Wu Chun, Lei Hongxing, Duan Yong
Genome Center and Department of Applied Science, University of California, Davis, California 95616, USA.
Biophys J. 2005 Apr;88(4):2897-906. doi: 10.1529/biophysj.104.055574. Epub 2005 Jan 14.
We observed fast aggregation of partially ordered oligomers in an earlier simulation study of an amyloidogenic hexapeptide NFGAIL. In this work, the nucleation of highly ordered oligomers was further investigated by a combined total of 960 ns molecular dynamics simulations with explicit solvent on NFGAIL and its nonamyloidogenic mutant NAGAIL. In these simulations, four dimer subunits that each was constrained by harmonic forces as a two-strand beta-sheet were used to enhance the rate of formation. It was found that a critical role played by the aromatic residue Phe was to direct the stacking of beta-sheets to form ordered multilayer aggregates. We also found that many molecular arrangements of the peptide satisfied the "cross-beta-structure", a hallmark of amyloid fibrils. The tendency for the peptide to form either parallel or antiparallel beta-sheet was comparable, as was the tendency for the beta-sheets to stack either in parallel or antiparallel orientation. Overall, approximately 85% of the native hexapeptide formed octamers. The fact that only 8% of the octamers were well-ordered species suggests that the dissociation of the disordered oligomers be the rate-limiting step in the formation of highly ordered oligomers. Among the well-ordered subunit pairs, about half was formed by the beta-sheet extension along the main-chain hydrogen-bond direction, whereas the other half was formed by the beta-sheet stacking. Hence, a delicate balance between intersheet and intrasheet interactions appeared to be crucial in the formation of a highly ordered nucleus of amyloid fibrils. The disordered oligomers were mainly stabilized by nonspecific hydrophobic interactions, whereas the well-ordered oligomers were further stabilized by cross-strand hydrogen bonds and favorable side-chain stacking.
在早期对淀粉样六肽NFGAIL的模拟研究中,我们观察到部分有序低聚物的快速聚集。在这项工作中,通过对NFGAIL及其非淀粉样生成突变体NAGAIL进行总共960纳秒的显式溶剂分子动力学模拟,进一步研究了高度有序低聚物的成核过程。在这些模拟中,使用四个二聚体亚基,每个亚基通过谐和力作为双链β-折叠进行约束,以提高形成速率。研究发现,芳香族残基苯丙氨酸发挥的关键作用是引导β-折叠的堆积以形成有序的多层聚集体。我们还发现,该肽的许多分子排列满足“交叉β-结构”,这是淀粉样纤维的一个标志。该肽形成平行或反平行β-折叠的趋势相当,β-折叠以平行或反平行方向堆积的趋势也相当。总体而言,约85%的天然六肽形成了八聚体。只有8%的八聚体是有序物种这一事实表明,无序低聚物的解离是形成高度有序低聚物的限速步骤。在有序的亚基对中,约一半是由β-折叠沿主链氢键方向延伸形成的,而另一半是由β-折叠堆积形成的。因此,片层间和片层内相互作用之间的微妙平衡似乎对淀粉样纤维高度有序核的形成至关重要。无序低聚物主要通过非特异性疏水相互作用稳定,而有序低聚物则通过跨链氢键和有利的侧链堆积进一步稳定。