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Protein-inspired antibiotics active against vancomycin- and daptomycin-resistant bacteria.

Mark A T BlaskovichKarl A HansfordYujing GongMark S ButlerCraig MuldoonJohnny X HuangSoumya RamuAlberto B SilvaMu ChengAngela M KavanaghZyta Maria ZioraRajaratnam PremrajFredrik LindahlTanya A BradfordJune C LeeTomislav KaroliRuby PelingonDavid J EdwardsMaite AmadoAlysha G ElliottWanida PhetsangNoor Huda DaudJohan E DeeckeHanna E SidjabatSefetogi RamaologaJohannes ZueggJason R BetleyAndrew P G BeeversRichard A G SmithJason A RobertsDavid L PatersonMatthew A Cooper
Published in: Nature communications (2018)
The public health threat posed by a looming 'post-antibiotic' era necessitates new approaches to antibiotic discovery. Drug development has typically avoided exploitation of membrane-binding properties, in contrast to nature's control of biological pathways via modulation of membrane-associated proteins and membrane lipid composition. Here, we describe the rejuvenation of the glycopeptide antibiotic vancomycin via selective targeting of bacterial membranes. Peptide libraries based on positively charged electrostatic effector sequences are ligated to N-terminal lipophilic membrane-insertive elements and then conjugated to vancomycin. These modified lipoglycopeptides, the 'vancapticins', possess enhanced membrane affinity and activity against methicillin-resistant Staphylococcus aureus (MRSA) and other Gram-positive bacteria, and retain activity against glycopeptide-resistant strains. Optimised antibiotics show in vivo efficacy in multiple models of bacterial infection. This membrane-targeting strategy has potential to 'revitalise' antibiotics that have lost effectiveness against recalcitrant bacteria, or enhance the activity of other intravenous-administered drugs that target membrane-associated receptors.
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