Rudolph Stephan, Klein Antonia Nicole, Tusche Markus, Schlosser Christine, Elfgen Anne, Brener Oleksandr, Teunissen Charlotte, Gremer Lothar, Funke Susanne Aileen, Kutzsche Janine, Willbold Dieter
Institute of Complex Systems, Structural Biochemistry (ICS-6), Research Centre Jülich, 52425 Jülich, Germany.
Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, 40225 Düsseldorf, Germany.
PLoS One. 2016 Feb 3;11(2):e0147470. doi: 10.1371/journal.pone.0147470. eCollection 2016.
Alzheimer´s disease is the most prominent type of dementia and currently no causative treatment is available. According to recent studies, oligomeric species of the amyloid beta (Aβ) peptide appear to be the most toxic Aβ assemblies. Aβ monomers, however, may be not toxic per se and may even have a neuroprotective role. Here we describe a competitive mirror image phage display procedure that allowed us to identify preferentially Aβ1-42 monomer binding and thereby stabilizing peptides, which destabilize and thereby eliminate toxic oligomer species. One of the peptides, called Mosd1 (monomer specific d-peptide 1), was characterized in more detail. Mosd1 abolished oligomers from a mixture of Aβ1-42 species, reduced Aβ1-42 toxicity in cell culture, and restored the physiological phenotype in neuronal cells stably transfected with the gene coding for human amyloid precursor protein.
阿尔茨海默病是最常见的痴呆类型,目前尚无有效的病因治疗方法。根据最近的研究,淀粉样β(Aβ)肽的寡聚体似乎是毒性最强的Aβ聚集体。然而,Aβ单体本身可能无毒,甚至可能具有神经保护作用。在这里,我们描述了一种竞争性镜像噬菌体展示方法,该方法使我们能够优先识别Aβ1-42单体结合并稳定肽,这些肽会破坏有毒寡聚体的稳定性并将其消除。其中一种肽,称为Mosd1(单体特异性d肽1),得到了更详细的表征。Mosd1消除了Aβ1-42物种混合物中的寡聚体,降低了细胞培养中Aβ1-42的毒性,并恢复了稳定转染了编码人淀粉样前体蛋白基因的神经元细胞的生理表型。