Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1782246487512580096 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3471876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT leejungho radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT hongchulsuk radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT leesoonkoo radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT yangjeeeun radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT parkyongil radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT leedaekyun radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT hyeontaeghwan radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT jungseunho radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein AT paikseungr radiatingamyloidfibrilformationonthesurfaceoflipidmembranesthroughunitassemblyofoligomericspeciesofasynuclein |