Publications des scientifiques de l'IRD

Cassagnes L. E., Rakotoarivelo N., Sirigu S., Perio Pierre, Najahi E., Chavas L. M. G., Thompson A., Gayon R., Ferry G., Boutin J. A., Valentin A., Reybier K., Nepveu F. (2017). Role of quinone reductase 2 in the antimalarial properties of indolone-type derivatives. Molecules, 22 (2), p. art. 210 [16 p.]. ISSN 1420-3049.

Titre du document
Role of quinone reductase 2 in the antimalarial properties of indolone-type derivatives
Année de publication
2017
Type de document
Article référencé dans le Web of Science WOS:000395552400024
Auteurs
Cassagnes L. E., Rakotoarivelo N., Sirigu S., Perio Pierre, Najahi E., Chavas L. M. G., Thompson A., Gayon R., Ferry G., Boutin J. A., Valentin A., Reybier K., Nepveu F.
Source
Molecules, 2017, 22 (2), p. art. 210 [16 p.] ISSN 1420-3049
Indolone-N-oxides have antiplasmodial properties against Plasmodium falciparum at the erythrocytic stage, with IC50 values in the nanomolar range. The mechanism of action of indolone derivatives involves the production of free radicals, which follows their bioreduction by an unknown mechanism. In this study, we hypothesized that human quinone reductase 2 (hQR2), known to act as a flavin redox switch upon binding to the broadly used antimalarial chloroquine, could be involved in the activity of the redox-active indolone derivatives. Therefore, we investigated the role of hQR2 in the reduction of indolone derivatives. We analyzed the interaction between hQR2 and several indolone-type derivatives by examining enzymatic kinetics, the substrate/protein complex structure with X-ray diffraction analysis, and the production of free radicals with electron paramagnetic resonance. The reduction of each compound in cells overexpressing hQR2 was compared to its reduction in naive cells. This process could be inhibited by the specific hQR2 inhibitor, S29434. These results confirmed that the anti-malarial activity of indolone-type derivatives was linked to their ability to serve as hQR2 substrates and not as hQR2 inhibitors as reported for chloroquine, leading to the possibility that substrate of hQR2 could be considered as a new avenue for the design of new antimalarial compounds.
Plan de classement
Sciences fondamentales / Techniques d'analyse et de recherche [020] ; Entomologie médicale / Parasitologie / Virologie [052]
Localisation
Fonds IRD [F B010069389]
Identifiant IRD
fdi:010069389
Contact