吡喃结构域
炎症体
化学
受体
重组DNA
计算生物学
药物发现
同源建模
G蛋白偶联受体
药物开发
模式识别受体
高通量筛选
效应器
生物化学
药理学
生物
药品
先天免疫系统
基因
酶
作者
Philip A. Harris,Chaya Duraiswami,Donald T. Fisher,James A. Fornwald,Sandra J. Hoffman,Glenn A. Hofmann,Ming Jiang,Ruth Lehr,Patricia McCormick,Leng Nickels,Benjamin J. Schwartz,Zining Wu,Guofeng Zhang,Robert W. Marquis,John Bertin,Peter J. Gough
标识
DOI:10.1016/j.bmcl.2015.05.032
摘要
Nod-like receptors (NLRs) are cytoplasmic pattern recognition receptors that are promising targets for the development of anti-inflammatory therapeutics. Drug discovery efforts targeting NLRs have been hampered by their inherent tendency to form aggregates making protein generation and the development of screening assays very challenging. Herein we report the results of an HTS screen of NLR family member NLRP1 (NLR family, pyrin domain-containing 1) which was achieved through the large scale generation of recombinant GST-His-Thrombin-NLRP1 protein. The screen led to the identification of a diverse set of ATP competitive inhibitors with micromolar potencies. Activity of these hits was confirmed in a FP binding assay, and two homology models were employed to predict the possible binding mode of the leading series and facilitate further lead-optimization. These results highlight a promising strategy for the identification of inhibitors of NLR family members which are rapidly emerging as key drivers of inflammation in human disease.
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