Journal article
L-type pyocins inhibit the BAM complex to kill without cell entry.
Fabian Munder, Matthew D Johnson, Imogen Samuels, Laura McCaughey, Oleksii Zdorevskyi, Chunxiao Wang, Ashleigh Kropp, Lauren Zavan, Erin P Price, Derek S Sarovich, Swati Varshney, Christopher A McDevitt, Hari Venugopal, Vivek Sharma, Matthew T Doyle, Francesca Short, Debnath Ghosal, James PR Connolly, Gavin J Knott, Rhys Grinter
Nat Commun | Published : 2026
Open access
Abstract
Many antibiotics are ineffective against the Gram-negative pathogen Pseudomonas aeruginosa because of intrinsic defence mechanisms, such as the impermeable bacterial outer membrane. Here, we show that protein antibiotics called L-type pyocins kill P. aeruginosa by inhibiting the β-barrel assembly machinery (BAM) complex at the cell surface, halting outer-membrane protein assembly. Using single-particle cryo-electron microscopy, we show that L-type pyocins bind a surface-exposed region of BamA and deploy a C-terminal peptide that competitively inhibits the BAM complex, demonstrating that cell entry is not required for antibiotic activity. We combine genetics, multi-omics and cryo-electron tom..
View full abstractRelated Projects (2)
Grants
Awarded by Department of Education and Training | Australian Research Council (ARC)
Awarded by Department of Health | National Health and Medical Research Council (NHMRC)