Lee Jonathan A, Chu Shaoyou, Willard Francis S, Cox Karen L, Sells Galvin Rachelle J, Peery Robert B, Oliver Sarah E, Oler Jennifer, Meredith Tamika D, Heidler Steven A, Gough Wendy H, Husain Saba, Palkowitz Alan D, Moxham Christopher M
Department of Quantitative and Structural Biology, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA.
J Biomol Screen. 2011 Jul;16(6):588-602. doi: 10.1177/1087057111405379. Epub 2011 Apr 26.
Phenotypic lead generation strategies seek to identify compounds that modulate complex, physiologically relevant systems, an approach that is complementary to traditional, target-directed strategies. Unlike gene-specific assays, phenotypic assays interrogate multiple molecular targets and signaling pathways in a target "agnostic" fashion, which may reveal novel functions for well-studied proteins and discover new pathways of therapeutic value. Significantly, existing compound libraries may not have sufficient chemical diversity to fully leverage a phenotypic strategy. To address this issue, Eli Lilly and Company launched the Phenotypic Drug Discovery Initiative (PD(2)), a model of open innovation whereby external research groups can submit compounds for testing in a panel of Lilly phenotypic assays. This communication describes the statistical validation, operations, and initial screening results from the first PD(2) assay panel. Analysis of PD(2) submissions indicates that chemical diversity from open source collaborations complements internal sources. Screening results for the first 4691 compounds submitted to PD(2) have confirmed hit rates from 1.6% to 10%, with the majority of active compounds exhibiting acceptable potency and selectivity. Phenotypic lead generation strategies, in conjunction with novel chemical diversity obtained via open-source initiatives such as PD(2), may provide a means to identify compounds that modulate biology by novel mechanisms and expand the innovation potential of drug discovery.
表型先导物发现策略旨在识别能够调节复杂的、与生理相关系统的化合物,这是一种与传统的靶向策略互补的方法。与基因特异性检测不同,表型检测以一种“无靶点”的方式探究多个分子靶点和信号通路,这可能揭示已深入研究的蛋白质的新功能,并发现具有治疗价值的新通路。值得注意的是,现有的化合物库可能没有足够的化学多样性来充分利用表型策略。为了解决这个问题,礼来公司发起了表型药物发现计划(PD(2)),这是一种开放式创新模式,外部研究团队可以提交化合物,在礼来的一组表型检测中进行测试。本通讯描述了首个PD(2)检测小组的统计验证、操作及初步筛选结果。对PD(2)提交物的分析表明,开源合作带来的化学多样性补充了内部来源。提交给PD(2)的前4691种化合物的筛选结果证实,命中率在1.6%至10%之间,大多数活性化合物表现出可接受的效力和选择性。表型先导物发现策略,与通过诸如PD(2)这样的开源计划获得的新型化学多样性相结合,可能提供一种手段来识别通过新机制调节生物学过程的化合物,并扩大药物发现的创新潜力。