连环素
选择性
化学
淋巴瘤
细胞
癌症研究
计算生物学
分子生物学
生物化学
生物
基因
Wnt信号通路
免疫学
催化作用
作者
Min Zhang,John A. Wisniewski,Haitao Ji
标识
DOI:10.1016/j.ab.2014.09.018
摘要
The aberrant formation of the β-catenin/B-cell lymphoma 9 (BCL9) protein-protein complex is the driving force for many diseases, including cancer. Crystallographic analyses demonstrate that the surface area in β-catenin for interacting with BCL9 is overlapped with that for the β-catenin/E-cadherin interaction. In this study, a robust AlphaScreen selectivity assay was developed to quantify inhibitor potency for the β-catenin/BCL9 interaction and selectivity for β-catenin/BCL9 over β-catenin/E-cadherin interactions. A pilot screen was performed to demonstrat the feasibility of this assay. This selectivity assay is highly sensitive and suitable for adaptation to high-throughput screening. The establishment of this assay lays the foundation for the discovery of selective inhibitors specific for β-catenin/BCL9 interactions.
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