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An Efficient Way to Screen Inhibitors of Energy-Coupling Factor (ECF) Transporters in a Bacterial Uptake Assay.
Bousis, Spyridon; Winkler, Steffen; Haupenthal, Jörg; Fulco, Francesco; Diamanti, Eleonora; Hirsch, Anna K H.
Afiliación
  • Bousis S; Helmholtz Centre for Infection Research (HZI), Helmholtz Institute for Pharmaceutical Research (HIPS), Campus Building E 8.1, D-66123 Saarbrücken, Germany.
  • Winkler S; Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 7, 9747 AG Groningen, The Netherlands.
  • Haupenthal J; Department of Pharmacy, Saarland University, Campus Building E8.1, 66123 Saarbrücken, Germany.
  • Fulco F; Helmholtz Centre for Infection Research (HZI), Helmholtz Institute for Pharmaceutical Research (HIPS), Campus Building E 8.1, D-66123 Saarbrücken, Germany.
  • Diamanti E; Helmholtz Centre for Infection Research (HZI), Helmholtz Institute for Pharmaceutical Research (HIPS), Campus Building E 8.1, D-66123 Saarbrücken, Germany.
  • Hirsch AKH; Helmholtz Centre for Infection Research (HZI), Helmholtz Institute for Pharmaceutical Research (HIPS), Campus Building E 8.1, D-66123 Saarbrücken, Germany.
Int J Mol Sci ; 23(5)2022 Feb 27.
Article en En | MEDLINE | ID: mdl-35269783
Herein, we report a novel whole-cell screening assay using Lactobacillus casei as a model microorganism to identify inhibitors of energy-coupling factor (ECF) transporters. This promising and underexplored target may have important pharmacological potential through modulation of vitamin homeostasis in bacteria and, importantly, it is absent in humans. The assay represents an alternative, cost-effective and fast solution to demonstrate the direct involvement of these membrane transporters in a native biological environment rather than using a low-throughput in vitro assay employing reconstituted proteins in a membrane bilayer system. Based on this new whole-cell screening approach, we demonstrated the optimization of a weak hit compound (2) into a small molecule (3) with improved in vitro and whole-cell activities. This study opens the possibility to quickly identify novel inhibitors of ECF transporters and optimize them based on structure-activity relationships.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Bacterias / Proteínas Bacterianas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Bacterias / Proteínas Bacterianas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2022 Tipo del documento: Article País de afiliación: Alemania