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Antimicrobial Agents and Chemotherapy, December 2008, p. 4463-4465, Vol. 52, No. 12
0066-4804/08/$08.00+0 doi:10.1128/AAC.00810-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Microbiology and Molecular Genetics and Center for Biopreparedness and Infectious Disease,1 Department of Biophysics, Medical College of Wisconsin, Milwaukee, Wisconsin 532262
Received 19 June 2008/ Returned for modification 4 August 2008/ Accepted 7 October 2008
Lysine-enriched analogs of the cecropin-mellitin hybrid peptide, CA1-7 M2-9 (designated CM15), designed with optimized amphipathicity, retained antimicrobial activities similar to that of wild-type CM15 and had substantially reduced levels of hemolytic activity and cytotoxicity toward cultured macrophages, resulting in enhanced selectivity. These lysine-enriched analogs provide templates for improved CM15 peptide or peptidomimetic antibiotics.
Published ahead of print on 13 October 2008.
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