Phage Selection of Peptide Macrocycles against β-Catenin To Interfere with Wnt Signaling.

Détails

Ressource 1Télécharger: 70 Bertoldo 2016 ChemMedChem.pdf (2394.54 [Ko])
Etat: Public
Version: Final published version
Licence: Non spécifiée
ID Serval
serval:BIB_A9DB2F23A326
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Phage Selection of Peptide Macrocycles against β-Catenin To Interfere with Wnt Signaling.
Périodique
Chemmedchem
Auteur⸱e⸱s
Bertoldo D., Khan M.M., Dessen P., Held W., Huelsken J., Heinis C.
ISSN
1860-7187 (Electronic)
ISSN-L
1860-7179
Statut éditorial
Publié
Date de publication
2016
Peer-reviewed
Oui
Volume
11
Numéro
8
Pages
834-839
Langue
anglais
Résumé
Upregulation of β-catenin, the primary mediator of the Wnt signaling pathway, plays an important role in the tumorigenesis of several types of human cancer. Targeting β-catenin to interfere with its ability to serve as a translational co-activator is considered an attractive therapeutic approach. However, the development of inhibitors has been challenging because of the lack of obvious binding pockets for ligands, and because inhibitors should not interfere with other β-catenin functions. Only two ligands with known molecular interactions with β-catenin have been developed so far, and are based on stabilized α-helical peptides. In this study, we screened a large combinatorial library of bicyclic peptides by phage display. Binders to different surface regions of β-catenin were identified. The binding site of one group of ligands was mapped to the interaction region of the translational Wnt inhibitor ICAT (inhibitor of β-catenin and Tcf), which is a prime target site on β-catenin for therapeutic intervention, and to which no ligands could be developed before.
Pubmed
Web of science
Création de la notice
24/05/2016 17:25
Dernière modification de la notice
07/04/2021 6:34
Données d'usage