Comparative folate metabolism in humans and malaria parasites (part II):: activities as yet untargeted or specific to Plasmodium

被引:41
作者
Nzila, A
Ward, SA
Marsh, K
Sims, PFG
Hyde, JE
机构
[1] Wellcome Trust Res Labs, Kenya Med Res Inst, Nairobi 00100, Kenya
[2] Wellcome Trust Res Labs, Wellcome Trust Collaborat Res Program, Nairobi 00100, Kenya
[3] Univ Liverpool, Dept Pharmacol & Therapeut, Liverpool L69 3BX, Merseyside, England
[4] Univ Liverpool, Liverpool Sch Trop Med, Liverpool L53 QA, Merseyside, England
[5] Ctr Geog Med Res, Kenya Med Res Inst, Kilifi, Kenya
[6] Ctr Geog Med Res, Wellcome Trust Collaborat Res Program, Kilifi, Kenya
[7] John Radcliffe Hosp, Nuffield Dept Med, Oxford OX3 9DU, England
[8] Univ Manchester, Fac Life Sci, Manchester M60 1QD, Lancs, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.pt.2005.05.008
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The follate pathway represents a powerful target for combating rapidly dividing systems such as cancer cells, bacteria and malaria parasites. Whereas folate metabolism in mammalian cells and bacteria has been studied extensively, it is understood less well in malaria parasites. In two articles, we attempt to reconstitute the malaria folate pathway based on available information from mammalian and microbial systems, in addition to Plasmodium-genome-sequencing projects. In part 1, we focused on folate enzymes that are already used clinically as anticancer drug targets or that are under development in drug-discovery programs. In this article, we discuss mammalian folate enzymes that have not yet been exploited as potential drug targets, and enzymes that function in the de novo folate-synthesis pathway of the parasite - a particularly attractive area of attack because of its absence from the mammalian host.
引用
收藏
页码:334 / 339
页数:6
相关论文
共 41 条
[1]   Methenyltetrahydrofolate synthetase regulates folate turnover and accumulation [J].
Anguera, MC ;
Suh, JR ;
Ghandour, H ;
Nasrallah, IM ;
Selhub, J ;
Stover, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29856-29862
[2]   THE METHIONINE SYNTHESIS CYCLE AND SALVAGE OF METHYLTETRAHYDROFOLATE FROM HOST RED-CELLS IN THE MALARIA PARASITE (PLASMODIUM-FALCIPARUM) [J].
ASAWAMAHASAKDA, W ;
YUTHAVONG, Y .
PARASITOLOGY, 1993, 107 :1-10
[3]   Polymorphisms of methylenetetrahydrofolate reductase and other enzymes: Metabolic significance, risks and impact on folate requirement [J].
Bailey, LB ;
Gregory, JF .
JOURNAL OF NUTRITION, 1999, 129 (05) :919-922
[4]  
Barredo J, 1999, CANC DRUG DISC DEV, P323
[5]   The folic acid biosynthesis pathway in bacteria: evaluation of potential for antibacterial drug discovery [J].
Bermingham, A ;
Derrick, JP .
BIOESSAYS, 2002, 24 (07) :637-648
[6]   SEQUENCE VARIATION OF THE HYDROXYMETHYLDIHYDROPTERIN PYROPHOSPHOKINASE - DIHYDROPTEROATE SYNTHASE GENE IN-LINE SO THE HUMAN MALARIA PARASITE, PLASMODIUM-FALCIPARUM, WITH DIFFERING RESISTANCE TO SULFADOXINE [J].
BROOKS, DR ;
WANG, P ;
READ, M ;
WATKINS, WM ;
SIMS, PFG ;
HYDE, JE .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 224 (02) :397-405
[7]   The crystal structure of the hydrolase domain of 10-formyltetrahydrofolate dehydrogenase - Mechanism of hydrolysis and its interplay with the dehydrogenase domain [J].
Chumanevich, AA ;
Krupenko, SA ;
Davies, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (14) :14355-14364
[8]   ENZYMATIC CHARACTERIZATION OF BACILLUS-SUBTILIS GTP CYCLOHYDROLASE-I - EVIDENCE FOR A CHEMICAL DEPHOSPHORYLATION OF DIHYDRONEOPTERIN TRIPHOSPHATE [J].
DESAIZIEU, A ;
VANKAN, P ;
VANLOON, APGM .
BIOCHEMICAL JOURNAL, 1995, 306 :371-377
[9]   Syntheses of highly functionalised 6-substituted pteridines [J].
Guiney, D ;
Gibson, CL ;
Suckling, CJ .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (04) :664-675
[10]   SIMPLE RADIOASSAY FOR DIHYDROFOLATE SYNTHETASE-ACTIVITY IN ESCHERICHIA-COLI AND ITS APPLICATION TO AN INHIBITION STUDY OF NEW PTEROATE ANALOGS [J].
HO, RI ;
CORMAN, L ;
HO, J ;
NAIR, MG .
ANALYTICAL BIOCHEMISTRY, 1976, 73 (02) :493-500