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Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface

Intrinsically disordered protein YAP (yes-associated protein) interacts with TEADs transcriptional factors family (transcriptional enhancer associated domain) creating three interfaces. Interface 3, between the Ω-loop of YAP and a shallow pocket of TEAD was identified as the most important TEAD zone...

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Autores principales: Gibault, Floriane, Coevoet, Mathilde, Sturbaut, Manon, Farce, Amaury, Renault, Nicolas, Allemand, Frédéric, Guichou, Jean-François, Drucbert, Anne-Sophie, Foulon, Catherine, Magnez, Romain, Thuru, Xavier, Corvaisier, Matthieu, Huet, Guillemette, Chavatte, Philippe, Melnyk, Patricia, Bailly, Fabrice, Cotelle, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977113/
https://www.ncbi.nlm.nih.gov/pubmed/29738494
http://dx.doi.org/10.3390/cancers10050140
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author Gibault, Floriane
Coevoet, Mathilde
Sturbaut, Manon
Farce, Amaury
Renault, Nicolas
Allemand, Frédéric
Guichou, Jean-François
Drucbert, Anne-Sophie
Foulon, Catherine
Magnez, Romain
Thuru, Xavier
Corvaisier, Matthieu
Huet, Guillemette
Chavatte, Philippe
Melnyk, Patricia
Bailly, Fabrice
Cotelle, Philippe
author_facet Gibault, Floriane
Coevoet, Mathilde
Sturbaut, Manon
Farce, Amaury
Renault, Nicolas
Allemand, Frédéric
Guichou, Jean-François
Drucbert, Anne-Sophie
Foulon, Catherine
Magnez, Romain
Thuru, Xavier
Corvaisier, Matthieu
Huet, Guillemette
Chavatte, Philippe
Melnyk, Patricia
Bailly, Fabrice
Cotelle, Philippe
author_sort Gibault, Floriane
collection PubMed
description Intrinsically disordered protein YAP (yes-associated protein) interacts with TEADs transcriptional factors family (transcriptional enhancer associated domain) creating three interfaces. Interface 3, between the Ω-loop of YAP and a shallow pocket of TEAD was identified as the most important TEAD zone for YAP-TEAD interaction. Using the first X-ray structure of the hYAP(50–71)-hTEAD1(209–426) complex (PDB 3KYS) published in 2010, a protein-protein interaction inhibitors-enriched library (175,000 chemical compounds) was screened against this hydrophobic pocket of TEAD. Four different chemical families have been identified and evaluated using biophysical techniques (thermal shift assay, microscale thermophoresis) and in cellulo assays (luciferase activity in transfected HEK293 cells, RTqPCR in MDA-MB231 cells). A first promising hit with micromolar inhibition in the luciferase gene reporter assay was discovered. This hit also decreased mRNA levels of TEAD target genes.
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spelling pubmed-59771132018-05-31 Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface Gibault, Floriane Coevoet, Mathilde Sturbaut, Manon Farce, Amaury Renault, Nicolas Allemand, Frédéric Guichou, Jean-François Drucbert, Anne-Sophie Foulon, Catherine Magnez, Romain Thuru, Xavier Corvaisier, Matthieu Huet, Guillemette Chavatte, Philippe Melnyk, Patricia Bailly, Fabrice Cotelle, Philippe Cancers (Basel) Article Intrinsically disordered protein YAP (yes-associated protein) interacts with TEADs transcriptional factors family (transcriptional enhancer associated domain) creating three interfaces. Interface 3, between the Ω-loop of YAP and a shallow pocket of TEAD was identified as the most important TEAD zone for YAP-TEAD interaction. Using the first X-ray structure of the hYAP(50–71)-hTEAD1(209–426) complex (PDB 3KYS) published in 2010, a protein-protein interaction inhibitors-enriched library (175,000 chemical compounds) was screened against this hydrophobic pocket of TEAD. Four different chemical families have been identified and evaluated using biophysical techniques (thermal shift assay, microscale thermophoresis) and in cellulo assays (luciferase activity in transfected HEK293 cells, RTqPCR in MDA-MB231 cells). A first promising hit with micromolar inhibition in the luciferase gene reporter assay was discovered. This hit also decreased mRNA levels of TEAD target genes. MDPI 2018-05-08 /pmc/articles/PMC5977113/ /pubmed/29738494 http://dx.doi.org/10.3390/cancers10050140 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gibault, Floriane
Coevoet, Mathilde
Sturbaut, Manon
Farce, Amaury
Renault, Nicolas
Allemand, Frédéric
Guichou, Jean-François
Drucbert, Anne-Sophie
Foulon, Catherine
Magnez, Romain
Thuru, Xavier
Corvaisier, Matthieu
Huet, Guillemette
Chavatte, Philippe
Melnyk, Patricia
Bailly, Fabrice
Cotelle, Philippe
Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
title Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
title_full Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
title_fullStr Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
title_full_unstemmed Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
title_short Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
title_sort toward the discovery of a novel class of yap–tead interaction inhibitors by virtual screening approach targeting yap–tead protein–protein interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977113/
https://www.ncbi.nlm.nih.gov/pubmed/29738494
http://dx.doi.org/10.3390/cancers10050140
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