4.6 Article

How Many Antimicrobial Peptide Molecules Kill a Bacterium? The Case of PMAP-23

Journal

ACS CHEMICAL BIOLOGY
Volume 9, Issue 9, Pages 2003-2007

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cb500426r

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Funding

  1. Italian Ministry of Education, University and Research [2010NRREPL_008]
  2. National Research Foundation of Korea [2011-0017532]
  3. National Research Foundation of Korea [2011-0017532] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Antimicrobial peptides (AMPs) kill bacteria mainly through the perturbation of their membranes and are promising compounds to fight drug resistance. Models of the mechanism of AMPs-induced membrane perturbation were developed based on experiments in liposomes, but their relevance for bacterial killing is debated. We determined the association of an analogue of the AMP PMAP-23 to Escherichia coli cells, under the same experimental conditions used to measure bactericidal activity. Killing took place only when bound peptides completely saturated bacterial membranes (10(6)-10(7) bound peptides per cell), indicating that the carpet model for the perturbation of artificial bilayers is representative of what happens in real bacteria. This finding supports the view that, at least for this peptide, a microbicidal mechanism is possible in vivo only at micromolar total peptide concentrations. We also showed that, notwithstanding their simplicity, liposomes represent characterize AMPs partition in bacterial membranes.

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