| Literature DB >> 26290290 |
Hu Meng, Christopher L McClendon1, Ziwei Dai, Kenan Li, Xiaoling Zhang, Shan He, Erchang Shang, Ying Liu, Luhua Lai.
Abstract
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.Entities:
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Year: 2015 PMID: 26290290 DOI: 10.1021/acs.jmedchem.5b01011
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446