蛋白质微阵列
微阵列
计算生物学
DNA微阵列
小分子
药物发现
微阵列分析技术
蛋白质-蛋白质相互作用
高通量筛选
生物
化学
生物信息学
基因
遗传学
基因表达
作者
Zhenkun Na,Sijun Pan,Mahesh Uttamchandani,Shao Q. Yao
标识
DOI:10.1007/978-1-4939-6584-7_10
摘要
Microarray screening technology has transformed the life sciences arena over the last decade. The platform is widely used in the area of mapping interaction networks, to molecular fingerprinting and small molecular inhibitor discovery. The technique has significantly impacted both basic and applied research. The microarray platform can likewise enable high-throughput screening and discovery of protein–protein interaction (PPI) inhibitors. Herein we demonstrate the application of microarray-guided PPI inhibitor discovery, using human BRCA1 as an example. Mutations in BRCA1 have been implicated in ~50 % of hereditary breast cancers. By targeting the (BRCT)2 domain, we showed compound 15a and its prodrug 15b inhibited BRCA1 activities in tumor cells. Unlike previously reported peptide-based PPI inhibitors of BRCA1, the compounds identified could be directly administered to tumor cells, thus making them useful in targeting BRCA1/PARP-related pathways involved in DNA damage and repair response, for cancer therapy.
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