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\documentclass[prb,aps,twocolumn]{revtex4} |
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\section{\label{sec:DUFF}The DUFF Force Field} |
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\usepackage{amsmath} |
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\usepackage{berkeley} |
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\usepackage{graphicx} |
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\usepackage{tabularx} |
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The DUFF (\underline{D}ipolar \underline{U}nified-atom |
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\underline{F}orce \underline{F}ield) force field was developed to |
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simulate lipid bilayer formation and equilibrium dynamics. We needed a |
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model capable of forming bilaers, while still being sufficiently |
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computationally efficient allowing simulations of large systems |
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(\~100's of phospholipids, \~1000's of waters) for long times (\~10's |
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of nanoseconds). |
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\begin{document} |
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With this goal in mind, we decided to eliminate all charged |
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interactions within the force field. Charge distributions were |
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replaced with dipolar entities, and charge neutral distributions were |
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reduced to Lennard-Jones interaction sites. This simplification cuts |
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the length scale of long range interactions from $\frac{1}{r}$ to |
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$\frac{1}{r^3}$ (Eq.~\ref{eq:dipole} vs.~ Eq.~\ref{eq:coloumb}), |
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allowing us to avoid the computationally expensive Ewald-Sum. Instead, |
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we can use neighbor-lists and cutoff radii for the dipolar |
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interactions. |
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\section{The DUFF Energy Function} |
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\label{sec:energyFunctionals} |
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\begin{align} |
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V^{\text{dipole}}_{ij}(\mathbf{r}_{ij},\boldsymbol{\Omega}_{i}, |
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\boldsymbol{\Omega}_{j}) &= |
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\frac{1}{4\pi\epsilon_{0}} \biggl[ |
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\frac{\boldsymbol{\mu}_{i} \cdot \boldsymbol{\mu}_{j}}{r^{3}_{ij}} |
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- |
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\frac{3(\boldsymbol{\mu}_i \cdot \mathbf{r}_{ij}) % |
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(\boldsymbol{\mu}_j \cdot \mathbf{r}_{ij}) } |
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{r^{5}_{ij}} \biggr]\label{eq:dipole} \\ |
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V^{\text{ch}}_{ij}(\mathbf{r}_{ij}) &= \frac{q_{i}q_{j}}% |
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{4\pi\epsilon_{0} r_{ij}} \label{eq:coloumb} |
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\end{align} |
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Applying this standard to the lipid model, we decided to represent the |
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lipid model as a point dipole interaction site. Lipid head groups are |
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typically zwitterionic in nature, with sometimes full integer charges |
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seperated by only 5 to 6~$\mbox{\AA}$. By placing a dipole of |
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20.6~Debye at the head groups center of mass, our model mimics the |
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dipole of DMPC.\cite{Cevc87} Then, to account for the steric henderanc |
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of the head group, a Lennard-Jones interaction site is also oacted at |
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the psuedoatom's center of mass. The model is illustrated in |
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Fig.~\ref{fig:lipidModel}. |
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\begin{figure} |
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\includegraphics[angle=-90,width=\linewidth]{lipidModel.epsi} |
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\caption{A representation of the lipid model. $\phi$ is the torsion angle, $\theta$ % |
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is the bend angle, $\mu$ is the dipole moment of the head group, and n is the chain length.} |
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\label{fig:lipidModel} |
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\end{figure} |
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The main energy function in OOPSE is DUFF (the Dipolar |
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Unified-atom Force Field). DUFF is a collection of parameters taken |
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from Seipmann \emph{et al.}\cite{Siepmann1998} and Ichiye \emph{et |
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Turning to the tail chains of the phospholipids, we needed a set of |
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scalable parameters to model the alkyl groups as Lennard-Jones |
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interaction sites. For this, we used the TraPPE force field of |
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Siepmann \emph{et al}.\cite{Siepmann1998} The force field is a |
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unified-atom representation of n-alkanes. It is parametrized against |
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phase equilibria using Gibbs Monte Carlo simulation techniques. One of |
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the advantages of TraPPE is that is generalizes the types of atoms in |
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an alkyl chain to keep the number of pseudoatoms to a minimum. |
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%( $ \mbox{CH_3} $ %-$\mathbf{\mbox{CH_2}}$-$\mbox{CH_3}$ is the same as |
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Another advantage of using TraPPE is the constraining of all bonds to |
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be of fixed length. Typically, bond vibrations are the motions in a |
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molecular dynamic simulation. This neccesitates a small time step |
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between force evaluations be used to ensure adequate sampling of the |
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bond potential. Failure to do so will result in loss of energy |
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conservation within the microcanonical ensemble. By constraining this |
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degree of freedom, time steps larger than were previously allowable |
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are able to be used when integrating the equations of motion. |
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|
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The main energy function in OOPSE is DUFF (the Dipolar Unified-atom |
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Force Field). DUFF is a collection of parameters taken from Seipmann |
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and Ichiye \emph{et |
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al.}\cite{liu96:new_model} The total energy of interaction is given by |
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Eq.~\ref{eq:totalPotential}: |
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\begin{equation} |
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\end{equation} |
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– |
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\bibliography{oopse} |
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\end{document} |
