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

被引:37
|
作者
Gibault, Floriane [1 ]
Coevoet, Mathilde [1 ]
Sturbaut, Manon [1 ]
Farce, Amaury [2 ]
Renault, Nicolas [2 ]
Allemand, Frederic [3 ]
Guichou, Jean-Francois [3 ]
Drucbert, Anne-Sophie [4 ]
Foulon, Catherine [4 ]
Magnez, Romain [1 ]
Thuru, Xavier [1 ]
Corvaisier, Matthieu [1 ]
Huet, Guillemette [1 ]
Chavatte, Philippe [2 ]
Melnyk, Patricia [1 ]
Bailly, Fabrice [1 ]
Cotelle, Philippe [1 ,5 ]
机构
[1] Univ Lille, CHU Lille, INSERM,UMR S 1172, JPArc,Ctr Rech Jean Pierre Aubert Neurosci & Canc, F-59000 Lille, France
[2] Univ Lille, CHU Lille, LIRIC Lille Inflammat Res Int Ctr, INSERM,U995, F-59000 Lille, France
[3] Univ Montpellier, Ctr Biochim Struct, CNRS, INSERM,U1054,UMR5048, 29 Rue Navacelles, F-34090 Montpellier, France
[4] Univ Lille, CHU Lille, Plate Forme Interact Mol, F-59000 Lille, France
[5] ENSCL, F-59000 Lille, France
关键词
protein-protein interaction; YAP-TEAD disruption; molecular docking; binding assays; anticancer; ORGAN SIZE CONTROL; HIPPO PATHWAY; DOWNSTREAM EFFECTORS; CELL-PROLIFERATION; EMERGING ROLES; CANCER; YAP/TAZ; TAZ; COACTIVATORS; COMPLEX;
D O I
10.3390/cancers10050140
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Intrinsically disordered protein YAP (yes-associated protein) interacts with TEADs transcriptional factors family (transcriptional enhancer associated domain) creating three interfaces. Interface 3, between the Omega-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.
引用
收藏
页数:14
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