ArticlePLoS computational biology2009
Poisson-Nernst-Planck models of nonequilibrium ion electrodiffusion through a protegrin transmembrane pore.
Article in PLoS computational biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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19 citing papers in PubMed, 51 citations in OpenAlex.
- Sensitivity analysis of the Poisson Nernst-Planck equations: a finite element approximation for the sensitive analysis of an electrodiffusion model.Journal of mathematical biology · 2019Article
- Multiscale Models of Antibiotic Probiotics.Current opinion in chemical engineering · 2014Article
- Protein arcs may form stable pores in lipid membranes.Biophysical journal · 2014Article
- Article
- A Stabilized Finite Element Method for Modified Poisson-Nernst-Planck Equations to Determine Ion Flow Through a Nanopore.Communications in computational physics · 2014Article
- Membrane interactions and pore formation by the antimicrobial peptide protegrin.Biophysical journal · 2013Article
- Collective diffusion model for ion conduction through microscopic channels.Biophysical journal · 2013Article
- Modeling and simulation of ion channels.Chemical reviews · 2012Review
- Multiscale models of the antimicrobial peptide protegrin-1 on gram-negative bacteria membranes.International journal of molecular sciences · 2012Review
- Thermodynamic analysis of protegrin-1 insertion and permeation through a lipid bilayer.The journal of physical chemistry. B · 2011Article
- A theory for the proton transport of the influenza virus M2 protein: extensive test against conductance data.Biophysical journal · 2011Article
- Testing the applicability of Nernst-Planck theory in ion channels: comparisons with Brownian dynamics simulations.PloS one · 2011Article
- Review
- Poisson-Nernst-Planck Equations for Simulating Biomolecular Diffusion-Reaction Processes I: Finite Element Solutions.Journal of computational physics · 2010Article
- Dimerization of protegrin-1 in different environments.International journal of molecular sciences · 2010Article
- Free energy profile of the interaction between a monomer or a dimer of protegrin-1 in a specific binding orientation and a model lipid bilayer.The journal of physical chemistry. B · 2010Article
- Antimicrobial mechanism of pore-forming protegrin peptides: 100 pores to kill E. coli.Peptides · 2010Article
- Relative free energy of binding between antimicrobial peptides and SDS or DPC micelles.Molecular simulation · 2009Article
- Mechanisms of antimicrobial, cytolytic, and cell-penetrating peptides: from kinetics to thermodynamics.Biochemistry · 2009Article
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4 authors at 1 institution in 1 country.
Funding
Abstract
Protegrin peptides are potent antimicrobial agents believed to act against a variety of pathogens by forming nonselective transmembrane pores in the bacterial cell membrane. We have employed 3D Poisson-Nernst-Planck (PNP) calculations to determine the steady-state ion conduction characteristics of such pores at applied voltages in the range of -100 to +100 mV in 0.1 M KCl bath solutions. We have tested a variety of pore structures extracted from molecular dynamics (MD) simulations based on an experimentally proposed octomeric pore structure. The computed single-channel conductance values were in the range of 290-680 pS. Better agreement with the experimental range of 40-360 pS was obtained using structures from the last 40 ns of the MD simulation, where conductance values range from 280 to 430 pS. We observed no significant variation of the conductance with applied voltage in any of the structures that we tested, suggesting that the voltage dependence observed experimentally is a result of voltage-dependent channel formation rather than an inherent feature of the open pore structure. We have found the pore to be highly selective for anions, with anionic to cationic current ratios (I(Cl-)/I(K+)) on the order of 10(3). This is consistent with the highly cationic nature of the pore but surprisingly in disagreement with the experimental finding of only slight anionic selectivity. We have additionally tested the sensitivity of our PNP model to several parameters and found the ion diffusion coefficients to have a significant influence on conductance characteristics. The best agreement with experimental data was obtained using a diffusion coefficient for each ion set to 10% of the bulk literature value everywhere inside the channel, a scaling used by several other studies employing PNP calculations. Overall, this work presents a useful link between previous work focused on the structure of protegrin pores and experimental efforts aimed at investigating their conductance characteristics.
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