Antimalarial drug discovery: targeting protein kinases

被引:62
作者
Doerig, Christian
Meijer, Laurent
机构
[1] Univ Glasgow, INSERM, U609, Wellcome Ctr Mol Parasitol,Biomed Res Ctr, Glasgow, Lanark, Scotland
[2] CNRS, Biol Stn, Cell Cycle Grp, F-29680 Roscoff, Bretagne, France
关键词
malaria; Plasmodium; protein kinase; selectivity; structure-based design; transmission-blocking;
D O I
10.1517/14728222.11.3.279
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein kinases (PKs) are prime targets for drug discovery in a variety of diseases, including cancer and neurodegenerative pathologies. The characterisation of the kinome of the human malaria parasite Plasmodium falciparum has revealed profound divergences, at several levels, between PKs of the parasite and those of its host. Here, the authors review the major issues and recent advances regarding the development of Plasmodium-selective PK inhibitors, with emphasis on target identification and validation, and on structure-based design. The authors also discuss the possibility of interfering with: i) Plasmodium PKs regulating transmission to the mosquito vector; and ii) host PKs that may be required for parasite survival.
引用
收藏
页码:279 / 290
页数:12
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