4.7 Article

Second-order Poisson-Nernst-Planck solver for ion transport

期刊

JOURNAL OF COMPUTATIONAL PHYSICS
卷 230, 期 13, 页码 5239-5262

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcp.2011.03.020

关键词

Ion channels; Poisson-Nernst-Planck equations; Matched interface and boundary; Dirichlet to Neumann mapping; Gramicidin A

资金

  1. NSF [CCF-0936830]
  2. NIH [R01GM-090208]
  3. MSU [91-4600]
  4. Direct For Computer & Info Scie & Enginr
  5. Division of Computing and Communication Foundations [0936830] Funding Source: National Science Foundation

向作者/读者索取更多资源

The Poisson-Nernst-Planck (PNP) theory is a simplified continuum model for a wide variety of chemical, physical and biological applications. Its ability of providing quantitative explanation and increasingly qualitative predictions of experimental measurements has earned itself much recognition in the research community. Numerous computational algorithms have been constructed for the solution of the PNP equations. However, in the realistic ion-channel context, no second-order convergent PNP algorithm has ever been reported in the literature, due to many numerical obstacles, including discontinuous coefficients, singular charges, geometric singularities, and nonlinear couplings. The present work introduces a number of numerical algorithms to overcome the abovementioned numerical challenges and constructs the first second-order convergent PNP solver in the ion-channel context. First, a Dirichlet to Neumann mapping (DNM) algorithm is designed to alleviate the charge singularity due to the protein structure. Additionally, the matched interface and boundary (MIB) method is reformulated for solving the PNP equations. The MIB method systematically enforces the interface jump conditions and achieves the second order accuracy in the presence of complex geometry and geometric singularities of molecular surfaces. Moreover, two iterative schemes are utilized to deal with the coupled nonlinear equations. Furthermore, extensive and rigorous numerical validations are carried out over a number of geometries, including a sphere, two proteins and an ion channel, to examine the numerical accuracy and convergence order of the present numerical algorithms. Finally, application is considered to a real transmembrane protein, the Gramicidin A channel protein. The performance of the proposed numerical techniques is tested against a number of factors, including mesh sizes, diffusion coefficient profiles, iterative schemes, ion concentrations, and applied voltages. Numerical predictions are compared with experimental measurements. (C) 2011 Elsevier Inc. All rights reserved.

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