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2000
Volume 9, Issue 4
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

CRAMP-18 is an 18-residue functional region, corresponding to residues 16-33 of a mouse-derived antibiotic peptide CRAMP. To develop novel antibiotic peptides possessing strong antibiotic activity against bacterial, fungal and tumor cells without hemolytic activity, three analogs of CRAMP-18 were synthesized containing either Leu- or Lys-substitution. Leusubstitution ([L1, 8]-CRAMP-18) in the hydrophobic helix face of CRAMP-18 induced a dramatic increase in antibiotic activity without a significant increase in hemolytic activity. Lys-substitution ([K2, 13]-CRAMP-18 or [K9, 16]-CRAMP-18) in the hydrophilic helix face produced a smaller response. Therefore, [L1, 8]-CRAMP-18 may be an attractive candidate for developing novel peptide antibiotics.

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/content/journals/ppl/10.2174/0929866023408643
2002-08-01
2025-11-04
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/content/journals/ppl/10.2174/0929866023408643
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  • Article Type:
    Review Article
Keyword(s): Cramp Analog; Hemolytic; hydrophobic helix face; peptide CRAMP
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