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- W2736423475 abstract "Understanding how different classes of molecules move across biological membranes is a prerequisite to predicting a solute’s permeation rate, which is a critical factor in the fields of drug design and pharmacology. We use biased molecular dynamics computer simulations to calculate and compare the free energy profiles of translocation of several small molecules across 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) lipid bilayers as a first step toward determining the most efficient method for free energy calculations. We study the translocation of arginine, a sodium ion, alanine, and a single water molecule using the metadynamics, umbrella sampling, and replica exchange umbrella sampling techniques. Within the fixed lengths of our simulations, we find that all methods produce similar results for charge-neutral permeants, but not for polar or positively charged molecules. We identify the long relaxation time scale of electrostatic interactions between lipid headgroups and the solute to be the principal cause of this difference and show that this slow process can lead to an erroneous dependence of computed free energy profiles on the initial system configuration. We demonstrate the use of committor analysis to validate the proper sampling of the presumed transition state, which in our simulations is achieved only in replica exchange calculations. On the basis of these results we provide some useful guidance to perform and evaluate free energy calculations of membrane permeation." @default.
- W2736423475 created "2017-07-31" @default.
- W2736423475 creator A5002248940 @default.
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- W2736423475 date "2018-02-06" @default.
- W2736423475 modified "2023-10-14" @default.
- W2736423475 title "Free Energy Calculations of Membrane Permeation: Challenges Due to Strong Headgroup–Solute Interactions" @default.
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- W2736423475 doi "https://doi.org/10.1021/acs.jctc.7b01159" @default.
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