Proteomics of the human malaria parasite Plasmodium falciparum

被引:23
|
作者
Sims, Paul F. G. [1 ]
Hyde, John E. [1 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M60 1QD, Lancs, England
基金
英国惠康基金;
关键词
cell cycle; drug challenge; mass spectrometry; metabolic labeling; post-translational modifications; quantitative proteomics; subproteome analysis;
D O I
10.1586/14789450.3.1.87
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The lethal species of malaria parasite, Plasmodium falciparum, continues to exact a huge toll of mortality and morbidity, particularly in sub-Saharan Africa. Completion of the genome sequence of this organism and advances in proteomics and mass spectrometry have opened up unprecedented opportunities for understanding the complex biology of this parasite and how it responds to drug challenge and other interventions. This review describes recent progress that has been made in applying proteomics technology to this important pathogen and provides a look forward to likely future developments.
引用
收藏
页码:87 / 95
页数:9
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