Structure and Dynamics of Cinnamycin-Lipid Complexes: Mechanisms of Selectivity for Phosphatidylethanolamine Lipids

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • Mikkel Vestergaard, Center for Insoluble Protein Structures (inSPIN)
  • ,
  • Nils Anton Berglund
  • Pin Chia Hsu, Center for Insoluble Protein Structures (inSPIN)
  • ,
  • Chen Song, Oxford University, Oxford, UK., Peking University
  • ,
  • Heidi Koldsø, Oxford University, Oxford, UK., Schrödinger LLC
  • ,
  • Birgit Schiøtt
  • Mark S.P. Sansom, Oxford University, Oxford, UK.

Cinnamycin is a lantibiotic peptide, which selectively binds to and permeabilizes membranes containing phosphatidylethanolamine (PE) lipids. As PE is a major component of many bacterial cell membranes, cinnamycin has considerable potential for destroying these. In this study, molecular dynamics simulations are used to elucidate the structure of a lipid-cinnamycin complex and the origin of selective lipid binding. The simulations reveal that cinnamycin selectively binds to PE by forming an extensive hydrogen-bonding network involving all three hydrogen atoms of the primary ammonium group of the PE head group. The substitution of a single hydrogen atom with a methyl group on the ammonium nitrogen destabilizes this hydrogen-bonding network. In addition to binding the primary ammonium group, cinnamycin also interacts with the phosphate group of the lipid through a previously uncharacterized phosphate-binding site formed by the backbone Phe10-Abu11-Phe12-Val13 moieties (Abu = 1-α-aminobutyric acid). In addition, hydroxylation of Asp15 at Cβ plays a role in selective binding of PE due to its tight interaction with the charged amine of the lipid head group. The simulations reveal that the position and orientation of the peptide in the membrane depend on the type of lipid to which it binds, suggesting a reason for why cinnamycin selectively permeabilizes PE-containing membranes.

Original languageEnglish
JournalACS Omega
Volume4
Issue20
Pages (from-to)18889-18899
Number of pages11
ISSN2470-1343
DOIs
Publication statusPublished - 2019

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