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Content archived on 2024-06-25

Vitamin biosynthesis as a target for antimalarial therapy

Objective

Plasmodium falciparum causes severe malaria and about 2 million human deaths annually. The main obstacle to combat the disease is increasing resistance of the parasites to existing drugs and the lack of a protective vaccine. Therefore, it is imperative that new suitable drug targets in the parasite?s metabolism are identified, assessed and validated. The availability of the parasite's genome sequence offers an excellent tool to identify metabolic pathways potentially essential for parasite survival. Scrutinising the Plasmodium genomes revealed that they possess biosynthetic pathways for vitamins. Vitamins are organic compounds required in small amounts to ensure normal metabolic functions. Since they are not synthesized by humans, they need to be supplied via nutrients in trace amounts. The absence of vitamin biosynthesis in humans suggests that specific targeting of these parasite pathways with inhibitors is feasible and thus vitamin biosynthesis of Plasmodium might offer excellent potential for the development of novel chemotherapeutics against malaria with specific toxicity towards the parasites without affecting the host's metabolism. In the first instance we will focus on vitamin B6 biosynthesis, as this important nutrient is required as a co-factor for a wide variety of essential metabolic functions in protein and amino acid metabolism and also has been implicated in the defence against oxidative stress in other eukaryotes. Using reverse genetic approaches we will validate the suitability of two of the vitamin B6 synthesising enzymes Pdx1 and Pdx2 respectively, as drug targets. In addition, their precise biological functions and potential interactions with other cellular components will be analyzed. Further the biochemical, biophysical and structural features of both enzymes will be assessed in order to be able to rationally design specific inhibitors that interfere with the parasite's proteins activities and functions.

Fields of science (EuroSciVoc)

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Keywords

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Topic(s)

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Call for proposal

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FP6-2003-LIFESCIHEALTH-3
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Funding Scheme

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STREP - Specific Targeted Research Project

Coordinator

UNIVERSITÄTSKLINIKUM HEIDELBERG
EU contribution
No data
Total cost

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Participants (4)

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