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Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein

BACKGROUND: Lewy body in the substantia nigra is a cardinal pathological feature of Parkinson's disease. Despite enormous efforts, the cause-and-effect relationship between Lewy body formation and the disorder is yet to be explicitly unveiled. METHODOLOGY/PRINCIPAL FINDINGS: Here, we showed tha...

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Autores principales: Lee, Jung-Ho, Hong, Chul-Suk, Lee, Soonkoo, Yang, Jee-Eun, Park, Yong Il, Lee, Daekyun, Hyeon, Taeghwan, Jung, Seunho, Paik, Seung R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3471876/
https://www.ncbi.nlm.nih.gov/pubmed/23077644
http://dx.doi.org/10.1371/journal.pone.0047580
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author Lee, Jung-Ho
Hong, Chul-Suk
Lee, Soonkoo
Yang, Jee-Eun
Park, Yong Il
Lee, Daekyun
Hyeon, Taeghwan
Jung, Seunho
Paik, Seung R.
author_facet Lee, Jung-Ho
Hong, Chul-Suk
Lee, Soonkoo
Yang, Jee-Eun
Park, Yong Il
Lee, Daekyun
Hyeon, Taeghwan
Jung, Seunho
Paik, Seung R.
author_sort Lee, Jung-Ho
collection PubMed
description BACKGROUND: Lewy body in the substantia nigra is a cardinal pathological feature of Parkinson's disease. Despite enormous efforts, the cause-and-effect relationship between Lewy body formation and the disorder is yet to be explicitly unveiled. METHODOLOGY/PRINCIPAL FINDINGS: Here, we showed that radiating amyloid fibrils (RAFs) were instantly developed on the surface of synthetic lipid membranes from the β-sheet free oligomeric species of α-synuclein through a unit-assembly process. The burgeoning RAFs were successfully matured by feeding them with additional oligomers, which led to concomitant dramatic shrinkage and disintegration of the membranes by pulling off lipid molecules to the extending fibrils. Mitochondria and lysosomes were demonstrated to be disrupted by the oligomeric α-synuclein via membrane-dependent fibril formation. CONCLUSION: The physical structure formation of amyloid fibrils, therefore, could be considered as detrimental to the cells by affecting membrane integrity of the intracellular organelles, which might be a molecular cause for the neuronal degeneration observed in Parkinson's disease.
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spelling pubmed-34718762012-10-17 Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein Lee, Jung-Ho Hong, Chul-Suk Lee, Soonkoo Yang, Jee-Eun Park, Yong Il Lee, Daekyun Hyeon, Taeghwan Jung, Seunho Paik, Seung R. PLoS One Research Article BACKGROUND: Lewy body in the substantia nigra is a cardinal pathological feature of Parkinson's disease. Despite enormous efforts, the cause-and-effect relationship between Lewy body formation and the disorder is yet to be explicitly unveiled. METHODOLOGY/PRINCIPAL FINDINGS: Here, we showed that radiating amyloid fibrils (RAFs) were instantly developed on the surface of synthetic lipid membranes from the β-sheet free oligomeric species of α-synuclein through a unit-assembly process. The burgeoning RAFs were successfully matured by feeding them with additional oligomers, which led to concomitant dramatic shrinkage and disintegration of the membranes by pulling off lipid molecules to the extending fibrils. Mitochondria and lysosomes were demonstrated to be disrupted by the oligomeric α-synuclein via membrane-dependent fibril formation. CONCLUSION: The physical structure formation of amyloid fibrils, therefore, could be considered as detrimental to the cells by affecting membrane integrity of the intracellular organelles, which might be a molecular cause for the neuronal degeneration observed in Parkinson's disease. Public Library of Science 2012-10-15 /pmc/articles/PMC3471876/ /pubmed/23077644 http://dx.doi.org/10.1371/journal.pone.0047580 Text en © 2012 Lee 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
Lee, Jung-Ho
Hong, Chul-Suk
Lee, Soonkoo
Yang, Jee-Eun
Park, Yong Il
Lee, Daekyun
Hyeon, Taeghwan
Jung, Seunho
Paik, Seung R.
Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein
title Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein
title_full Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein
title_fullStr Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein
title_full_unstemmed Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein
title_short Radiating Amyloid Fibril Formation on the Surface of Lipid Membranes through Unit-Assembly of Oligomeric Species of α-Synuclein
title_sort radiating amyloid fibril formation on the surface of lipid membranes through unit-assembly of oligomeric species of α-synuclein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3471876/
https://www.ncbi.nlm.nih.gov/pubmed/23077644
http://dx.doi.org/10.1371/journal.pone.0047580
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