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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Steered Molecular Dynamics Studies of the Potential of Mean Force of a Na~+ or K~+ Ion in a Cyclic Peptide Nanotube
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Steered Molecular Dynamics Studies of the Potential of Mean Force of a Na~+ or K~+ Ion in a Cyclic Peptide Nanotube

机译:环状肽纳米管中Na〜+或K〜+离子的平均力势的定向分子动力学研究

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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.
机译:计算了单个Na〜+或K〜+离子在水中穿过环状肽纳米管cyclo [-((D-Ala-Glu-D-Ala-Gln)_2-]的平均力(PMF)分布的潜力通过深入了解Jarzynski等式,进行分子导向动力学(SMD)模拟,获得了PMF分布图。在通道入口和出口处以及管中部的能量阱处为2.4 kcal / mol。由于离子在纳米管上移动时水分子的去溶剂化作用,能量势垒(所谓的介电能量势垒)升高出现是由于阳离子与管骨架上带负电荷的羰基氧之间有吸引力的相互作用所致。我们在PMF谱中发现Na〜+的能量阱比K〜+的能量阱更深,这表明Na〜+离子在纳米内有更长的停留时间与K〜+离子相比,Na〜+离子的渗透率降低了。计算水分子和羰基上离子和氧之间的径向分布函数(RDF)并研究羰基表明,与在KcsA离子通道的选择性过滤器中观察到的动态羰基相反,环状肽纳米管中的羰基相对较硬,随着阳离子的穿过,羰基仅略微重新取向。环状肽纳米管中羰基的刚性可以归因于它们在氢键中的作用,氢负责管的结构。将PMF曲线与通过Poisson-Boltzmann(PB)方程计算得出的静电能曲线进行比较,介电连续模型,表明介电连续模型在控制离子传输的管子内的受限区域中破裂。

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