Subtle changes in endochin-like quinolone (ELQ) structure alter site of inhibition within the cytochrome bc1 complex of Plasmodium falciparum

20 Jan 2015

Allison M. Stickles, Mariana Justino de Almeida, Joanne M. Morrisey, Kayla A.  Sheridan,  Isaac  P.  Forquer,  Aaron  Nilsen,  Rolf  W.  Winter,  Jeremy  N. Burrows, David A. Fidock, Akhil B. Vaidya, Michael K. Riscoe

Antimicrobial Agents and Chemotherapy


Photo: Pichit/


The cytochrome bc1 complex (cyt bc1) is the third component of the mitochondrial electron transport chain and is the target of several potent antimalarial compounds, including the naphthoquinone atovaquone (ATV) and the 4(1H)-quinolone ELQ-300. Mechanistically, cyt bc1 facilitates the transfer of electrons from ubiquinol to cytochrome c and contains both oxidative (Qo) and reductive (Qi) catalytic sites that are amenable to small molecule inhibition. Although many antimalarial compounds, including ATV, effectively target the Qo site, it has been challenging to design selective Qi site inhibitors with the ability to circumvent clinical ATV resistance, and little is known about how chemical structure contributes to site selectivity within cyt bc1. Here, we used the proposed Qi site inhibitor ELQ-300 to generate a drug-resistant P. falciparum clone containing an I22L mutation at the Qi region of cyt b. Using this "D1" clone and the Y268S Qo mutant strain, Tm90-C2B, we created a structure activity map of Qi vs. Qo site selectivity for a series of endochin-like, 4(1H)-quinolones (ELQs). We found that Qi site inhibition was associated with compounds containing 6-position halogens or aryl 3-position side chains, while Qo site inhibition was favored by 5,7-dihalogen groups or 7-position substituents. In addition to identifying ELQ-300 as a preferential Qi site inhibitor, our data suggest that the 4(1H)-quinolone scaffold is compatible with binding to either site of cyt bc1 and that minor chemical changes can influence Qo or Qi site inhibition by the ELQs.

View the full article on the Antimicrobial Agents and Chemotherapy website.