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首页> 外文期刊>Cancers >Toward the Discovery of a Novel Class of YAP–TEAD Interaction Inhibitors by Virtual Screening Approach Targeting YAP–TEAD Protein–Protein Interface
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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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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.
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hYAP 50-71 -hTEAD1 209-426复合物(PDB 3KYS)的第一个X射线结构,针对TEAD的这一疏水性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)鉴定和评估了四个不同的化学家族。发现了在荧光素酶基因报告基因分析中微摩尔抑制的第一个有希望的命中。这种打击还降低了TEAD靶基因的mRNA水平。

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