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
相关论文
共 50 条
  • [41] Discovery of inhibitors targeting protein tyrosine phosphatase 1B using a combined virtual screening approach
    Zhao, Dan
    Sun, Lu
    Zhong, Shijun
    MOLECULAR DIVERSITY, 2022, 26 (04) : 2159 - 2174
  • [42] Discovery of inhibitors targeting protein tyrosine phosphatase 1B using a combined virtual screening approach
    Dan Zhao
    Lu Sun
    Shijun Zhong
    Molecular Diversity, 2022, 26 : 2159 - 2174
  • [43] Protein-protein interaction-based high throughput screening for adenylyl cyclase 1 inhibitors: Design, implementation, and discovery of a novel chemotype
    Dwyer, Tiffany S. S.
    O'Brien, Joseph B. B.
    Ptak, Christopher P. P.
    LaVigne, Justin E. E.
    Flaherty, Daniel P. P.
    Watts, Val J. J.
    Roman, David L. L.
    FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [44] Virtual Screening and Experimental Validation Identify Novel Inhibitors of the Plasmodium falciparum Atg8-Atg3 Protein-Protein Interaction
    Hain, Adelaide U. P.
    Miller, Alexia S.
    Levitskaya, Jelena
    Bosch, Juergen
    CHEMMEDCHEM, 2016, 11 (08) : 900 - 910
  • [45] Discovery of small molecule inhibitors targeting the SUMO-SIM interaction using a protein interface consensus approach
    Voet, Arnout R. D.
    Ito, Akihiro
    Hirohama, Mikako
    Matsuoka, Seiji
    Tochio, Naoya
    Kigawa, Takanori
    Yoshida, Minoru
    Zhang, Kam Y. J.
    MEDCHEMCOMM, 2014, 5 (06) : 783 - 786
  • [46] Structure-based virtual screening toward the discovery of novel inhibitors for impeding the protein-protein interaction between HIV-1 integrase and human lens epithelium-derived growth factor (LEDGF/p75)
    Panwar, Umesh
    Singh, Sanjeev Kumar
    JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2018, 36 (12): : 3199 - 3217
  • [47] Discovery of novel inhibitors targeting enoyl-acyl carrier protein reductase in Plasmodium falciparum by structure-based virtual screening
    Nicola, George
    Smith, Colin A.
    Lucumi, Edinson
    Kuo, Mack R.
    Karagyozov, Luchezar
    Fidock, David A.
    Sacchettin, James C.
    Abagyan, Ruben
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 358 (03) : 686 - 691
  • [48] Discovery of small molecular inhibitors for interleukin-33/ST2 protein-protein interaction: a virtual screening, molecular dynamics simulations and binding free energy calculations
    Tan Thanh Mai
    Phuc Gia Nguyen
    Minh-Tri Le
    Thanh-Dao Tran
    Phuong Nguyen Hoai Huynh
    Dieu-Thuong Thi Trinh
    Quoc-Thai Nguyen
    Khac-Minh Thai
    MOLECULAR DIVERSITY, 2022, 26 (05) : 2659 - 2678
  • [49] Fluorophenols bearing nitrogenated heterocycle moieties, a class of novel Keap1-Nrf2 protein-protein interaction inhibitors: synthesis, antioxidant stress screening and molecular docking
    Feng, Xiu E.
    Kong, De Peng
    Ban, Shu Rong
    Ge, Rui
    Li, Qing Shan
    MEDICINAL CHEMISTRY RESEARCH, 2019, 28 (08) : 1319 - 1337
  • [50] Fluorophenols bearing nitrogenated heterocycle moieties, a class of novel Keap1-Nrf2 protein-protein interaction inhibitors: synthesis, antioxidant stress screening and molecular docking
    Xiu E Feng
    De Peng Kong
    Shu Rong Ban
    Rui Ge
    Qing Shan Li
    Medicinal Chemistry Research, 2019, 28 : 1319 - 1337