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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

机译:通过虚拟筛选方法瞄准YAP-Tead蛋白蛋白界面的虚拟筛选方法发现新类别的YAP-Tead相互作用抑制剂

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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 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 hYAP50–71-hTEAD1209–426 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.
机译:本质无序的蛋白质yap(yes-相关蛋白)与Tead转录因子家族(转录增强子相关域)相互作用,从而创建三个接口。界面3,在YAP的ω环之间和Tead的浅袋之间被识别为YAP-Tead相互作用的最重要的Tead带。使用2010年发布的HYAP50-71-HTEAD1209-426复合物(PDB 3KYS)的第一个X射线结构,筛选富含蛋白质 - 蛋白质相互作用抑制剂的富含抑制剂(175,000种化合物),筛选抗ead的这种疏水口袋。已经使用生物物理技术(热移测测定,微观致密镜)和纤维运动测定(转染HEK293细胞中的荧光素酶活性,MDA-MB231细胞中的RTQPCR)进行了鉴定和评估了四种不同的化学系列。发现了在荧光素酶基因报告分析中具有微摩罗尔抑制的第一个有希望的击中。这种受到抗ea靶基因的mRNA水平。

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