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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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 |
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author | Rudolph, Stephan Klein, Antonia Nicole Tusche, Markus Schlosser, Christine Elfgen, Anne Brener, Oleksandr Teunissen, Charlotte Gremer, Lothar Funke, Susanne Aileen Kutzsche, Janine Willbold, Dieter |
author_facet | Rudolph, Stephan Klein, Antonia Nicole Tusche, Markus Schlosser, Christine Elfgen, Anne Brener, Oleksandr Teunissen, Charlotte Gremer, Lothar Funke, Susanne Aileen Kutzsche, Janine Willbold, Dieter |
author_sort | Rudolph, Stephan |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4740492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47404922016-02-11 Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity Rudolph, Stephan Klein, Antonia Nicole Tusche, Markus Schlosser, Christine Elfgen, Anne Brener, Oleksandr Teunissen, Charlotte Gremer, Lothar Funke, Susanne Aileen Kutzsche, Janine Willbold, Dieter PLoS One Research Article 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. Public Library of Science 2016-02-03 /pmc/articles/PMC4740492/ /pubmed/26840229 http://dx.doi.org/10.1371/journal.pone.0147470 Text en © 2016 Rudolph et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Rudolph, Stephan Klein, Antonia Nicole Tusche, Markus Schlosser, Christine Elfgen, Anne Brener, Oleksandr Teunissen, Charlotte Gremer, Lothar Funke, Susanne Aileen Kutzsche, Janine Willbold, Dieter Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity |
title | Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity |
title_full | Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity |
title_fullStr | Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity |
title_full_unstemmed | Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity |
title_short | Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and Toxicity |
title_sort | competitive mirror image phage display derived peptide modulates amyloid beta aggregation and toxicity |
topic | Research Article |
url | 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 |
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