Journal of the American Chemical Society · 2025 · 15 citations · 33 references
PharmacyMedicinal ChemistryMicrobiologyDrug DesignDrug DiscoveryLipid BiochemistryAntimicrobial PeptidesBiological MembranesLipid Bilayer StructureLipid BilayersLipid ChemistryMembrane EngineeringBacterial Membrane Lipid CompositionBroad-spectrum AntimicrobialsChemical Scaffold OptimizationLipopeptide TherapyMembrane Disruption MechanismsOuter Membrane StructureStructure - Activity Relationship OptimizationSynthetic Antimicrobial Peptide Design
Polymicrobial infections present considerable therapeutic challenges due to the absence of effective antimicrobial agents, particularly those involving both Gram-positive and Gram-negative bacteria. We hypothesize that antimicrobials rationally designed to target both the outer and inner membranes─distinct structural differences between these bacteria─could offer solutions to the therapeutic dilemmas of polymicrobial infections. Through lipid screening, we identified a promising lipid scaffold capable of disrupting the membrane system of both Gram-positive and Gram-negative bacteria. We developed a chemical optimization strategy to design an inverted-conical lipopeptide of LP 3K, which exhibits broad-spectrum antimicrobial activity against polymicrobial infections without the emergence of resistance. We further elucidated the structure–activity relationship and antimicrobial mechanisms of LP 3K . In a mouse model of polymicrobial infection, LP 3K demonstrated substantial antimicrobial and therapeutic effects, with confirmed in vivo biosafety. Our findings highlight the potential of lipopeptides as clinically translatable antimicrobials for the effective treatment of polymicrobial infections.
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Antimicrobial peptides of multicellular organisms
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