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Cholesterol facilitates interactions between α‐synuclein oligomers and charge‐neutral membranes
- Source :
- FEBS Letters. 589:2661-2667
- Publication Year :
- 2015
- Publisher :
- Wiley, 2015.
-
Abstract
- Oligomeric species formed during α-synuclein fibrillation are suggested to be membrane-disrupting agents, and have been associated with cytotoxicity in Parkinson’s disease. The majority of studies, however, have revealed that the effect of α-synuclein oligomers is only noticeable on systems composed of anionic lipids, while the more physiologically relevant zwitterionic lipids remain intact. We present experimental evidence for significant morphological changes in zwitterionic membranes containing cholesterol, induced by α-synuclein oligomers. Depending on the lipid composition, model membranes are either unperturbed, disrupt, or undergo dramatic morphological changes and segregate into structurally different components, which we visualize by 2-photon fluorescence microscopy and generalized polarization analysis using the fluorescent probe Laurdan. Our results highlight the crucial role of cholesterol for mediating interactions between physiologically relevant membranes and α-synuclein.
- Subjects :
- Amyloid
Parkinson's disease
Fluorescent Dye
Biophysics
Plasma protein binding
Biochemistry
Oligomer
Protein Structure, Secondary
Multiphoton microscopy
Membrane phase separation
Cell membrane
chemistry.chemical_compound
Genetic
Structural Biology
2-Naphthylamine
Laurdan fluorescence
Genetics
Fluorescence microscope
medicine
Molecular Biology
Fluorescent Dyes
Laurate
α-Synuclein
Membranes
Chemistry
Medicine (all)
Cell Membrane
Membrane
Cell Biology
Settore FIS/07 - Fisica Applicata(Beni Culturali, Ambientali, Biol.e Medicin)
Cholesterol
medicine.anatomical_structure
Biophysic
Structural biology
alpha-Synuclein
Parkinson’s disease
Protein Multimerization
Laurdan
Laurates
Protein Binding
Subjects
Details
- ISSN :
- 18733468 and 00145793
- Volume :
- 589
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....69279e193ce747166c8ae46ac9109a3d
- Full Text :
- https://doi.org/10.1016/j.febslet.2015.08.013