Binding of Different Cyclosporin Variants to Micelles Evidenced by NMR and MD Simulations.
Polina P KobchikovaSergey V EfimovVladimir V KlochkovPublished in: Membranes (2023)
Peptides play a critical role in the life of organisms, performing completely different functions. The biological activity of some peptides, such as cyclosporins, can be determined by the degree of membrane permeability. Thus, it becomes important to study how the molecule interacts with lipid bilayers. Cyclosporins C, E, H and L were characterised molecular dynamics simulation; NMR spectroscopy studies were also carried out for cyclosporins C and E. The comparison of one- and two-dimensional spectra revealed certain similarities between spatial structures of the studied cyclosporin variants. Upon dissolving in water containing DPC micelles, which serve as model membranes, subtle changes in the NMR spectra appear, but in a different way for different cyclosporins. In order to understand whether observed changes are related to any structural modifications, simulation of the interaction of the peptide with the phospholipid micelle was performed. The onset of the interaction was observed, when the peptide is trapped to the surface of the micelle. Simulations of this kind are also of interest in the light of the well-known membrane permeability of cyclosporin, which is important for its biological action.
Keyphrases
- molecular dynamics simulations
- molecular dynamics
- high resolution
- solid state
- drug delivery
- magnetic resonance
- density functional theory
- copy number
- molecular docking
- drug release
- cancer therapy
- endothelial cells
- fatty acid
- amino acid
- monte carlo
- binding protein
- hyaluronic acid
- gram negative
- mass spectrometry
- gene expression
- multidrug resistant
- dna binding
- transcription factor