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Mechanism of antimalarial action of the synthetic trioxoane RBX11160 (OZ277)
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Uhlemann, Anne-Catrin
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机构: St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 0RE, England

Wittlin, Sergio
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机构: St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 0RE, England

Matile, Hugues
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机构: St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 0RE, England

Bustamante, Leyla Y.
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机构: St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 0RE, England

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机构:
[1] St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 0RE, England
[2] Swiss Trop Inst, CH-4002 Basel, Switzerland
[3] F Hoffmann La Roche & Cre AG, CH-4070 Basel, Switzerland
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D O I:
10.1128/AAC.01064-06
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
RBX11160 (OZ277) is a fully synthetic peroxidic antimalarial in clinical development. To study the possible mechanisms of action of RBX11160, we have examined its ability to inhibit PfATP6, a sarcoplasmic reticulum calcium ATPase and proposed target for semisynthetic peroxidic artemisinin derivatives. RBX11160 inhibits PfATP6 (apparent half-maximal inhibitory constant = 7,700 nM) less potently than artemisinin (79 nM). Inhibition of PfATP6 is abrogated by desferrioxamine, an iron-chelating agent. Consistent with this finding, the killing of Plasmodiuntfalciparum organisms by RBX11160 in vitro is antagonized by desferrioxamine. Artesunate and RBX11160 also act antagonistically against P. falciparum in vitro. A fluorescent derivative of RBX11160 localizes to the parasite cytosol in some parasites and to the food vacuole in other parasites. These data demonstrate that there are both similarities and differences between the antimalarial properties of RBX11160 and those of semisynthetic antimalarials such as artesunate and artemisinin.
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页码:667 / 672
页数:6
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