| Literature DB >> 28089350 |
Travis R Helgren1, Congling Chen1, Phumvadee Wangtrakuldee1, Thomas E Edwards2, Bart L Staker3, Jan Abendroth2, Banumathi Sankaran4, Nicole A Housley5, Peter J Myler6, Jonathon P Audia5, James R Horn1, Timothy J Hagen7.
Abstract
Methionine aminopeptidase (MetAP) is a class of ubiquitous enzymes essential for the survival of numerous bacterial species. These enzymes are responsible for the cleavage of N-terminal formyl-methionine initiators from nascent proteins to initiate post-translational modifications that are often essential to proper protein function. Thus, inhibition of MetAP activity has been implicated as a novel antibacterial target. We tested this idea in the present study by targeting the MetAP enzyme in the obligate intracellular pathogen Rickettsia prowazekii. We first identified potent RpMetAP inhibitory species by employing an in vitro enzymatic activity assay. The molecular docking program AutoDock was then utilized to compare published crystal structures of inhibited MetAP species to docked poses of RpMetAP. Based on these in silico and in vitro screens, a subset of 17 compounds was tested for inhibition of R. prowazekii growth in a pulmonary vascular endothelial cell (EC) culture infection model system. All compounds were tested over concentration ranges that were determined to be non-toxic to the ECs and 8 of the 17 compounds displayed substantial inhibition of R. prowazekii growth. These data highlight the therapeutic potential for inhibiting RpMetAP as a novel antimicrobial strategy and set the stage for future studies in pre-clinical animal models of infection.Entities:
Keywords: Epidemic typhus; Inhibition; Lung endothelial cells; MetAP; Metalloenzyme; Methionine aminopeptidase; Rickettsia prowazekii
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Year: 2016 PMID: 28089350 PMCID: PMC5319851 DOI: 10.1016/j.bmc.2016.11.013
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641