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Discovery of the first Mycobacterium tuberculosis MabA (FabG1) inhibitors through a fragment-based screening.

par Faïon, Léo;Djaout, Kamel;Frita, Rosangela;Pintiala, Catalin;Cantrelle, Francois-Xavier;Moune, Martin;Vandeputte, Alexandre;Bourbiaux, Kevin;Piveteau, Catherine;Herledan, Adrien;Biela, Alexandre;Leroux, Florence;Kremer, Laurent;Blaise, Mickael;Tanina, Abdalkarim;Wintjens, René ;Hanoulle, Xavier;Déprez, Benoit;Willand, Nicolas;Baulard, Alain R;Flipo, Marion
Référence European journal of medicinal chemistry, 200, page (112440)
Publication Publié, 2020-05-01

Article révisé par les pairs

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Résumé :

Mycobacterium tuberculosis (M.tb), the etiologic agent of tuberculosis, remains the leading cause of death from a single infectious agent worldwide. The emergence of drug-resistant M.tb strains stresses the need for drugs acting on new targets. Mycolic acids are very long chain fatty acids playing an essential role in the architecture and permeability of the mycobacterial cell wall. Their biosynthesis involves two fatty acid synthase (FAS) systems. Among the four enzymes (MabA, HadAB/BC, InhA and KasA/B) of the FAS-II cycle, MabA (FabG1) remains the only one for which specific inhibitors have not been reported yet. The development of a new LC-MS/MS based enzymatic assay allowed the screening of a 1280 fragment-library and led to the discovery of the first small molecules that inhibit MabA activity. A fragment from the anthranilic acid series was optimized into more potent inhibitors and their binding to MabA was confirmed by 19F ligand-observed NMR experiments.