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Peptide-Alkoxyamine Drugs: An Innovative Approach to Fight Schistosomiasis: "Digging Their Graves with Their Forks".
Embo-Ibouanga, Ange W; Nguyen, Michel; Joly, Jean-Patrick; Coustets, Mathilde; Augereau, Jean-Michel; Paloque, Lucie; Vanthuyne, Nicolas; Bikanga, Raphaël; Robert, Anne; Benoit-Vical, Françoise; Audran, Gérard; Mellet, Philippe; Boissier, Jérôme; Marque, Sylvain R A.
Afiliación
  • Embo-Ibouanga AW; Aix-Marseille University, CNRS, UMR 7273, Case 551, Avenue Escadrille Normandie-Niemen, CEDEX 20, 13397 Marseille, France.
  • Nguyen M; Laboratoire de Chimie de Coordination (LCC-CNRS) and, New Antimalarial Molecules and Pharmacological Approaches (MAAP), Inserm ERL 1289, Université de Toulouse, CNRS, 31077 Toulouse, France.
  • Joly JP; Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III-Paul Sabatier (UPS), 31077 Toulouse, France.
  • Coustets M; Aix-Marseille University, CNRS, UMR 7273, Case 551, Avenue Escadrille Normandie-Niemen, CEDEX 20, 13397 Marseille, France.
  • Augereau JM; Laboratoire de Chimie de Coordination (LCC-CNRS) and, New Antimalarial Molecules and Pharmacological Approaches (MAAP), Inserm ERL 1289, Université de Toulouse, CNRS, 31077 Toulouse, France.
  • Paloque L; Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III-Paul Sabatier (UPS), 31077 Toulouse, France.
  • Vanthuyne N; Laboratoire de Chimie de Coordination (LCC-CNRS) and, New Antimalarial Molecules and Pharmacological Approaches (MAAP), Inserm ERL 1289, Université de Toulouse, CNRS, 31077 Toulouse, France.
  • Bikanga R; Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III-Paul Sabatier (UPS), 31077 Toulouse, France.
  • Robert A; Laboratoire de Chimie de Coordination (LCC-CNRS) and, New Antimalarial Molecules and Pharmacological Approaches (MAAP), Inserm ERL 1289, Université de Toulouse, CNRS, 31077 Toulouse, France.
  • Benoit-Vical F; Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III-Paul Sabatier (UPS), 31077 Toulouse, France.
  • Audran G; Aix-Marseille University, CNRS, Centrale Marseille ISM2, Case 531, Avenue Escadrille Normandie-Niemen, CEDEX 20, 13397 Marseille, France.
  • Mellet P; Université des Sciences et Techniques de Masuku, LASNSOM, Franceville BP 901, Gabon.
  • Boissier J; Laboratoire de Chimie de Coordination (LCC-CNRS) and, New Antimalarial Molecules and Pharmacological Approaches (MAAP), Inserm ERL 1289, Université de Toulouse, CNRS, 31077 Toulouse, France.
  • Marque SRA; Laboratoire de Chimie de Coordination (LCC-CNRS) and, New Antimalarial Molecules and Pharmacological Approaches (MAAP), Inserm ERL 1289, Université de Toulouse, CNRS, 31077 Toulouse, France.
Pathogens ; 13(6)2024 Jun 06.
Article en En | MEDLINE | ID: mdl-38921780
ABSTRACT
The expansion of drug resistant parasites sheds a serious concern on several neglected parasitic diseases. Our recent results on cancer led us to envision the use of peptide-alkoxyamines as a highly selective and efficient new drug against schistosome adult worms, the etiological agents of schistosomiasis. Indeed, the peptide tag of the hybrid compounds can be hydrolyzed by worm's digestive enzymes to afford a highly labile alkoxyamine which homolyzes spontaneously and instantaneously into radicals-which are then used as a drug against Schistosome adult parasites. This approach is nicely summarized as digging their graves with their forks. Several hybrid peptide-alkoxyamines were prepared and clearly showed an activity two of the tested compounds kill 50% of the parasites in two hours at a concentration of 100 µg/mL. Importantly, the peptide and alkoxyamine fragments that are unable to generate alkyl radicals display no activity. This strong evidence validates the proposed mechanism a specific activation of the prodrugs by the parasite proteases leading to parasite death through in situ alkyl radical generation.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Pathogens Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Pathogens Año: 2024 Tipo del documento: Article País de afiliación: Francia