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Kinetic modelling of phospholipid synthesis in Plasmodium knowlesi unravels crucial steps and relative importance of multiple pathways

机译:诺氏疟原虫中磷脂合成的动力学模型揭示了关键步骤和多种途径的相对重要性

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摘要

BackgroundPlasmodium is the causal parasite of malaria, infectious disease responsible for the death of up to one million people each year. Glycerophospholipid and consequently membrane biosynthesis are essential for the survival of the parasite and are targeted by a new class of antimalarial drugs developed in our lab. In order to understand the highly redundant phospholipid synthethic pathways and eventual mechanism of resistance to various drugs, an organism specific kinetic model of these metabolic pathways need to be developed in Plasmodium species.
机译:背景疟原虫是疟疾的致病性寄生虫,这种传染病每年导致多达100万人死亡。甘油磷脂和因此的膜生物合成对于寄生虫的生存是必不可少的,并且是我们实验室开发的新型抗疟疾药物的目标。为了了解高度冗余的磷脂合成途径和对多种药物的耐药性最终机制,需要在疟原虫物种中开发这些代谢途径的生物特异性动力学模型。

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