A'/> A comparative study of hydrogen bonding structure and dynamics in aqueous urea solution of amides with varying hydrophobicity: Effect of addition of trimethylamine <ce:italic>N</ce:italic>-oxide (TMAO)
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A comparative study of hydrogen bonding structure and dynamics in aqueous urea solution of amides with varying hydrophobicity: Effect of addition of trimethylamine N-oxide (TMAO)

机译:不同疏水性含水尿素水溶液中氢粘接结构和动力学的对比研究:三甲胺的添加效果 n - 氧化物(Tmao)

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Abstract A comparison of effects of addition of TMAO on the hydrogen bonding structure and dynamics in aqueous urea solution of three different amides (formamide-FA, N-methylformamide-NMF, N-methylacetamide-NMA), have been carried out with the help of classical molecular dynamics simulations. The interactions between amide-water, amide-urea and amide-TMAO in presence of concentrated urea/urea-TMAO solution are depicted here by different site-site radial distribution functions and the average interaction energies between these species in the solution. It is observed that the aqueous peptide hydrogen bond interaction is preferably stronger with increasing TMAO concentration in the solution, particularly for NMF and NMA, where hydrophobic solvation of CH3-groups increases significantly in TMAO solution. Upon increasing the size of hydrophobic groups of NMA, hydrogen bonding capacity decreases while interaction of hydrophobic groups with TMAO is seen to be favourable. The lifetimes of amide-water, water-water hydrogen bonds are found to increase with TMAO concentration in the solution. While all FA-water hydrogen bonds exhibit faster dynamics and reduced lifetimes, HNMF OWAT hydrogen bonding is most persistent in terms of lifetime but shows faster reorganisation than that of NMA-water hydrogen bonds. Our calculated self-diffusion coefficients and orientational relaxation times shows slower dynamics of amide, water as well as solute molecules owing to strong inter-species hydrogen bonding at elevated TMAO concentrations. Graphical abstract Display Omitted Highlights ? Amide-urea interactions decrease in presence of TMAO, except in case of FA. ? Aqueous solvation of hydrophobic groups more enhanced in TMAO than in urea solution ? Faster dynamics in FA-water hydrogen bonds compared to NMF/NMA-water ? HNMF OWAT hydrogen bonds have highest lifetime and reorganise
机译:<![cdata [ 抽象 在三种不同酰胺水溶液溶液中添加TMAO对氢键结构和动力学的影响的比较(Formamide-Fa, n - 甲基甲酰胺-nmf, n - 甲基乙酰胺-nma),并在古典分子的帮助下进行动态模拟。通过不同的位点位点径向分布功能和这些物种在溶液中的平均相互作用能量,在此处描述酰胺 - 水,酰胺 - 尿素和酰胺-TMAO之间的相互作用。观察到含水肽氢键相互作用优选较强,随着溶液中的TMAO浓度增加,特别是对于NMF和NMA,其中CH 3 的疏水溶剂,组在TMAO解决方案中显着增加。在增加NMA疏水基团的尺寸后,氢键能力降低,同时疏水基团与TMAO的相互作用被观察到有利。酰胺水,水 - 水氢键的寿命随溶液中的TMAO浓度而增加。虽然所有FA水氢键具有更快的动态和减少的生命,但H NMF ... O WAT 氢键在寿命方面最持久,但显示比NMA水氢键更快的重组。我们计算的自扩散系数和取向松弛时间显示酰胺,水以及由于在升高的TMAO浓度下的较强的物种间氢键合的较慢的酰胺和溶质分子。 图形抽象 显示省略 亮点 amide-utea交互在tmao存在下减少,除了在FA。 疏水组的水溶液在tmao中更具增强,而不是尿素溶液 h NMF ... O WAT 氢键有最高的寿命并重新组织

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