Auer Stefan, Dobson Christopher M, Vendruscolo Michele, Maritan Amos
Centre for Self Organising Molecular Systems, University of Leeds, Leeds LS2 9JT, United Kingdom.
Phys Rev Lett. 2008 Dec 19;101(25):258101. doi: 10.1103/PhysRevLett.101.258101. Epub 2008 Dec 17.
Peptides and proteins exhibit a common tendency to assemble into highly ordered fibrillar aggregates, whose formation proceeds in a nucleation-dependent manner that is often preceded by the formation of oligomeric assemblies. This process has received much attention because disordered oligomeric aggregates have been associated with neurodegenerative disorders such as Alzheimer's and Parkinson's disease. Here we describe a self-templated nucleation mechanism that determines the transition between the initial condensation of polypeptide chains into disordered assemblies and their reordering into fibrillar structures. The results that we present show that at the molecular level this transition is due to the ability of polypeptide chains to reorder within oligomers into fibrillar assemblies whose surfaces act as templates that stabilize the disordered assemblies.
肽和蛋白质表现出组装成高度有序的纤维状聚集体的共同倾向,其形成以成核依赖的方式进行,且通常在寡聚体组装形成之前。由于无序的寡聚聚集体与诸如阿尔茨海默病和帕金森病等神经退行性疾病有关,这一过程受到了广泛关注。在此,我们描述了一种自模板成核机制,该机制决定了多肽链从初始凝聚成无序组装体到重新排列成纤维状结构的转变。我们展示的结果表明,在分子水平上,这种转变是由于多肽链能够在寡聚体内重新排列成纤维状组装体,其表面充当稳定无序组装体的模板。