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环状肽纳米管中Na⁺或K⁺离子平均力势的引导分子动力学研究。

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

作者信息

Hwang Hyonseok, Schatz George C, Ratner Mark A

机构信息

Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA.

出版信息

J Phys Chem B. 2006 Dec 28;110(51):26448-60. doi: 10.1021/jp0657888.

Abstract

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.

摘要

计算了单个Na⁺或K⁺离子通过环状肽纳米管环[-(D-丙氨酸-谷氨酸-D-丙氨酸-谷氨酰胺)₂-]在水中的平均力势(PMF)分布,以深入了解离子传输并理解这两种离子之间的电导差异。通过基于雅尔津斯基等式进行的引导分子动力学(SMD)模拟获得PMF分布。两种离子的计算PMF分布在通道入口和出口处显示约2.4千卡/摩尔的势垒,在管中部有能量阱。这些能量势垒,即所谓的介电能垒,是由于离子穿过纳米管时水分子的去溶剂化而产生的,而能量阱是阳离子与管主链上带负电荷的羰基氧之间的吸引相互作用的结果。我们发现Na⁺的PMF分布中的能量阱比K⁺的更多更深,这表明Na⁺离子在纳米管内的停留时间更长,并且与K⁺离子相比,Na⁺离子的渗透减少。计算离子与水分子中的氧以及管上羰基中的氧之间的径向分布函数(RDF),并研究羰基的取向,结果表明,与在KcsA离子通道的选择性过滤器中观察到的动态羰基不同,环状肽纳米管中的羰基相对刚性,当阳离子通过时羰基只有轻微的重新取向。环状肽纳米管中羰基的刚性可归因于它们在氢键形成中的作用,氢键形成负责管的结构。将PMF分布与从泊松-玻尔兹曼(PB)方程(一种介电连续介质模型)计算的静电能分布进行比较,结果表明介电连续介质模型在控制离子传输的管内受限区域中失效。

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