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2-氨基苯并咪唑衍生物作为选择性NOD1抑制剂的发现与表征

Discovery and characterization of 2-aminobenzimidazole derivatives as selective NOD1 inhibitors.

作者信息

Correa Ricardo G, Khan Pasha M, Askari Nadav, Zhai Dayong, Gerlic Motti, Brown Brock, Magnuson Gavin, Spreafico Roberto, Albani Salvatore, Sergienko Eduard, Diaz Paul W, Roth Gregory P, Reed John C

机构信息

Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.

出版信息

Chem Biol. 2011 Jul 29;18(7):825-32. doi: 10.1016/j.chembiol.2011.06.009.

Abstract

NLR family proteins play important roles in innate immune response. NOD1 (NLRC1) activates various signaling pathways including NF-κB in response to bacterial ligands. Hereditary polymorphisms in the NOD1 gene are associated with asthma, inflammatory bowel disease, and other disorders. Using a high throughput screening (HTS) assay measuring NOD1-induced NF-κB reporter gene activity, followed by multiple downstream counter screens that eliminated compounds impacting other NF-κB effectors, 2-aminobenzimidazole compounds were identified that selectively inhibit NOD1. Mechanistic studies of a prototypical compound, Nodinitib-1 (ML130; CID-1088438), suggest that these small molecules cause conformational changes of NOD1 in vitro and alter NOD1 subcellular targeting in cells. Altogether, this inaugural class of inhibitors provides chemical probes for interrogating mechanisms regulating NOD1 activity and tools for exploring the roles of NOD1 in various infectious and inflammatory diseases.

摘要

NLR家族蛋白在天然免疫反应中发挥重要作用。NOD1(NLRC1)响应细菌配体激活包括NF-κB在内的多种信号通路。NOD1基因的遗传性多态性与哮喘、炎症性肠病及其他疾病相关。通过一种高通量筛选(HTS)检测方法来测量NOD1诱导的NF-κB报告基因活性,随后进行多个下游反向筛选以排除影响其他NF-κB效应器的化合物,从而鉴定出了选择性抑制NOD1的2-氨基苯并咪唑化合物。对一种典型化合物Nodinitib-1(ML130;CID-1088438)的机制研究表明,这些小分子在体外引起NOD1的构象变化,并改变NOD1在细胞中的亚细胞定位。总之,这一开创性的抑制剂类别为探究调节NOD1活性的机制提供了化学探针,并为探索NOD1在各种感染性和炎症性疾病中的作用提供了工具。

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