| Literature DB >> 25489076 |
Eva Maria Novoa1, Noelia Camacho1, Anna Tor1, Barrie Wilkinson2, Steven Moss2, Patricia Marín-García3, Isabel G Azcárate4, José M Bautista4, Adam C Mirando5, Christopher S Francklyn5, Sònia Varon6, Miriam Royo7, Alfred Cortés8, Lluís Ribas de Pouplana9.
Abstract
Malaria remains a major global health problem. Emerging resistance to existing antimalarial drugs drives the search for new antimalarials, and protein translation is a promising pathway to target. Here we explore the potential of the aminoacyl-tRNA synthetase (ARS) family as a source of antimalarial drug targets. First, a battery of known and novel ARS inhibitors was tested against Plasmodium falciparum cultures, and their activities were compared. Borrelidin, a natural inhibitor of threonyl-tRNA synthetase (ThrRS), stands out for its potent antimalarial effect. However, it also inhibits human ThrRS and is highly toxic to human cells. To circumvent this problem, we tested a library of bioengineered and semisynthetic borrelidin analogs for their antimalarial activity and toxicity. We found that some analogs effectively lose their toxicity against human cells while retaining a potent antiparasitic activity both in vitro and in vivo and cleared malaria from Plasmodium yoelii-infected mice, resulting in 100% mice survival rates. Our work identifies borrelidin analogs as potent, selective, and unexplored scaffolds that efficiently clear malaria both in vitro and in vivo.Entities:
Keywords: aminoacyl-tRNA synthetase; borrelidin; drug design; malaria; plasmodium
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Year: 2014 PMID: 25489076 PMCID: PMC4280603 DOI: 10.1073/pnas.1405994111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205