Coarse-grained model of titrating peptides interacting with lipid bilayers

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Bibtex

@article{3083ab2bed2542f7a2b34e7948ee3685,
title = "Coarse-grained model of titrating peptides interacting with lipid bilayers",
abstract = "Molecular-level computer simulations of peptide aggregation, translocation, and protonation at and in biomembranes are impeded by the large time and length scales involved. We present a computationally efficient, coarse-grained, and solvent-free model for the interaction between lipid bilayers and peptides. The model combines an accurate description of mechanical membrane properties with a new granular representation of the dielectric mismatch between lipids and the aqueous phase. All-atom force fields can be easily mapped onto the coarse-grained model, and parameters for coarse-grained monopeptides accurately extrapolate to membrane permeation free energies for the corresponding dipeptides and tripeptides. Acid-base equilibria of titratable amino acid residues are further studied using a constant-pH ensemble, capturing protonation state changes upon membrane translocation. Important differences between histidine, lysine, and arginine are observed, which are in good agreement with experimental observations.",
author = "Giulio Tesei and Mario Vazdar and Mikael Lund",
year = "2018",
doi = "10.1063/1.5058234",
language = "English",
volume = "149",
journal = "Journal of Chemical Physics",
issn = "0021-9606",
publisher = "American Institute of Physics",
number = "24",

}