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Antimicrobial Agents and Chemotherapy, October 2006, p. 3330-3335, Vol. 50, No. 10
0066-4804/06/$08.00+0 doi:10.1128/AAC.00455-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 790-784, Korea
Received 11 April 2006/ Returned for modification 26 May 2006/ Accepted 14 July 2006
Amphipathic antimicrobial peptides can destroy bacteria cells by inducing membrane permeabilization, forming one strategy for innate defense by various organisms. However, although the antimicrobial peptides are considered a promising alternative for use against multidrug-resistant bacteria, large-scale screening of potential candidate antimicrobial peptides will require a simple, rapid assay for antimicrobial activity. Here, we describe a novel fluorescence resonance energy transfer (FRET)-based assay system for antimicrobial peptides which takes advantage of pH-related changes in FRET efficiency due to the instability of enhanced yellow fluorescent protein versus the stability of enhanced cyan fluorescent protein in a reduced-pH environment. We successfully showed that quantification of antimicrobial activity is possible through a difference of FRET efficiency between ECFP-EYFP fusion molecules released from disrupted Escherichia coli in an extracellular environment (pH 6) and those retained in an intracellular environment (pH
7). Thus, we herein suggest a new simple, effective, and efficient pH-controlled FRET-based antimicrobial peptide screening method applicable to high-throughput screening of candidate peptide libraries.
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