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Towards a Pharmacophore for Amyloid

Diagnosing and treating Alzheimer's and other diseases associated with amyloid fibers remains a great challenge despite intensive research. To aid in this effort, we present atomic structures of fiber-forming segments of proteins involved in Alzheimer's disease in complex with small molecu...

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Detalles Bibliográficos
Autores principales: Landau, Meytal, Sawaya, Michael R., Faull, Kym F., Laganowsky, Arthur, Jiang, Lin, Sievers, Stuart A., Liu, Jie, Barrio, Jorge R., Eisenberg, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114762/
https://www.ncbi.nlm.nih.gov/pubmed/21695112
http://dx.doi.org/10.1371/journal.pbio.1001080
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author Landau, Meytal
Sawaya, Michael R.
Faull, Kym F.
Laganowsky, Arthur
Jiang, Lin
Sievers, Stuart A.
Liu, Jie
Barrio, Jorge R.
Eisenberg, David
author_facet Landau, Meytal
Sawaya, Michael R.
Faull, Kym F.
Laganowsky, Arthur
Jiang, Lin
Sievers, Stuart A.
Liu, Jie
Barrio, Jorge R.
Eisenberg, David
author_sort Landau, Meytal
collection PubMed
description Diagnosing and treating Alzheimer's and other diseases associated with amyloid fibers remains a great challenge despite intensive research. To aid in this effort, we present atomic structures of fiber-forming segments of proteins involved in Alzheimer's disease in complex with small molecule binders, determined by X-ray microcrystallography. The fiber-like complexes consist of pairs of β-sheets, with small molecules binding between the sheets, roughly parallel to the fiber axis. The structures suggest that apolar molecules drift along the fiber, consistent with the observation of nonspecific binding to a variety of amyloid proteins. In contrast, negatively charged orange-G binds specifically to lysine side chains of adjacent sheets. These structures provide molecular frameworks for the design of diagnostics and drugs for protein aggregation diseases.
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spelling pubmed-31147622011-06-21 Towards a Pharmacophore for Amyloid Landau, Meytal Sawaya, Michael R. Faull, Kym F. Laganowsky, Arthur Jiang, Lin Sievers, Stuart A. Liu, Jie Barrio, Jorge R. Eisenberg, David PLoS Biol Research Article Diagnosing and treating Alzheimer's and other diseases associated with amyloid fibers remains a great challenge despite intensive research. To aid in this effort, we present atomic structures of fiber-forming segments of proteins involved in Alzheimer's disease in complex with small molecule binders, determined by X-ray microcrystallography. The fiber-like complexes consist of pairs of β-sheets, with small molecules binding between the sheets, roughly parallel to the fiber axis. The structures suggest that apolar molecules drift along the fiber, consistent with the observation of nonspecific binding to a variety of amyloid proteins. In contrast, negatively charged orange-G binds specifically to lysine side chains of adjacent sheets. These structures provide molecular frameworks for the design of diagnostics and drugs for protein aggregation diseases. Public Library of Science 2011-06-14 /pmc/articles/PMC3114762/ /pubmed/21695112 http://dx.doi.org/10.1371/journal.pbio.1001080 Text en Landau 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Landau, Meytal
Sawaya, Michael R.
Faull, Kym F.
Laganowsky, Arthur
Jiang, Lin
Sievers, Stuart A.
Liu, Jie
Barrio, Jorge R.
Eisenberg, David
Towards a Pharmacophore for Amyloid
title Towards a Pharmacophore for Amyloid
title_full Towards a Pharmacophore for Amyloid
title_fullStr Towards a Pharmacophore for Amyloid
title_full_unstemmed Towards a Pharmacophore for Amyloid
title_short Towards a Pharmacophore for Amyloid
title_sort towards a pharmacophore for amyloid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114762/
https://www.ncbi.nlm.nih.gov/pubmed/21695112
http://dx.doi.org/10.1371/journal.pbio.1001080
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