Metal-ion Binding to Host Defense Peptide Piscidin 3 Observed in Phospholipid Bilayers by Magic Angle Spinning Solid-state NMR.
Ratan Kumar RaiAnna De AngelisAlexander GreenwoodStanley J OpellaMyriam L CottenPublished in: Chemphyschem : a European journal of chemical physics and physical chemistry (2018)
Cationic antimicrobial peptides (AMPs) are essential components of the innate immune system. They have attracted interest as novel compounds with the potential to treat infections associated with multi-drug resistant bacteria. In this study, we investigate piscidin 3 (P3), an AMP that was first discovered in the mast cells of hybrid striped bass. Prior studies showed that P3 is less active than its homolog piscidin 1 (P1) against planktonic bacteria. However, P3 has the advantage of being less toxic to mammalian cells and more active on biofilms and persister cells. Both P1 and P3 cross bacterial membranes and co-localize with intracellular DNA but P3 is more condensing to DNA while P1 is more membrane active. Recently, we showed that both peptides coordinate Cu2+ through an amino-terminal copper and nickel (ATCUN) motif. We also demonstrated that the bactericidal effects of P3 are linked to its ability to form radicals that nick DNA in the presence of Cu2+ . Since metal binding and membrane crossing by P3 is biologically important, we apply in this study solid-state NMR spectroscopy to uniformly 13 C-15 N-labeled peptide samples to structurally characterize the ATCUN motif of P3 bound to bilayers and coordinated to Ni2+ and Cu2+ . These experiments are supplemented with density functional theory calculations. Taken together, these studies refine the arrangement of not only the backbone but also side chain atoms of an AMP simultaneously bound to metal ions and phospholipid bilayers.
Keyphrases
- solid state
- drug resistant
- density functional theory
- molecular dynamics simulations
- circulating tumor
- cell free
- molecular dynamics
- single molecule
- metal organic framework
- immune response
- induced apoptosis
- multidrug resistant
- high resolution
- magnetic resonance
- protein kinase
- acinetobacter baumannii
- nucleic acid
- risk assessment
- aqueous solution
- quantum dots
- cell cycle arrest
- mass spectrometry
- transcription factor
- cell proliferation
- case control
- signaling pathway
- reduced graphene oxide
- human health