Balance of Solvent and Chain Interactions Determines the Local Stress State of Simulated Membranes
- 15 July 2020
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 124 (32), 6963-6971
- https://doi.org/10.1021/acs.jpcb.0c03937
Abstract
Characterization of the internal mechanical state of model lipid membranes is essential to understand the microscopic underpinnings of biological functions such as membrane fission and organelle shaping within the context of elastic theories such as the Helfrich framework. Here, we compute lateral stress or pressure profiles from molecular dynamics simulations of lipid bilayers and water-vacuum interfaces to understand the role that solvent treatment and force-field parametrization plays on the local mechanical features of membranes. We focus on two atomistic models, GROMOS 43A1-S3 and CHARMM36, and several variants of the MARTINI coarse-grained force-field, including the single-bead non-polar water, three-point polarizable water, big multipole water, and solvent-free. Our results show that the various atomistic and coarse-grained force-fields produce contrasting lateral stress profiles as a result of the balance of solvent-solvent and solvent-solute forces at the hydrocarbon-water interface and fundamentally different treatment of pairwise (e.g., van der Waals, Coulomb, etc.) and multi-body interactions (angles and torsions). Numerical integration of the second moment of the bilayer stress profiles indicates that different local distributions of repulsive and attractive stresses across the membrane, due to distinct force-field parametrizations, may result in substantial variations in macroscopic elastic properties.Keywords
Funding Information
- Division of Chemistry (CHE-1944892)
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