malarial parasite Plasmodium falciparum imports the human protein peroxiredoxin 2 for peroxide detoxification

Coevolution of the malarial parasite and its human host has resulted in a complex network of interactions contributing to the homeodynamics of the host-parasite unit. As a rapidly growing and multiplying organism, Plasmodium falciparum depends on an adequate antioxidant defense system that is effici...

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Veröffentlicht in:	Proceedings of the National Academy of Sciences - PNAS 2009-08, Vol.106 (32), p.13323-13328
Hauptverfasser:	Koncarevic, Sasa, Rohrbach, Petra, Deponte, Marcel, Krohne, Georg, Prieto, Judith Helena, Yates, John III, Rahlfs, Stefan, Becker, Katja
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Antibodies Biological Sciences Carrier Proteins - metabolism Cell Extracts Chloroquine - pharmacology Cytosol Cytosol - drug effects Cytosol - ultrastructure Enzyme kinetics Erythrocytes Erythrocytes - cytology Erythrocytes - drug effects Erythrocytes - parasitology Erythrocytes - ultrastructure Fluorescent Antibody Technique Green Fluorescent Proteins - metabolism Hemoglobins - metabolism Humans Imports Inactivation, Metabolic Kinetics Malaria Malaria, Falciparum - parasitology Membrane Proteins - metabolism Parasite hosts Parasites Parasitic protozoa Parasitism Peroxides - metabolism Peroxiredoxins - metabolism Peroxiredoxins - ultrastructure Plasmodium falciparum Plasmodium falciparum - cytology Plasmodium falciparum - drug effects Plasmodium falciparum - metabolism Plasmodium falciparum - ultrastructure Protein Transport - drug effects Proteins Protozoan Proteins - metabolism Thioredoxin Trophozoites Vacuoles - drug effects Vacuoles - metabolism Vacuoles - ultrastructure
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