| Literature DB >> 25453091 |
María Belén Jiménez-Díaz1, Daniel Ebert2, Yandira Salinas3, Anupam Pradhan4, Adele M Lehane5, Marie-Eve Myrand-Lapierre6, Kathleen G O'Loughlin7, David M Shackleford8, Mariana Justino de Almeida9, Angela K Carrillo3, Julie A Clark3, Adelaide S M Dennis5, Jonathon Diep2, Xiaoyan Deng6, Sandra Duffy10, Aaron N Endsley7, Greg Fedewa2, W Armand Guiguemde3, María G Gómez1, Gloria Holbrook3, Jeremy Horst2, Charles C Kim11, Jian Liu12, Marcus C S Lee9, Amy Matheny3, María Santos Martínez1, Gregory Miller3, Ane Rodríguez-Alejandre1, Laura Sanz1, Martina Sigal3, Natalie J Spillman5, Philip D Stein12, Zheng Wang12, Fangyi Zhu3, David Waterson13, Spencer Knapp12, Anang Shelat3, Vicky M Avery10, David A Fidock9, Francisco-Javier Gamo1, Susan A Charman8, Jon C Mirsalis7, Hongshen Ma6, Santiago Ferrer1, Kiaran Kirk5, Iñigo Angulo-Barturen1, Dennis E Kyle4, Joseph L DeRisi2, David M Floyd12, R Kiplin Guy14.
Abstract
Drug discovery for malaria has been transformed in the last 5 years by the discovery of many new lead compounds identified by phenotypic screening. The process of developing these compounds as drug leads and studying the cellular responses they induce is revealing new targets that regulate key processes in the Plasmodium parasites that cause malaria. We disclose herein that the clinical candidate (+)-SJ733 acts upon one of these targets, ATP4. ATP4 is thought to be a cation-transporting ATPase responsible for maintaining low intracellular Na(+) levels in the parasite. Treatment of parasitized erythrocytes with (+)-SJ733 in vitro caused a rapid perturbation of Na(+) homeostasis in the parasite. This perturbation was followed by profound physical changes in the infected cells, including increased membrane rigidity and externalization of phosphatidylserine, consistent with eryptosis (erythrocyte suicide) or senescence. These changes are proposed to underpin the rapid (+)-SJ733-induced clearance of parasites seen in vivo. Plasmodium falciparum ATPase 4 (pfatp4) mutations that confer resistance to (+)-SJ733 carry a high fitness cost. The speed with which (+)-SJ733 kills parasites and the high fitness cost associated with resistance-conferring mutations appear to slow and suppress the selection of highly drug-resistant mutants in vivo. Together, our data suggest that inhibitors of PfATP4 have highly attractive features for fast-acting antimalarials to be used in the global eradication campaign.Entities:
Keywords: PfATP4; drug discovery; malaria
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Year: 2014 PMID: 25453091 PMCID: PMC4273362 DOI: 10.1073/pnas.1414221111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205