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Interaction of Protegrin-1 with Lipid Bilayers: Membrane Thinning Effect
by
Nussinov, Ruth
, Woolf, Thomas B.
, Ma, Buyong
, Jang, Hyunbum
in
Amino acids
/ Antimicrobial Cationic Peptides - chemistry
/ Biophysical Theory and Modeling
/ Cells
/ Computer Simulation
/ Effects
/ Lipid Bilayers - chemistry
/ Lipids
/ Membranes
/ Microorganisms
/ Models, Molecular
/ Peptides
/ Peptides - chemistry
/ Phosphatidylcholines - chemistry
/ Phosphatidylglycerols - chemistry
/ Protein Structure, Secondary
/ Proteins - chemistry
/ Thinning
/ Water - chemistry
2006
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Interaction of Protegrin-1 with Lipid Bilayers: Membrane Thinning Effect
by
Nussinov, Ruth
, Woolf, Thomas B.
, Ma, Buyong
, Jang, Hyunbum
in
Amino acids
/ Antimicrobial Cationic Peptides - chemistry
/ Biophysical Theory and Modeling
/ Cells
/ Computer Simulation
/ Effects
/ Lipid Bilayers - chemistry
/ Lipids
/ Membranes
/ Microorganisms
/ Models, Molecular
/ Peptides
/ Peptides - chemistry
/ Phosphatidylcholines - chemistry
/ Phosphatidylglycerols - chemistry
/ Protein Structure, Secondary
/ Proteins - chemistry
/ Thinning
/ Water - chemistry
2006
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Interaction of Protegrin-1 with Lipid Bilayers: Membrane Thinning Effect
by
Nussinov, Ruth
, Woolf, Thomas B.
, Ma, Buyong
, Jang, Hyunbum
in
Amino acids
/ Antimicrobial Cationic Peptides - chemistry
/ Biophysical Theory and Modeling
/ Cells
/ Computer Simulation
/ Effects
/ Lipid Bilayers - chemistry
/ Lipids
/ Membranes
/ Microorganisms
/ Models, Molecular
/ Peptides
/ Peptides - chemistry
/ Phosphatidylcholines - chemistry
/ Phosphatidylglycerols - chemistry
/ Protein Structure, Secondary
/ Proteins - chemistry
/ Thinning
/ Water - chemistry
2006
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Interaction of Protegrin-1 with Lipid Bilayers: Membrane Thinning Effect
Journal Article
Interaction of Protegrin-1 with Lipid Bilayers: Membrane Thinning Effect
2006
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Overview
Protegrins (PG) are important in defending host tissues, preventing infection via an attack on the membrane surface of invading microorganisms. Protegrins have powerful antibiotic abilities, but the molecular-level mechanisms underlying the interactions of their β-sheet motifs with the membrane are not known. Protegrin-1 (PG-1) is composed of 18 amino acids with a high content of basic residues and two disulfide bonds. Here we focused on the stability of PG-1 at the amphipathic interface in lipid bilayers and on the details of the peptide-membrane interactions. We simulated all-atom models of the PG-1 monomer with explicit water and lipid bilayers composed of both homogeneous POPC (palmitoyl-oleyl-phosphatidylcholine) lipids and a mixture of POPC/POPG (palmitoyl-oleyl-phosphatidylglycerol) (4:1) lipids. We observed that local thinning of the lipid bilayers mediated by the peptide is enhanced in the lipid bilayer containing POPG, consistent with experimental results of selective membrane targeting. The β-hairpin motif of PG-1 is conserved in both lipid settings, whereas it is highly bent in aqueous solution. The conformational dynamics of PG-1, especially the highly charged β-hairpin turn region, are found to be mostly responsible for disturbing the membrane. Even though the eventual membrane disruption requires PG-1 oligomers, our simulations clearly show the first step of the monomeric effects. The thinning effects in the bilayer should relate to pore/channel formation in the lipid bilayer and thus be responsible for further defects in the membrane caused by oligomer.
Publisher
Elsevier Inc,Biophysical Society
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