| Literature DB >> 33691122 |
Luciana S Paradela1, Richard J Wall1, Sandra Carvalho1, Giulia Chemi2, Victoriano Corpas-Lopez1, Eoin Moynihan1, Davide Bello1, Stephen Patterson1, Maria Lucia S Güther1, Alan H Fairlamb1, Michael A J Ferguson1, Fabio Zuccotto2, Julio Martin3, Ian H Gilbert2, Susan Wyllie4.
Abstract
Phenotypic screening identified a benzothiophene compound with activity against Leishmania donovani, the causative agent of visceral leishmaniasis. Using multiple orthogonal approaches, oxidosqualene cyclase (OSC), a key enzyme of sterol biosynthesis, was identified as the target of this racemic compound and its enantiomers. Whole genome sequencing and screening of a genome-wide overexpression library confirmed that OSC gene amplification is associated with resistance to compound 1. Introduction of an ectopic copy of the OSC gene into wild-type cells reduced susceptibility to these compounds confirming the role of this enzyme in resistance. Biochemical analyses demonstrated the accumulation of the substrate of OSC and depletion of its product in compound (S)-1-treated-promastigotes and cell-free membrane preparations, respectively. Thermal proteome profiling confirmed that compound (S)-1 binds directly to OSC. Finally, modeling and docking studies identified key interactions between compound (S)-1 and the LdOSC active site. Strategies to improve the potency for this promising anti-leishmanial are proposed.Entities:
Keywords: Leishmania donovani; drug discovery; drug target; lanosterol; mechanism of action; neglected tropical disease; oxidosqualene cyclase; visceral leishmaniasis
Year: 2021 PMID: 33691122 DOI: 10.1016/j.chembiol.2021.02.008
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116