A picomolar inhibitor of the Plasmodium falciparum IPP pathway

Author:

Kabeche Stephanie1ORCID,Braukmann Thomas2,Doenier Jon1,Meister Thomas3ORCID,Yeh Ellen245ORCID

Affiliation:

1. Department of Biochemistry, Stanford University School of Medicine, Stanford, California, USA

2. Department of Pathology, Stanford University School of Medicine, Stanford, California, USA

3. Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, California, USA

4. Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, California, USA

5. Chan Zuckerberg Biohub, San Francisco, California, USA

Abstract

ABSTRACT We identified MMV026468 as a picomolar inhibitor of blood-stage Plasmodium falciparum . Phenotyping assays, including isopentenyl diphosphate rescue of parasite growth inhibition, demonstrated that it targets MEP isoprenoid precursor biosynthesis. MMV026468-treated parasites showed an overall decrease in MEP pathway intermediates, which could result from inhibition of the first MEP enzyme DXS or steps prior to DXS such as regulation of the MEP pathway. Selection of MMV026468-resistant parasites lacking DXS mutations suggested that other targets are possible. The identification of MMV026468 could lead to a new class of antimalarial isoprenoid inhibitors.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Chan Zuckerberg Initiative

HHS | National Institutes of Health

Burroughs Wellcome Fund

Publisher

American Society for Microbiology

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