4.6 Article

Identification and optimization of an antimicrobial peptide from the ant venom toxin pilosulin

Journal

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 434, Issue 2, Pages 358-364

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2004.11.006

Keywords

antimicrobial peptide; sequence template; cytotoxicity; venom; pilosulin

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A template based on positional residue frequencies in the N-terminal stretch of natural a-helical antimicrobial peptides was used to prepare sequence patterns and to scan the Swiss-Prot Database, using the ScanProsite tool. This search identified a segment in pilosulin 1, a cytotoxic peptide from the venom of the jumper ant Myrmecia pilosula, as a potential novel antimicrobial peptide sequence. This segment, corresponding to the 20 N-terminal residues, was synthesized and its structural properties and biological activities were investigated. It showed a potent and broad spectrum antimicrobial activity including standard and multi-drug resistant gram-positive and gram-negative bacteria and Candida albicans, confirming the validity of the search method. A rational redesign approach resulting in four amino acid substitutions yielded a variant with improved antibacterial and significantly reduced hemolytic activity. (C) 2004 Elsevier Inc. All rights reserved.

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