虚拟筛选
药物发现
受体
对接(动物)
计算生物学
配体(生物化学)
跨膜蛋白
G蛋白偶联受体
药理学
生物信息学
化学
生物
医学
生物化学
护理部
作者
Daniel A. Greenfield,Hayden R. Schmidt,Meredith A. Skiba,Michael D. Mandler,Jacob R. Anderson,Piotr Sliz,Andrew C. Kruse
标识
DOI:10.1021/acsmedchemlett.9b00314
摘要
The σ1 receptor is a transmembrane protein implicated in several pathophysiological conditions, including neurodegenerative disease ( J. Pharmacol. Sci.201512711729), drug addiction ( Behav. Pharmacol.2016272–3 Spec Issue10015), cancer ( Handb. Exp. Pharmacol.2017244237308), and pain ( Neural Regener. Res.2018135775778). However, there are no high-throughput functional assays for σ1 receptor drug discovery. Here, we assessed high-throughput structure-based computational docking for discovery of novel ligands of the σ1 receptor. We screened a library of over 6 million compounds using the Schrödinger Glide package, followed by experimental characterization of top-scoring candidates. 77% of tested candidates bound σ1 with high affinity (KD < 1 μM). These include compounds with high selectivity for the σ1 receptor compared to the genetically unrelated but pharmacologically similar σ2 receptor, as well as compounds with substantial crossreactivity between the two receptors. These results establish structure-based virtual screening as a highly effective platform for σ1 receptor ligand discovery and provide compounds to prioritize in studies of σ1 biology.
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