| Literature DB >> 30969469 |
Weining Zhao1, Ashley R Cross2,3,4, Caillan Crowe-McAuliffe5, Angela Weigert-Munoz1, Erika E Csatary6, Amy E Solinski6, Joanna Krysiak1, Joanna B Goldberg2,4,7, Daniel N Wilson5, Eva Medina8, William M Wuest4,6,7, Stephan A Sieber1.
Abstract
Natural products represent a rich source of antibiotics that address versatile cellular targets. The deconvolution of their targets via chemical proteomics is often challenged by the introduction of large photocrosslinkers. Here we applied elegaphenone, a largely uncharacterized natural product antibiotic bearing a native benzophenone core scaffold, for affinity-based protein profiling (AfBPP) in Gram-positive and Gram-negative bacteria. This study utilizes the alkynylated natural product scaffold as a probe to uncover intriguing biological interactions with the transcriptional regulator AlgP. Furthermore, proteome profiling of a Pseudomonas aeruginosa AlgP transposon mutant provided unique insights into the mode of action. Elegaphenone enhanced the elimination of intracellular P. aeruginosa in macrophages exposed to sub-inhibitory concentrations of the fluoroquinolone antibiotic norfloxacin.Entities:
Keywords: Pseudomonas aeruginosa; antibiotics; chemical proteomics; natural products; virulence
Year: 2019 PMID: 30969469 PMCID: PMC6555641 DOI: 10.1002/anie.201903472
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336