AI Article Synopsis

  • Natural products, like elegaphenone, are valuable sources of antibiotics that can target various cellular functions, but pinpointing their specific targets is often complicated by bulky chemical tags.
  • Researchers used elegaphenone, which has a natural structure with a benzophenone core, to study its interactions in both Gram-positive and Gram-negative bacteria.
  • The study revealed that elegaphenone interacts with the transcription regulator AlgP and boosts the effectiveness of norfloxacin in reducing Pseudomonas aeruginosa levels within macrophages.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555641PMC
http://dx.doi.org/10.1002/anie.201903472DOI Listing

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