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Título: | High-affinity binding of silybin derivatives to the nucleotide-binding domain of a Leishmania tropica P-glycoprotein-like transporter and chemosensitization of a multidrug-resistant parasite to daunomycin |
Autor: | Pérez-Victoria, J. M. ; Pérez-Victoria, F. J.; Conseil, G.; Maitrejean, M.; Barron, D.; Castanys, Santiago; Gamarro, Francisco; Di Pietro, A.; Comte, Gilles | Fecha de publicación: | 2001 | Editor: | American Society for Microbiology | Citación: | Antimicrobial Agents and Chemotherapy 45: 439- 446 (2001) | Resumen: | In order to overcome the multidrug resistance mediated by P-glycoprotein-like transporters in Leishmania spp., we have studied the effects produced by derivatives of the flavanolignan silybin and related compounds lacking the monolignol unit on (i) the affinity of binding to a recombinant C-terminal nucleotide-binding domain of the L. tropica P-glycoprotein-like transporter and (ii) the sensitization to daunomycin on promastigote forms of a multidrug-resistant L. tropica line overexpressing the transporter. Oxidation of the flavanonol silybin to the corresponding flavonol dehydrosilybin, the presence of the monolignol unit, and the addition of a hydrophobic substituent such as dimethylallyl, especially at position 8 of ring A, considerably increased the binding affinity. The in vitro binding affinity of these compounds for the recombinant cytosolic domain correlated with their modulation of drug resistance phenotype. In particular, 8-(3,3-dimethylallyl)-dehydrosilybin effectively sensitized multidrug-resistant Leishmania spp. to daunomycin. The cytosolic domains are therefore attractive targets for the rational design of inhibitors against P-glycoprotein-like transporters. | URI: | http://hdl.handle.net/10261/81265 | DOI: | 10.1128/AAC.45.2.439-446.2001 | Identificadores: | doi: 10.1128/AAC.45.2.439-446.2001 issn: 0066-4804 |
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