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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:通过针对YAP-TEAD蛋白质-蛋白质界面的虚拟筛选方法发现一类新型的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:本质上无序的蛋白YAP(是相关蛋白)与TEADs转录因子家族(转录增强子相关域)相互作用,产生三个界面。 YAP的Ω回路和TEAD的浅凹区之间的界面3被确定为YAP-TEAD相互作用的最重要的TEAD区。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,针对TEAD的这个疏水口袋筛选了富含蛋白质-蛋白质相互作用抑制剂的文库(175,000个化学化合物)。已使用生物物理技术(热位移测定,微尺度热泳)和纤维素测定(转染的HEK293细胞中的萤光素酶活性,MDA-MB231细胞中的RTqPCR)鉴定并评估了四个不同的化学家族。在萤光素酶基因报告基因检测中发现了第一个有希望的具有微摩尔抑制作用的命中物。这种打击还降低了TEAD靶基因的mRNA水平。

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