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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Examination of Trifluoroethanol Interactions with Trp-Cage in Trifluoroethanol-Water at 298 K through Molecular Dynamics Simulations and Intermolecular Nuclear Overhauser Effects
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Examination of Trifluoroethanol Interactions with Trp-Cage in Trifluoroethanol-Water at 298 K through Molecular Dynamics Simulations and Intermolecular Nuclear Overhauser Effects

机译:通过分子动力学模拟和分子间核传承效应检查三氟乙醇 - 水中三氟乙醇 - 水中三氟乙醇与三氟乙醇 - 水相互作用

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摘要

Molecular dynamics simulations of the protein model Trp-cage in 42% trifluoroethanol (TFE)-water at 298 K have been carried out with the goal of exploring peptide hydrogen-solvent fluorine nuclear spin cross-relaxation. The TFES model of TFE developed in a previous work was used with the TIPSP-Ew model of water. System densities and component translational diffusion coefficients predicted by the simulations were within 20% of the experimental values. Consideration of the calculated relative amounts of TFE and water surrounding the hydrogens of Trp-cage indicated that the composition of the solvent mixture beyond similar to 1.5 nm from the van der Waals surface of the peptide is close to the composition of the bulk solvent, but as observed by others, TFE accumulates preferentially near the peptide surface. In the simulations, both TFE and water molecules make contacts with the peptide surface; water molecules predominate in contacts with the peptide backbone atoms and TFE molecules generally preferentially interact with side chains. Translational diffusion of solvent molecules appears to be slowed near the surface of the peptide. Depending on the location in the structure, TFE molecules form complexes with the peptide that may persist for up to similar to 7 ns. Many of the peptide spin-solvent fluorine cross-relaxation parameters (Sigma(HF)) for which experimental values are available are reasonably well-predicted from the simulations. However, the calculated Sigma(HF) values were too small for some hydrogens of the 6Trp indole ring and the amino acid hydrogens near this residue in the native structure, whereas Sigma(HF) values for hydrogens on the side chains of 1Asn, 4Ile, and 7Leu are too large. In 42% TFE-water, persistent conformations of Trp-cage are found, which differ from the conformation found in water by the orientation of the 3Tyr ring.
机译:通过探索肽氢 - 溶剂氟核旋转交叉弛豫的目的,进行了42%三氟乙醇(TFE)-WATER中蛋白质模型Trp-笼中的分子动力学模拟。在以前的工作中开发的TFE的TFES模型与水的TIPSP-EW模型一起使用。通过模拟预测的系统密度和组分平移扩散系数在实验值的20%以内。考虑到TRP-笼的液体周围的TFE和水的计算相对量表明,溶剂混合物的组成超过类似于1.5nm的肽,肽的van der WaaS表面接近散装溶剂的组成,但是如其他人所观察到的,TFE优先在肽表面附近累积。在模拟中,TFE和水分子都与肽表面接触;水分子占主导地位与肽骨架原子和TFE分子的接触,通常优先与侧链相互作用。溶剂分子的平移扩散似乎在肽表面附近变慢。根据结构中的位置,TFE分子与可能持续到类似于7ns的肽形成复合物。许多肽旋转溶剂氟易弛豫参数(Sigma(HF))可获得实验值的可用性可获得的实验值。然而,计算出的Sigma(HF)值对于6TRP吲哚环的一些氢和在本地结构附近该残基附近的氨基酸液体,而1ASN,4侧链的含氢的Sigma(HF)值。和7Leu太大了。在42%的TFE水中,发现TRP-COGE的持续构象,其与水在水中发现的构象不同,通过3TYR环的取向不同。

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