Shortened cecropin A‐melittin hybrids Significant size reduction retains potent antibiotic activity
- 16 January 1992
- journal article
- Published by Wiley in FEBS Letters
- Vol. 296 (2) , 190-194
- https://doi.org/10.1016/0014-5793(92)80377-s
Abstract
We have earlier reported two 26‐residue antibacterial peptides made up from different segments ol'cecropin A (CA) and melittin (M). We now report a substantial reduction in size at the C‐terminal section of the highly active hybrid CA(1–8)M(1–18), leading to a series of 20‐, 18‐ and 15‐residue analogs with antibiotic properties similar to the larger molecule. In particular, the 15‐residue hybrids CA(1–7)M(2–9), CA(1–7)M(4–11) and CA(1–7)M(5–12) are the shortest cecropin‐based peptide antibiotics described so far, with antibacterial activity and spectra similar or better than cecropin A and a 60% reduction in size. Their reduced size and highly α‐helical structure require an alternative mechanism for their interaction with bacterial membranes.Keywords
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