Biochemical Technologies, Science and Technology Division, Corning Inc., Corning, NY 14831, USA.
Sci Rep. 2011;1:33. doi: 10.1038/srep00033. Epub 2011 Jul 7.
We describe a label-free integrative pharmacology on-target (iPOT) method to assess the pharmacology of drugs at the β(2)-adrenergic receptor. This method combines dynamic mass redistribution (DMR) assays using an array of probe molecule-hijacked cells with similarity analysis. The whole cell DMR assays track cell system-based, ligand-directed, and kinetics-dependent biased activities of the drugs, and translates their on-target pharmacology into numerical descriptors which are subject to similarity analysis. We demonstrate that the approach establishes an effective link between the label-free pharmacology and in vivo therapeutic indications of drugs.
我们描述了一种无标记的整合药理学靶标(iPOT)方法,用于评估β(2)-肾上腺素能受体的药物药理学。该方法将使用探针分子劫持细胞的阵列的动态质量重分布(DMR)测定与相似性分析相结合。全细胞 DMR 测定跟踪基于细胞系统、配体导向和动力学依赖性的药物偏向活性,并将其靶标药理学转化为可进行相似性分析的数值描述符。我们证明该方法在无标记药理学和药物的体内治疗指征之间建立了有效的联系。