PfCG2, a Plasmodium falciparum protein peripherally associated with the parasitophorous vacuolar membrane, is expressed in the period of maximum hemoglobin uptake and digestion by trophozoites

被引:11
|
作者
Cooper, RA
Papakrivos, J
Lane, KD
Fujioka, H
Lingelbach, K
Wellems, TE
机构
[1] NIAID, Lab Malaria & Vector Res, NIH, Bethesda, MD 20892 USA
[2] Univ Marburg, Fachbereich Biol Zool, D-35032 Marburg, Germany
[3] Old Dominion Univ, Dept Biol Sci, Norfolk, VA 23529 USA
[4] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
关键词
malaria; endocytosis; phagocytosis; protein trafficking; proteases;
D O I
10.1016/j.molbiopara.2005.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A Plasmodium falciparum gene closely linked to the chloroquine resistance locus encodes PfCG2, a predicted 320-330 kDa protein. In the parasitized erythrocyte, PfCG2 expression rises sharply in the trophozoite stage and is detected in electron-dense patches along the parasitophorous vacuolar membrane (PVM), in the cytoplasm and in the digestive vacuole (DV). Results of extraction and partitioning experiments show that PfCG2 is a peripheral membrane protein. Exposure of trophozoite-infected erythrocytes to trypsin-containing buffer after streptolysin O. permeabilization indicates that PfCG2 is exposed to the erythrocyte cytosol at the outer face of the PVM. PfCG2 is highly susceptible to hydrolysis by aspartic and cysteine proteases and shows dose-dependent accumulation in the presence of protease inhibitors. These results suggest that PfCG2 is delivered from the outside face of the PVM to the DV, where it is broken down by parasite proteases. PfCG2 interacts with erythrocyte cytoplasm and may be associated with processes of hemoglobin uptake and digestion by erythrocytic-stage parasites. Published by Elsevier B.V.
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页码:167 / 176
页数:10
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