变构调节
化学
脂氧合酶
花生四烯酸
酶
代谢物
药物发现
生物化学
激活剂(遗传学)
花生四烯酸5-脂氧合酶
炎症
药理学
受体
生物
免疫学
作者
Hu Meng,Christopher L. McClendon,Ziwei Dai,Kenan Li,Xiaoling Zhang,Shan He,Erchang Shang,Ying Liu,Luhua Lai
标识
DOI:10.1021/acs.jmedchem.5b01011
摘要
For disease network intervention, up-regulating enzyme activities is equally as important as down-regulating activities. However, the design of enzyme activators presents a challenging route for drug discovery. Previous studies have suggested that activating 15-lipoxygenase (15-LOX) is a promising strategy to intervene the arachidonic acid (AA) metabolite network and control inflammation. To prove this concept, we used a computational approach to discover a previously unknown allosteric site on 15-LOX. Both allosteric inhibitors and novel activators were discovered using this site. The influence of activating 15-LOX on the AA metabolite network was then investigated experimentally. The activator was found to increase levels of 15-LOX products and reduce production of pro-inflammatory mediators in human whole blood assays. These results demonstrate the promising therapeutic value of enzyme activators and aid in further development of activators of other proteins.
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