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Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity

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...

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Detalles Bibliográficos
Autores principales: Rudolph, Stephan, Klein, Antonia Nicole, Tusche, Markus, Schlosser, Christine, Elfgen, Anne, Brener, Oleksandr, Teunissen, Charlotte, Gremer, Lothar, Funke, Susanne Aileen, Kutzsche, Janine, Willbold, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740492/
https://www.ncbi.nlm.nih.gov/pubmed/26840229
http://dx.doi.org/10.1371/journal.pone.0147470
Descripción
Sumario: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 Aβ(1–42) 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 Aβ(1–42) species, reduced Aβ(1–42) toxicity in cell culture, and restored the physiological phenotype in neuronal cells stably transfected with the gene coding for human amyloid precursor protein.