Chemical Biology & Drug Design · 2011 · 11 citations · 29 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryMolecular PharmacologyEnzyme InhibitionLigand BindingLigand-based DesignIntermolecular Protein InteractionsProtective Antigen IdentificationProtein-protein Interaction Inhibitor DesignProtein-protein Interaction Inhibitor DiscoveryToxin Assembly
Two molecular scaffolds were designed using the CAVEAT molecular design package to inhibit the oligomerization of protective antigen (PA(63) ), a key protein component of anthrax toxin. The inhibitors were designed to prevent heptamerization of PA(63) by mimicking key residues of PA(63) needed for the intermolecular interactions that stabilize the heptamer. Using the scaffolds identified by CAVEAT, seven candidate inhibitors were synthesized and tested for their ability to inhibit anthrax toxin-induced cytotoxicity, with three of the agents demonstrating modest inhibition in murine J774A.1 macrophage cells.
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Identification of the cellular receptor for anthrax toxin
Kenneth A. Bradley, Jeremy Mogridge, Michaël Mourez et al. · Nature · 2001 · 845 citations
Crystal structure of the anthrax toxin protective antigen
Carlo Petosa, R. John Collier, Kurt R. Klimpel et al. · Nature · 1997 · 755 citations
Life Sciences, Biochemistry, Biology +14