Bisbenzimidazole derivatives as potent inhibitors of the trypsin-like sites of the immunoproteasome core particle - Université Pierre et Marie Curie Accéder directement au contenu
Article Dans Une Revue Biochimie Année : 2015

Bisbenzimidazole derivatives as potent inhibitors of the trypsin-like sites of the immunoproteasome core particle

Olga N. Koroleva
  • Fonction : Auteur
The Hien Pham
  • Fonction : Auteur
Dominique Bouvier
  • Fonction : Auteur
Laure Dufau
  • Fonction : Auteur
Lixian Qin
  • Fonction : Auteur
Alexander A. Ivanov
  • Fonction : Auteur
Alexei L. Zhuze
  • Fonction : Auteur
Elizaveta S. Gromova
  • Fonction : Auteur

Résumé

In this study, a monomeric (MB) and a dimeric (DB) bisbenzimidazoles were identified as novel proteasome inhibitors of the trypsin-like activity located on beta 2c sites of the constitutive 20S proteasome (IC50 values at 2-4 mu M range). Remarkably, they were further shown to be 100- and 200-fold more potent inhibitors of the immunoproteasome trypsin-like activity (beta 2i sites, IC50 = 24 nM) than of the homologous constitutive activity. Molecular models of inhibitor/enzyme complexes in the two types of trypsin-like sites and corresponding computed binding energy values corroborated kinetic data. Different binding modes were suggested for MB and DB to the beta 2c and beta 2i trypsic sites. Each pointed to better contacts of the ligand inside the beta 2i active site than for beta 2c site. MB and DB represent the first selective inhibitors of the immunoproteasome trypsin-like activity described to date and can be considered as prototypes for inhibiting this activity.
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Dates et versions

hal-01544056 , version 1 (21-06-2017)

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Citer

Olga N. Koroleva, The Hien Pham, Dominique Bouvier, Laure Dufau, Lixian Qin, et al.. Bisbenzimidazole derivatives as potent inhibitors of the trypsin-like sites of the immunoproteasome core particle. Biochimie, 2015, 108, pp.94-100. ⟨10.1016/j.biochi.2014.11.002⟩. ⟨hal-01544056⟩
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