Bristol-Myers Squibb, Princeton, NJ, USA.
Halda Therapeutics, Branford, CT, USA.
SLAS Discov. 2021 Feb;26(2):242-247. doi: 10.1177/2472555220919097. Epub 2020 May 13.
Hits from high-throughput screening (HTS) assays are typically evaluated using cheminformatics and/or empirical approaches before a decision for follow-up (activity confirmation and/or sample resynthesis) is made. However, the compound integrity (i.e., identity and purity) of these hits often remains largely unknown at this stage, since many compounds in the screening collection could undergo various changes such as degradation, polymerization, and precipitation during storage over time. When compound integrity is actually assessed for HTS hits postassay to address this issue, the process often increases the overall cycle time by weeks due to the reacquisition of the samples and the lengthy liquid chromatography-ultraviolet/mass spectrometric analysis time. Here we present a novel approach where compound integrity data are collected concurrently with the concentration-response curve (CRC) stage of HTS, with both assays occurring either in parallel on two distributions from the same liquid sample or serially using the original source liquid sample. The rapid generation of compound integrity data has been enabled by a high-speed ultra-high-pressure liquid chromatography-ultraviolet/mass spectrometric platform capable of analyzing ~2000 samples per instrument per week. From this parallel approach, both compound integrity and CRC potency results for screening hits become available to medicinal chemists at the same time, which has greatly enhanced the decision-making process for hit follow-up and progression. In addition, the compound integrity results from recent hits provide a real-time and representative "snapshot" of the sample integrity of the entire compound collection, and the data can be used for in-depth analyses of the screening collection.
高通量筛选 (HTS) 测定的命中结果通常在做出后续(活性确认和/或样品再合成)决定之前,使用化学信息学和/或经验方法进行评估。然而,在这个阶段,这些命中化合物的完整性(即身份和纯度)通常仍然很大程度上未知,因为筛选库中的许多化合物在储存过程中可能会发生各种变化,如降解、聚合和沉淀。当在测定后实际评估 HTS 命中化合物的完整性以解决此问题时,由于需要重新获取样品以及液相色谱-紫外/质谱分析时间较长,该过程通常会将总周期时间延长数周。在这里,我们提出了一种新方法,其中在 HTS 的浓度-反应曲线 (CRC) 阶段同时收集化合物完整性数据,这两种测定可以在同一液体样品的两个分布上平行进行,或者使用原始源液体样品串行进行。通过能够每周分析约 2000 个样品的高速超高效液相色谱-紫外/质谱平台,实现了化合物完整性数据的快速生成。通过这种平行方法,筛选命中的化合物完整性和 CRC 效力结果同时提供给药物化学家,这大大增强了对命中后续和进展的决策过程。此外,最近命中的化合物完整性结果实时提供了整个化合物库样品完整性的代表性“快照”,并且可以对筛选库进行深入分析。