alpha-synuclein: amyloid fibrils and interactions with lipid membranes
(2021)- Abstract
- The second most common neurodegenerative disease, Parkinson’s disease, is linked with an amyloid forming protein, alpha-synuclein. Hallmarks of Parkinson’s disease are progressive loss of dopaminergic neurons and accumulation of intraneuronal inclusions termed Lewy bodies. Major components of Lewy bodies are amyloid fibrils formed by alpha-synuclein and various lipids and cell organelles.
In this thesis, we investigated the interaction of alpha-synuclein and different model lipid membranes. The main techniques have been small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS). We focused on the structure of alpha-synuclein fibrils and model lipid membranes, both alone and when in the presence of each other.... (More) - The second most common neurodegenerative disease, Parkinson’s disease, is linked with an amyloid forming protein, alpha-synuclein. Hallmarks of Parkinson’s disease are progressive loss of dopaminergic neurons and accumulation of intraneuronal inclusions termed Lewy bodies. Major components of Lewy bodies are amyloid fibrils formed by alpha-synuclein and various lipids and cell organelles.
In this thesis, we investigated the interaction of alpha-synuclein and different model lipid membranes. The main techniques have been small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS). We focused on the structure of alpha-synuclein fibrils and model lipid membranes, both alone and when in the presence of each other. The investigations were performed when the protein was present both in its monomeric and fibrillar form. We also studied fibril formation process in the presence of model membranes and followed the effect it has on the membrane structure, as well as the effect membranes have on the structure of mature fibrils. Finally, we investigated arrangement of colloidally unstable alpha-synuclein fibrils and their interaction with various lipid membranes.
We learned that interaction of monomeric alpha-synuclein and lipid disc micelles results in a major deformation of the disc shape, but that the partial recovery is possible due to the desorption of monomers and their incorporation into amyloid fibrils. We also learned that the fibril formation can cause vesicle fusion. The presence of model membranes during the fibril formation has no effect on the cross-sectional size and structure of fibrils, nor is there any observable incorporation of lipid molecules into the mature fibrils. The colloidally unstable alpha-synuclein fibrils arrange into mass clusters, independent on the presence of different lipid vesicles, and this arrangement is reproduced with a simple rigid-rod cluster model. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/32bea91d-187c-4742-8d7c-3ccf042fd03c
- author
- Dubackic, Marija LU
- supervisor
-
- Sara Snogerup-Linse LU
- Ulf Olsson LU
- Emma Sparr LU
- opponent
-
- Professor Mezzenga, Raffaele, ETH Zürich
- organization
- publishing date
- 2021
- type
- Thesis
- publication status
- published
- subject
- keywords
- alpha-synuclein, model lipid membranes, amyloid fibrils, Parkinson's disease, Lewy bodies, SANS, SAXS
- pages
- 198 pages
- publisher
- Lund University
- defense location
- Kemicentrum KC:A, Lund. Join via Zoom: https://lu-se.zoom.us/j/64263865014/ or Live-streaming channel: https://www.youtube.com/channel/UCnuD6zyuQ4vwg9zSBeTQoQQ/featured
- defense date
- 2021-12-16 13:00:00
- ISBN
- 978-91-7422-840-3
- 978-91-7422-841-0
- language
- English
- LU publication?
- yes
- id
- 32bea91d-187c-4742-8d7c-3ccf042fd03c
- date added to LUP
- 2021-11-18 10:46:58
- date last changed
- 2025-04-04 14:56:22
@phdthesis{32bea91d-187c-4742-8d7c-3ccf042fd03c,
abstract = {{The second most common neurodegenerative disease, Parkinson’s disease, is linked with an amyloid forming protein, alpha-synuclein. Hallmarks of Parkinson’s disease are progressive loss of dopaminergic neurons and accumulation of intraneuronal inclusions termed Lewy bodies. Major components of Lewy bodies are amyloid fibrils formed by alpha-synuclein and various lipids and cell organelles. <br/><br/>In this thesis, we investigated the interaction of alpha-synuclein and different model lipid membranes. The main techniques have been small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS). We focused on the structure of alpha-synuclein fibrils and model lipid membranes, both alone and when in the presence of each other. The investigations were performed when the protein was present both in its monomeric and fibrillar form. We also studied fibril formation process in the presence of model membranes and followed the effect it has on the membrane structure, as well as the effect membranes have on the structure of mature fibrils. Finally, we investigated arrangement of colloidally unstable alpha-synuclein fibrils and their interaction with various lipid membranes.<br/><br/>We learned that interaction of monomeric alpha-synuclein and lipid disc micelles results in a major deformation of the disc shape, but that the partial recovery is possible due to the desorption of monomers and their incorporation into amyloid fibrils. We also learned that the fibril formation can cause vesicle fusion. The presence of model membranes during the fibril formation has no effect on the cross-sectional size and structure of fibrils, nor is there any observable incorporation of lipid molecules into the mature fibrils. The colloidally unstable alpha-synuclein fibrils arrange into mass clusters, independent on the presence of different lipid vesicles, and this arrangement is reproduced with a simple rigid-rod cluster model.}},
author = {{Dubackic, Marija}},
isbn = {{978-91-7422-840-3}},
keywords = {{alpha-synuclein; model lipid membranes; amyloid fibrils; Parkinson's disease; Lewy bodies; SANS; SAXS}},
language = {{eng}},
publisher = {{Lund University}},
school = {{Lund University}},
title = {{alpha-synuclein: amyloid fibrils and interactions with lipid membranes}},
url = {{https://lup.lub.lu.se/search/files/109871602/Marija_Dubackic_web.pdf}},
year = {{2021}},
}