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Targeting the Pentose Phosphate Pathway: Characterization of a New 6PGL Inhibitor.
Tran, Anh Tuan; Sadet, Aude; Calligari, Paolo; Lopes, Philippe; Ouazzani, Jamal; Sollogoub, Matthieu; Miclet, Emeric; Abergel, Daniel.
  • Tran AT; Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, 75005 Paris, France.
  • Sadet A; Laboratoire des Biomolécules, LBM, Département de Chimie, École Normale Supérieure, PSL University, Sorbonne Université, CNRS, 75005 Paris, France.
  • Calligari P; Dipartimento di Scienze e Tecnologie Chimiche, Università di Roma Tor Vergata, Via della Ricerca Scientifica, Rome, Italy.
  • Lopes P; Institut de Chimie des Substances Naturelles, UPR 2301, CNRS, 91272 Gif sur Yvette, France.
  • Ouazzani J; Institut de Chimie des Substances Naturelles, UPR 2301, CNRS, 91272 Gif sur Yvette, France.
  • Sollogoub M; Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, 75005 Paris, France.
  • Miclet E; Sorbonne Université, École Normale Supérieure, PSL University, CNRS, Laboratoire des Biomolécules, LBM, 75005 Paris, France. Electronic address: emeric.miclet@sorbonne-universite.fr.
  • Abergel D; Laboratoire des Biomolécules, LBM, Département de Chimie, École Normale Supérieure, PSL University, Sorbonne Université, CNRS, 75005 Paris, France.
Biophys J ; 115(11): 2114-2126, 2018 12 04.
Article en En | MEDLINE | ID: mdl-30467026
Human African trypanosomiasis, or sleeping sickness, is a lethal disease caused by the protozoan parasite Trypanosoma brucei. However, although many efforts have been made to understand the biochemistry of this parasite, drug development has led to treatments that are of limited efficiency and of great toxicity. To develop new drugs, new targets must be identified, and among the several metabolic processes of trypanosomes that have been proposed as drug targets, carbohydrate metabolism (glycolysis and the pentose phosphate pathway (PPP)) appears as a promising one. As far as the PPP is concerned, a limited number of studies are related to the glucose-6-phosphate dehydrogenase. In this work, we have focused on the activity of the second PPP enzyme (6-phospho-gluconolactonase (6PGL)) that transforms 6-phosphogluconolactone into 6-phosphogluconic acid. A lactam analog of the natural substrate has been synthesized, and binding of the ligand to 6PGL has been investigated by NMR titration. The ability of this ligand to inhibit 6PGL has also been demonstrated using ultraviolet experiments, and protein-inhibitor interactions have been investigated through docking calculations and molecular dynamics simulations. In addition, a marginal inhibition of the third enzyme of the PPP (6-phosphogluconate dehydrogenase) was also demonstrated. Our results thus open new prospects for targeting T. brucei.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vía de Pentosa Fosfato / Fosfogluconato Deshidrogenasa / Trypanosoma brucei brucei / Hidrolasas de Éster Carboxílico / Inhibidores Enzimáticos / Lactamas Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vía de Pentosa Fosfato / Fosfogluconato Deshidrogenasa / Trypanosoma brucei brucei / Hidrolasas de Éster Carboxílico / Inhibidores Enzimáticos / Lactamas Idioma: En Año: 2018 Tipo del documento: Article