Functional screening of selective mitochondrial inhibitors of Plasmodium

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 fut...

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Main Authors: Maria G. Gomez-Lorenzo, Ane Rodríguez-Alejandre, Sonia Moliner-Cubel, María Martínez-Hoyos, Noemí Bahamontes-Rosa, Rubén Gonzalez del Rio, Carolina Ródenas, Jesús de la Fuente, Jose Luis Lavandera, Jose F. García-Bustos, Alfonso Mendoza-Losana
Format: Article
Language:English
Published: Elsevier 2018-08-01
Series:International Journal for Parasitology: Drugs and Drug Resistance
Online Access:http://www.sciencedirect.com/science/article/pii/S2211320717301203
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spelling doaj-d31fe5e392d8459fb92b14da48cc417a2020-11-24T22:30:21ZengElsevierInternational Journal for Parasitology: Drugs and Drug Resistance2211-32072018-08-0182295303Functional screening of selective mitochondrial inhibitors of PlasmodiumMaria G. Gomez-Lorenzo0Ane Rodríguez-Alejandre1Sonia Moliner-Cubel2María Martínez-Hoyos3Noemí Bahamontes-Rosa4Rubén Gonzalez del Rio5Carolina Ródenas6Jesús de la Fuente7Jose Luis Lavandera8Jose F. García-Bustos9Alfonso Mendoza-Losana10Diseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, SpainCentro de Investigación Básica (CIB) GlaxoSmithKline, Tres Cantos, Madrid, SpainCentro de Investigación Básica (CIB) GlaxoSmithKline, Tres Cantos, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, Spain; Department of Basic Medical Science, CEU San Pablo University, Julián Romea 23, 28003, Madrid, SpainDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, Spain; Department of Microbiology and Biomedicine Discovery Institute, Monash University, 3800, VIC, AustraliaDiseases of the Developing World (DDW), Tres Cantos Medicine Development Campus, GlaxoSmithKline, Severo Ochoa 2, 28760, Tres Cantos, Madrid, Spain; Corresponding author. C/ Severo Ochoa, 2, Tres Cantos, 28760, Madrid, Spain.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: Plasmodium falciparum, Plasmodium yoelii, Oxygen consumption, Mitochondrial inhibitors and cytochromehttp://www.sciencedirect.com/science/article/pii/S2211320717301203
collection DOAJ
language English
format Article
sources DOAJ
author Maria G. Gomez-Lorenzo
Ane Rodríguez-Alejandre
Sonia Moliner-Cubel
María Martínez-Hoyos
Noemí Bahamontes-Rosa
Rubén Gonzalez del Rio
Carolina Ródenas
Jesús de la Fuente
Jose Luis Lavandera
Jose F. García-Bustos
Alfonso Mendoza-Losana
spellingShingle Maria G. Gomez-Lorenzo
Ane Rodríguez-Alejandre
Sonia Moliner-Cubel
María Martínez-Hoyos
Noemí Bahamontes-Rosa
Rubén Gonzalez del Rio
Carolina Ródenas
Jesús de la Fuente
Jose Luis Lavandera
Jose F. García-Bustos
Alfonso Mendoza-Losana
Functional screening of selective mitochondrial inhibitors of Plasmodium
International Journal for Parasitology: Drugs and Drug Resistance
author_facet Maria G. Gomez-Lorenzo
Ane Rodríguez-Alejandre
Sonia Moliner-Cubel
María Martínez-Hoyos
Noemí Bahamontes-Rosa
Rubén Gonzalez del Rio
Carolina Ródenas
Jesús de la Fuente
Jose Luis Lavandera
Jose F. García-Bustos
Alfonso Mendoza-Losana
author_sort Maria G. Gomez-Lorenzo
title Functional screening of selective mitochondrial inhibitors of Plasmodium
title_short Functional screening of selective mitochondrial inhibitors of Plasmodium
title_full Functional screening of selective mitochondrial inhibitors of Plasmodium
title_fullStr Functional screening of selective mitochondrial inhibitors of Plasmodium
title_full_unstemmed Functional screening of selective mitochondrial inhibitors of Plasmodium
title_sort functional screening of selective mitochondrial inhibitors of plasmodium
publisher Elsevier
series International Journal for Parasitology: Drugs and Drug Resistance
issn 2211-3207
publishDate 2018-08-01
description 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: Plasmodium falciparum, Plasmodium yoelii, Oxygen consumption, Mitochondrial inhibitors and cytochrome
url http://www.sciencedirect.com/science/article/pii/S2211320717301203
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