Molecular Dynamics Investigation of Lipid-Specific Interactions with a Fusion Peptide.
William T HellerPublished in: Biomolecules (2024)
The HIV-1 fusion peptide, which is a short hydrophobic peptide from the gp41 coat glycoprotein that participates in the infection of a cell, interacts with model lipid bilayer membranes in a concentration-dependent manner. The interaction of the peptide with the bilayer also strongly depends on the lipid composition. Here, molecular dynamics simulations were performed to investigate lipid-specific interactions that arise shortly after the binding of a less-fusogenic variant of the HIV-1 fusion peptide to a lipid bilayer composed of a mixture of dimyristoyl phosphatidylcholine and dimyristoyl phosphatidylglycerol. The impact of peptide concentration was also studied. An improved understanding was gained of the lipid-specific interactions experienced by the FP. New insight was also gained into how the peptide concentration changes these interactions.
Keyphrases
- molecular dynamics
- molecular dynamics simulations
- fatty acid
- antiretroviral therapy
- hiv infected
- human immunodeficiency virus
- hepatitis c virus
- hiv positive
- stem cells
- hiv testing
- mesenchymal stem cells
- density functional theory
- transcription factor
- molecular docking
- binding protein
- cell therapy
- dna binding
- ionic liquid