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  2. Zebrafish Yolk High Phosphoprotein-derived Peptide Pt5-1c Inhibits Methicillin-resistant Staphylococcus Aureus By Targeting The Cell Membrane With Associated Ribosomal Perturbation.
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  2. Zebrafish Yolk High Phosphoprotein-derived Peptide Pt5-1c Inhibits Methicillin-resistant Staphylococcus Aureus By Targeting The Cell Membrane With Associated Ribosomal Perturbation.

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Zebrafish yolk high phosphoprotein-derived peptide Pt5-1c inhibits methicillin-resistant Staphylococcus aureus by

Yazhuo Zhang1, Jia Liu1, Gehui Ren1

  • 1Lin He's Academician Workstation of New Medicine and Clinical Translation in Jining Medical University, Jining Medical University, Jining, 272067, China.

Fish & Shellfish Immunology
|November 23, 2025

View abstract on PubMed

Summary
This summary is machine-generated.
Keywords:
Cell membraneMethicillin-resistant Staphylococcus aureusPhosvitin

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Pt5-1c, an antibacterial peptide, effectively inhibits methicillin-resistant Staphylococcus aureus (MRSA) growth by disrupting its cell membrane. This peptide shows potential as a novel therapeutic agent against resistant bacterial infections.

Area of Science:

  • Biochemistry
  • Microbiology
  • Molecular Biology

Background:

  • Pt5-1c is an alpha-helical antibacterial peptide derived from zebrafish yolk high phosphoprotein.
  • Previous studies explored Pt5-1c's effects on common bacteria, but its impact on methicillin-resistant Staphylococcus aureus (MRSA) was unknown.

Purpose of the Study:

  • To investigate the specific effects of Pt5-1c on the growth and mechanisms of MRSA.

Main Methods:

  • MRSA was used as a model organism.
  • RNA-sequencing (RNA-seq) with Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis was performed.
  • Molecular docking was utilized to assess peptide-ribosome interactions.
  • Cell membrane permeability, depolarization, and intracellular content leakage were measured.

Main Results:

  • Pt5-1c significantly inhibited MRSA proliferation.
  • RNA-seq revealed upregulation of ribosome-related genes, but molecular docking showed weak, non-specific binding to the 70S ribosome.
  • Pt5-1c induced cell membrane permeability changes, depolarization, and leakage of intracellular contents, leading to cell lysis.

Conclusions:

  • Pt5-1c exhibits potent antibacterial activity against MRSA.
  • The primary mechanism involves direct damage to the bacterial cell membrane, leading to lysis, rather than ribosome inhibition.
  • Pt5-1c represents a promising candidate for developing new treatments against MRSA infections.