Identification and characterisation of high affinity nucleoside and nucleobase transporters in Toxoplasma gondii

被引:57
作者
De Koning, HP [1 ]
Al-Salabi, MI [1 ]
Cohen, AM [1 ]
Coombs, GH [1 ]
Wastling, JM [1 ]
机构
[1] Univ Glasgow, Inst Biomed & Life Sci, Div Infect & Immun, Glasgow G12 8QQ, Lanark, Scotland
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Toxoplasma gondii; purine salvage; nucleobase transporter; nucleoside transporter; pyrimidine uptake; apicomplexan;
D O I
10.1016/S0020-7519(03)00091-2
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 protozoan parasite Toxoplasma gondii depends upon salvaging the purines that it requires. We have re-analysed purine transport in T gondii and identified novel nucleoside and nucleobase transporters. The latter transports hypoxanthine (TgNBT1; K-m = 0.91 +/- 0.19 muM) and is inhibited by guanine and xanthine: it is the first high affinity nucleobase transporter to be identified in an apicomplexan parasite. The previously reported nucleoside transporter, TgAT1, is low affinity with K-m values of 105 and 134 muM for adenosine and mosine, respectively. We have now identified a second nucleoside transporter, TgAT2, which is high affinity and inhibited by adenosine, mosine, guanosine, uridine and thymidine (K-m values 0.28 +/- 1.5 muM) as well as cytidine (K-i = 32 muM). TgAT2 also recognises several nucleoside analogues with therapeutic potential. We have investigated the basis for the broad specificity of TgAT2 and found that hydrogen bonds are formed with the 3' and 5' hydroxyl groups and that the base groups are bound through H-bonds with either N3 of the purine ring or N(3)H of the pyrimidine ring, and most probably pi-pi-stacking as well. The identification of these high affinity purine nucleobase and nucleoside transporters reconciles for the first time the low abundance of free nucleosides and nucleobases in the intracellular environment with the efficient purine salvage carried out by T gondii. (C) 2003 Australian Society for Parasitology Inc. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:821 / 831
页数:11
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