Journal of the American Chemical Society · 2008 · 177 citations · 25 references
Life SciencesBiochemistryMicrobiologyAntimicrobial ResistanceDrug DesignDrug DiscoveryAntibiotic ResistanceAntibiotic Resistance MechanismsAntimicrobial ToxicityBiological MembranesLipid Bilayer StructureLipid ChemistryAntibacterial Drug DevelopmentAntibiotic DiscoveryAntimicrobial Drug DevelopmentBacterial Membrane Lipid CompositionDrug - Membrane InteractionsMembrane-active AntibioticsNovel Antibacterial Drug DiscoverySelectivity
A wide range of chemical structures having antimicrobial activity have been studied in an effort to treat the increasing emergence of bacteria that are resistant to traditional antibiotics. These agents have varying degrees of toxicity against different bacterial species. We demonstrate, using members of a novel class of antimicrobial agents, the oligomers of acyllysine, that one cause for the difference in species selectivity is the ability to induce the clustering of anionic lipids, resulting in their segregation into domains. This phenomenon occurs only in bacterial membranes composed of both anionic and zwitterionic lipids and not with bacteria whose membrane lipids are largely anionic. As a consequence it can be predicted which bacterial species will be most affected by antimicrobial agents that function principally by this mechanism. This finding allows for the design of new antibiotics with selective toxicity against different groups of bacteria.
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Antimicrobial peptides of multicellular organisms
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Use of the Cell Wall Precursor Lipid II by a Pore-Forming Peptide Antibiotic
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