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Influence of pH on the activity of thrombin-derived antimicrobial peptides

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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  1. Concentration- and pH-Dependent Oligomerization of the Thrombin-Derived C-Terminal Peptide TCP-25

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Thrombin-derived C-terminal fragments aggregate and scavenge bacteria and their proinflammatory products

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. A C-terminal peptide of TFPI-1 facilitates cytosolic delivery of nucleic acid cargo into mammalian cells

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  4. A dual-action peptide-containing hydrogel targets wound infection and inflammation

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  5. Degradable dendritic nanogels as carriers for antimicrobial peptides

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  • Daniel A Holdbrook
  • Shalini Singh
  • Yeu Khai Choong
  • Jitka Petrlova
  • Martin Malmsten
  • Peter J Bond
  • Navin Kumar Verma
  • Artur Schmidtchen
  • Rathi Saravanan
Vis graf over relationer

The wound environment is characterized by physiological pH changes. Proteolysis of thrombin by wound-derived proteases, such as neutrophil elastase, generates antimicrobial thrombin-derived C-terminal peptides (TCPs), such as HVF18 (HVFRLKKWIQKVIDQFGE). Presence of such TCPs in human wound fluids in vivo, as well as the occurrence of an evolutionarily conserved His residue in the primary amino acid sequence of TCPs, prompted us to investigate the pH-dependent antibacterial action of HVF18, as well as of the prototypic GKY25 (GKYGFYTHVFRLKKWIQKVIDQFGE). We show that protonation of this His residue at pH 5.5 increases the antibacterial activity of both TCPs against Gram-negative Escherichia coli by membrane disruption. Physiological salt level (150 mM NaCl) augments antibacterial activity of GKY25 but diminishes for the shorter HVF18. Replacing His with Leu or Ser in GKY25 abolishes the His protonation-dependent increase in antibacterial activity at pH 5.5, whereas substitution with Lys maintains activity at neutral (pH 7.4) and acidic pH. Interestingly, both TCPs display decreased binding affinities to human CD14 with decreasing pH, suggesting a likely switch in mode-of-action, from anti-inflammatory at neutral pH to antibacterial at acidic pH. Together, the results demonstrate that apart from structural prerequisites such as peptide length, charge, and hydrophobicity, the evolutionarily conserved His residue of TCPs influences their antibacterial effects and reveals a previously unknown aspect of TCPs biological action.

OriginalsprogEngelsk
TidsskriftBiochimica et Biophysica Acta - Biomembranes
Vol/bind1860
Udgave nummer11
Sider (fra-til)2374-2384
Antal sider11
ISSN0005-2736
DOI
StatusUdgivet - nov. 2018

ID: 56331815