Functional screening of selective mitochondrial inhibitors of Plasmodium

Int J Parasitol Drugs Drug Resist. 2018 Aug;8(2):295-303. doi: 10.1016/j.ijpddr.2018.04.007. Epub 2018 May 9.

Abstract

Phenotypic screening has produced most of the new chemical entities currently in clinical development for malaria, plus many lead compounds active against Plasmodium falciparum asexual stages. However, lack of knowledge about the mode of action of these compounds delays and may even hamper their future development. Identifying the mode of action of the inhibitors greatly helps to prioritise compounds for further development as novel antimalarials. Here we describe a whole-cell method to detect inhibitors of the mitochondrial electron transport chain, using oxygen consumption as high throughput readout in 384-well plate format. The usefulness of the method has been confirmed with the Tres Cantos Antimalarial Compound Set (TCAMS). The assay identified 124 respiratory inhibitors in TCAMS, seven of which were novel anti-plasmodial chemical structures never before described as mitochondrial inhibitors.

Keywords: Mitochondrial inhibitors and cytochrome; Oxygen consumption; Plasmodium falciparum; Plasmodium yoelii.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimalarials / pharmacology*
  • Drug Discovery / methods
  • Drug Evaluation, Preclinical / instrumentation
  • Drug Evaluation, Preclinical / methods*
  • Electron Transport Chain Complex Proteins / antagonists & inhibitors
  • Humans
  • Inhibitory Concentration 50
  • Malaria / drug therapy
  • Malaria / parasitology
  • Malaria, Falciparum
  • Mitochondria / drug effects*
  • Oxygen / metabolism
  • Plasmodium falciparum / cytology
  • Plasmodium falciparum / drug effects*

Substances

  • Antimalarials
  • Electron Transport Chain Complex Proteins
  • Oxygen