Accurate Binding of Sodium and Calcium to a POPC Bilayer by Effective Inclusion of Electronic Polarization
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Electricity MeSH
- Phosphatidylcholines chemistry MeSH
- Lipid Bilayers chemistry MeSH
- Molecular Dynamics Simulation MeSH
- Sodium chemistry MeSH
- Calcium chemistry MeSH
- Binding Sites MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 1-palmitoyl-2-oleoylphosphatidylcholine MeSH Browser
- Phosphatidylcholines MeSH
- Lipid Bilayers MeSH
- Sodium MeSH
- Calcium MeSH
Binding affinities and stoichiometries of Na+ and Ca2+ ions to phospholipid bilayers are of paramount significance in the properties and functionality of cellular membranes. Current estimates of binding affinities and stoichiometries of cations are, however, inconsistent due to limitations in the available experimental and computational methods. In this work, we improve the description of the binding details of Na+ and Ca2+ ions to a 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) bilayer by implicitly including electronic polarization as a mean field correction, known as the electronic continuum correction (ECC). This is applied by scaling the partial charges of a selected state-of-the-art POPC lipid model for molecular dynamics simulations. Our improved ECC-POPC model reproduces not only the experimentally measured structural parameters for the ion-free membrane, but also the response of lipid headgroup to a strongly bound cationic amphiphile, as well as the binding affinities of Na+ and Ca2+ ions. With our new model, we observe on the one side negligible binding of Na+ ions to POPC bilayer, while on the other side stronger interactions of Ca2+ primarily with phosphate oxygens, which is in agreement with the previous interpretations of the experimental spectroscopic data. The present model results in Ca2+ ions forming complexes with one to three POPC molecules with almost equal probabilities, suggesting more complex binding stoichiometries than those from simple models used to interpret the NMR data previously. The results of this work pave the way to quantitative molecular simulations with realistic electrostatic interactions of complex biochemical systems at cellular membranes.
Department of Physical Chemistry Institute of Chemical Technology 166 28 Prague 6 Czech Republic
Department of Physics Tampere University of Technology P O Box 692 FI 33101 Tampere Finland
Institute of Biotechnology University of Helsinki 00100 Helsinki Finland
References provided by Crossref.org
Curvature Matters: Modeling Calcium Binding to Neutral and Anionic Phospholipid Bilayers
Accurate Simulations of Lipid Monolayers Require a Water Model with Correct Surface Tension