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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-5977113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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