Wymore T, Wong T C
Department of Chemistry, University of Missouri, Columbia, Missouri 65211 USA.
Biophys J. 1999 Mar;76(3):1213-27. doi: 10.1016/S0006-3495(99)77285-1.
Two neuropeptides, substance P (SP) and SP-tyrosine-8 (SP-Y8), have been studied by molecular dynamics (MD) simulation in an explicit sodium dodecylsulfate (SDS) micelle. Initially, distance restraints derived from NMR nuclear Overhauser enhancements (NOE) were incorporated in the restrained MD (RMD) during the equilibration stage of the simulation. It was shown that when SP-Y8 was initially placed in an insertion (perpendicular) configuration, the peptide equilibrated to a surface-bound (parallel) configuration in approximately 450 ps. After equilibration, the conformation and orientation of the peptides, the solvation of both the backbone and the side chain of the residues, hydrogen bonding, and the dynamics of the peptides were analyzed from trajectories obtained from the RMD or the subsequent free MD (where the NOE restraints were removed). These analyses showed that the peptide backbones of all residues are either solvated by water or are hydrogen-bonded. This is seen to be an important factor against the insertion mode of interaction. Most of the interactions come from the hydrophobic interaction between the side chains of Lys-3, Pro-4, Phe-7, Phe-8, Leu-10, and Met-11 for SP, from Lys-3, Phe-7, Leu-10, and Met-11 in SP-Y8, and the micellar interior. Significant interactions, electrostatic and hydrogen bonding, between the N-terminal residues, Arg-Pro-Lys, and the micellar headgroups were observed. These latter interactions served to affect both the structure and, especially, the flexibility, of the N-terminus. The results from simulation of the same peptides in a water/CCl4 biphasic cell were compared with the results of the present study, and the validity of using the biphasic system as an approximation for peptide-micelle or peptide-bilayer systems is discussed.
通过分子动力学(MD)模拟,在明确的十二烷基硫酸钠(SDS)胶束中研究了两种神经肽,即P物质(SP)和SP-酪氨酸-8(SP-Y8)。最初,在模拟的平衡阶段,将源自核磁共振核Overhauser增强(NOE)的距离约束纳入受限MD(RMD)中。结果表明,当SP-Y8最初以插入(垂直)构型放置时,该肽在约450皮秒内平衡为表面结合(平行)构型。平衡后,从RMD或随后的自由MD(去除了NOE约束)获得的轨迹分析了肽的构象和取向、残基主链和侧链的溶剂化、氢键以及肽的动力学。这些分析表明,所有残基的肽主链要么被水溶剂化,要么形成氢键。这被视为不利于插入相互作用模式的一个重要因素。对于SP,大多数相互作用来自Lys-3、Pro-4、Phe-7、Phe-8、Leu-10和Met-11侧链之间的疏水相互作用,对于SP-Y8,来自Lys-3、Phe-7、Leu-10和Met-11,以及胶束内部。在N端残基Arg-Pro-Lys和胶束头部基团之间观察到显著的静电和氢键相互作用。后一种相互作用既影响结构,特别是N端的柔韧性。将相同肽在水/CCl4双相细胞中的模拟结果与本研究结果进行了比较,并讨论了使用双相系统作为肽-胶束或肽-双层系统近似的有效性。