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Inhibitory interactions of the 2,3-dihydro-6,7-dihydroxy-1H-isoindol-1-one scaffold with Bunyavirales cap-snatching endonucleases expose relevant drug design features.
Miglioli, Francesca; Joel, Shindhuja; Tegoni, Matteo; Neira-Pelén, Pedro; Günther, Stephan; Carcelli, Mauro; Fisicaro, Emilia; Brancale, Andrea; Fernández-García, Yaiza; Rogolino, Dominga.
Afiliación
  • Miglioli F; Department of Chemistry, Life Sciences, Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124, Parma, Italy.
  • Joel S; Department of Virology, Bernhard-Nocht Institute for Tropical Medicine, Hamburg, Germany.
  • Tegoni M; Department of Chemistry, Life Sciences, Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124, Parma, Italy.
  • Neira-Pelén P; Department of Virology, Bernhard-Nocht Institute for Tropical Medicine, Hamburg, Germany.
  • Günther S; Department of Virology, Bernhard-Nocht Institute for Tropical Medicine, Hamburg, Germany.
  • Carcelli M; Department of Chemistry, Life Sciences, Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124, Parma, Italy.
  • Fisicaro E; Department of Food and Drug, University of Parma, Viale delle Scienze 27/A, 43124, Parma, Italy.
  • Brancale A; Department of Organic Chemistry, University of Chemistry and Technology, 16628, Prague, Czech Republic.
  • Fernández-García Y; Department of Virology, Bernhard-Nocht Institute for Tropical Medicine, Hamburg, Germany. Electronic address: fernandez-garcia@bnitm.de.
  • Rogolino D; Department of Chemistry, Life Sciences, Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124, Parma, Italy. Electronic address: dominga.rogolino@unipr.it.
Eur J Med Chem ; 272: 116467, 2024 Jun 05.
Article en En | MEDLINE | ID: mdl-38735150
ABSTRACT
The World Health Organization (WHO) identifies several bunyaviruses as significant threats to global public health security. Developing effective therapies against these viruses is crucial to combat future outbreaks and mitigate their impact on patient outcomes. Here, we report the synthesis of some isoindol-1-one derivatives and explore their inhibitory properties over an indispensable metal-dependent cap-snatching endonuclease (Cap-ENDO) shared among evolutionary divergent bunyaviruses. The compounds suppressed RNA hydrolysis by Cap-ENDOs, with IC50 values predominantly in the lower µM range. Molecular docking studies revealed the interactions with metal ions to be essential for the 2,3-dihydro-6,7-dihydroxy-1H-isoindol-1-one scaffold activity. Calorimetric analysis uncovered Mn2+ ions to have the highest affinity for sites within the targets, irrespective of aminoacidic variations influencing metal cofactor preferences. Interestingly, spectrophotometric findings unveiled sole dinuclear species formation between the scaffold and Mn2+. Moreover, the complexation of two Mn2+ ions within the viral enzymes appears to be favourable, as indicated by the binding of compound 11 to TOSV Cap-ENDO (Kd = 28 ± 3 µM). Additionally, the tendency of compound 11 to stabilize His+ more than His- Cap-ENDOs suggests exploitable differences in their catalytic pockets relevant to improving specificity. Collectively, our results underscore the isoindolinone scaffold's potential as a strategic starting point for the design of pan-antibunyavirus drugs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diseño de Fármacos / Endonucleasas / Simulación del Acoplamiento Molecular Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diseño de Fármacos / Endonucleasas / Simulación del Acoplamiento Molecular Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Francia