Steered molecular dynamics studies of the potential of mean force of a Na+ or K+ ion in a cyclic peptide nanotube

被引:74
|
作者
Hwang, Hyonseok [1 ]
Schatz, George C. [1 ]
Ratner, Mark A. [1 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2006年 / 110卷 / 51期
关键词
D O I
10.1021/jp0657888
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Potential of mean force (PMF) profiles of a single Na+ or K+ ion passing through a cyclic peptide nanotube, cyclo[-(D-Ala-Glu-D-Ala-Gln)(2)-], in water are calculated to provide insight into ion transport and to understand the conductance difference between these two ions. The PMF profiles are obtained by performing steered molecular dynamics (SMD) simulations that are based on the Jarzynski equality. The computed PMF profiles for both ions show barriers of around 2.4 kcal/mol at the channel entrances and exits and energy wells in the middle of the tube. The energy barriers, so-called dielectric energy barriers, arise due to the desolvation of water molecules when ions move across the nanotube, and the energy wells appear as a result of attractive interactions between the cations and negatively charged carbonyl oxygens on the backbone of the tube. We find more and deeper energy wells in the PMF profile for Na+ than for K+, which suggests that Na+ ions have a longer residence time inside the nanotube and that permeation of Na+ ions is reduced compared to K+ ions. Calculations of the radial distribution functions (RDF) between the ions and oxygens in the water molecules and in carbonyl groups on the tube and an investigation of the orientations of the carbonyl groups show that, in contrast with the dynamic carbonyl groups observed in the selectivity filter of the KcsA ion channel, the carbonyl groups in the cyclic peptide nanotube are relatively rigid, with only slight reorientation of the carbonyl groups as the cations pass through. The rigidity of the carbonyl groups in the cyclic peptide nanotube can be attributed to their role in hydrogen bonding, which is responsible for the tube structure. Comparison of the PMF profiles with the electrostatic energy profiles calculated from the Poisson-Boltzmann (PB) equation, a dielectric continuum model, reveals that the dielectric continuum model breaks down in the confined region within the tube that governs ion transport.
引用
收藏
页码:26448 / 26460
页数:13
相关论文
共 50 条
  • [21] Swelling of K+, Na+ and Ca2+-montmorillonites and hydration of interlayer cations: a molecular dynamics simulation
    Tao, Liu
    Tian Xiao-Feng
    Yu, Zhao
    Tao, Gao
    CHINESE PHYSICS B, 2010, 19 (10)
  • [22] Unbinding pathway energy of glyphosate from the EPSPs enzyme binding site characterized by Steered Molecular Dynamics and Potential of Mean Force
    Ferreira Junior, Moacir F.
    Franca, Eduardo F.
    Leite, Fabio L.
    JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2017, 72 : 43 - 49
  • [23] Hydration structure of Na+ and K+ from ab initio molecular dynamics based on modern density functional theory
    Bankura, Arindam
    Carnevale, Vincenzo
    Klein, Michael L.
    MOLECULAR PHYSICS, 2014, 112 (9-10) : 1448 - 1456
  • [24] Similarities and differences in interaction of K+ and Na+ with condensed ordered DNA.: A molecular dynamics computer simulation study
    Cheng, YH
    Korolev, N
    Nordenskiöld, L
    NUCLEIC ACIDS RESEARCH, 2006, 34 (02) : 686 - 696
  • [25] The Mechanism of Na+/K+ Selectivity in Mammalian Voltage-Gated Sodium Channels Based on Molecular Dynamics Simulation
    Xia, Mengdie
    Liu, Huihui
    Li, Yang
    Yan, Nieng
    Gong, Haipeng
    BIOPHYSICAL JOURNAL, 2013, 104 (11) : 2401 - 2409
  • [26] Molecular insights into multilayer 18-crown-6-like graphene nanopores for K+/Na+ separation: A molecular dynamics study
    Chen, Yaojia
    Zhu, Yudan
    Ruan, Yang
    Zhao, Nana
    Liu, Wei
    Zhuang, Wei
    Lu, Xiaohua
    CARBON, 2019, 144 : 32 - 42
  • [27] The effect of K+ potential on the nuclear equation of state for the K+ production in heavy ion collisions by using a quantum molecular dynamics model
    Chaimongkon, Phacharatouch
    Jeerakad, Jenitsata
    Doo-saard, Tidarut
    Douykhumklaw, Chanadan
    Prajit, Sakda
    Sittiketkorn, Panadda
    Thongkum, Patcharapan
    Srisawad, Pornrad
    SIAM PHYSICS CONGRESS 2019 (SPC2019): PHYSICS BEYOND DISRUPTION SOCIETY, 2019, 1380
  • [28] Molecular dynamics - potential of mean force calculations as a tool for understanding ion permeation and selectivity in narrow channels
    Allen, Toby W.
    Andersen, Olaf S.
    Roux, Benoit
    BIOPHYSICAL CHEMISTRY, 2006, 124 (03) : 251 - 267
  • [29] NA+-NA+ AND CL--CL- ION-PAIRS IN WATER - MEAN FORCE POTENTIALS BY CONSTRAINED MOLECULAR-DYNAMICS
    GUARDIA, E
    REY, R
    PADRO, JA
    JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (04): : 2823 - 2831
  • [30] The Solvation Structure of Na+ and K+ in Liquid Water Determined from High Level ab Initio Molecular Dynamics Simulations
    Rowley, Christopher N.
    Roux, Benoit
    JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2012, 8 (10) : 3526 - 3535