Motion of a cylindrical dielectric boundary

Li Tien Cheng, Bo Li, Michael White, Shenggao Zhou

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

The interplay between geometry and electrostatics contributes significantly to hydrophobic interactions of biomolecules in an aqueous solution. With an implicit solvent, such a system can be described macroscopically by the dielectric boundary that separates the high-dielectric solvent from low-dielectric solutes. This work concerns the motion of a model cylindrical dielectric boundary as the steepest descent of a free-energy functional that consists of both the surface and electrostatic energies. The effective dielectric boundary force is defined, and an explicit formula of the force is obtained. It is found that such a force always points from the solvent region to the solute region. In the case that the interior of a cylinder is of a lower dielectric, the motion of the dielectric boundary is initially driven dominantly by the surface force but is then driven inward quickly to the cylindrical axis by both the surface and electrostatic forces. In the case that the interior of a cylinder is of a higher dielectric, the competition between the geometrical and electrostatic contributions leads to the existence of equilibrium boundaries that are circular cylinders. Linear stability analysis is presented to show that such an equilibrium is only stable for a perturbation with a wavenumber larger than a critical value. Numerical simulations are reported for both of the cases, confirming the analysis on the role of each component of the driving force. Implications of the mathematical findings to the understanding of charged molecular systems are discussed.

Original languageEnglish (US)
Pages (from-to)594-616
Number of pages23
JournalSIAM Journal on Applied Mathematics
Volume73
Issue number1
DOIs
StatePublished - 2013

Keywords

  • Charged molecules
  • Dielectric boundaries
  • Effective dielectric boundary force
  • Electrostatic energy
  • Linear stability
  • Surface energy

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