Login / Signup

Stapled Phd Peptides Inhibit Doc Toxin Induced Growth Arrest in Salmonella .

Dennis J WormGrzegorz J GrabeGuilherme V de CastroSofya RabinovichIan WarmKira IsherwoodSophie HelaineAnna Barnard
Published in: ACS chemical biology (2023)
Bacterial toxin inhibition is a promising approach to overcoming antibiotic failure. In Salmonella , knockout of the toxin Doc has been shown to significantly reduce the formation of antibiotic-tolerant persisters. Doc is a kinase that is inhibited in nontolerant cells by its cognate antitoxin, Phd. In this work, we have developed first-in-class stapled peptide antitoxin mimetics based on the Doc inhibitory sequence of Phd. After making a series of substitutions to improve bacterial uptake, we identified a lead stapled Phd peptide that is able to counteract Doc toxicity in Salmonella . This provides an exciting starting point for the further development of therapeutic peptides capable of reducing antibiotic persistence in pathogenic bacteria.
Keyphrases
  • escherichia coli
  • listeria monocytogenes
  • induced apoptosis
  • oxidative stress
  • cell cycle arrest
  • drug induced
  • diabetic rats
  • cell cycle
  • cell death
  • heat shock
  • tyrosine kinase
  • heat shock protein