化学
化学图书馆
排名(信息检索)
虚拟筛选
组合化学
产量(工程)
计算生物学
药物发现
小分子
概率逻辑
化学合成
结合位点
色谱法
斯卡查德图
化学数据库
高通量筛选
配体结合分析
数据挖掘
立体化学
分析物
肽库
分子
结构-活动关系
生物化学
血浆蛋白结合
滴定法
相对标准差
结合亲和力
分子模型
作者
John C. Faver,Flora Sundersingh,Lauren A. Viarengo-Baker,Ying-Chu Chen,Katelyn Billings,Patrick Riley,Ching-Hsuan Tsai,Christopher S. Kollmann
标识
DOI:10.1021/acs.jmedchem.5c02259
摘要
DNA-encoded chemical libraries (DELs) enable the highly efficient screening of billions of small molecules for binding to a target of interest and provide valuable training data for machine learning models for virtual screening. However, DEL screening data are notoriously noisy due in large part to significant variance in the synthetic yield of library members. Here, we show an analysis from a split-sample DEL screening strategy against Bruton's tyrosine kinase (BTK), which includes a panel of affinity selections against the target at varying concentrations and a probabilistic model to estimate the binding affinity and relative input concentrations of library members. We compared model predictions to SPR measurements of resynthesized DNA-conjugated compounds and found that this methodology yielded an improved ranking of library members by binding affinity compared to enrichment metrics. Additionally, the method successfully recovered a library member with a potent binding affinity that would not have been detected in our standard DEL selection.
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