivery of Favorite Meals for Intracellular Pathogens.

Authors:  Yousef Abu Kwaik; Dirk Bumann
Journal:  PLoS Pathog       Date:  2015-06-25       Impact factor: 6.823

8.  Mutations in the P-type cation-transporter ATPase 4, PfATP4, mediate resistance to both aminopyrazole and spiroindolone antimalarials.

Authors:  Erika L Flannery; Case W McNamara; Sang Wan Kim; Tomoyo Sakata Kato; Fengwu Li; Christine H Teng; Kerstin Gagaring; Micah J Manary; Rachel Barboa; Stephan Meister; Kelli Kuhen; Joseph M Vinetz; Arnab K Chatterjee; Elizabeth A Winzeler
Journal:  ACS Chem Biol       Date:  2014-11-05       Impact factor: 5.100

9.  Targeting the Plasmodium vivax equilibrative nucleoside transporter 1 (PvENT1) for antimalarial drug development.

Authors:  Roman Deniskin; I J Frame; Yvett Sosa; Myles H Akabas
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2015-11-28       Impact factor: 4.077

10.  Na+ Influx Induced by New Antimalarials Causes Rapid Alterations in the Cholesterol Content and Morphology of Plasmodium falciparum.

Authors:  Sudipta Das; Suyash Bhatanagar; Joanne M Morrisey; Thomas M Daly; James M Burns; Isabelle Coppens; Akhil B Vaidya
Journal:  PLoS Pathog       Date:  2016-05-26       Impact factor: 6.823

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