Journal of Medicinal Chemistry · 2015 · 52 citations · 38 references
Life SciencesBiochemistryPharmacologyDrug DesignDrug DiscoveryInflammationAllosteric Drug DesignAllosteric RegulationEnzyme ActivatorsEnzyme AssaysEnzyme DiscoveryEnzyme InhibitionAllosteric ActivationAllosteric Drug DiscoveryAllosteric Enzyme ActivationAllosteric Regulation Of MetabolismAllosteric Site MappingAllosteric Site TargetingArachidonic Acid MetabolitesComputational Allosteric Design
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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