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α-Synuclein-induced deformation of small unilamellar vesicles.
Makasewicz, Katarzyna; Wennmalm, Stefan; Linse, Sara; Sparr, Emma.
Afiliación
  • Makasewicz K; Department of Physical Chemistry, Lund University, 221 00 Lund, Sweden.
  • Wennmalm S; Department of Applied Physics, SciLifeLab, Royal Institute of Technology, 171 65 Solna, Sweden.
  • Linse S; Department of Biochemistry and Structural Biology, Lund University, 221 00 Lund, Sweden.
  • Sparr E; Department of Physical Chemistry, Lund University, 221 00 Lund, Sweden.
QRB Discov ; 3: e10, 2022.
Article en En | MEDLINE | ID: mdl-37529290
α-Synuclein is a small neuronal protein that reversibly associates with lipid membranes. The membrane interactions are believed to be central to the healthy function of this protein involved in synaptic plasticity and neurotransmitter release. α-Synuclein has been speculated to induce vesicle fusion as well as fission, processes which are analogous to each other but proceed in different directions and involve different driving forces. In the current work, we analyse α-synuclein-induced small unilamellar vesicle deformation from a thermodynamics point of view. We show that the structures interpreted in the literature as fusion intermediates are in fact a stable deformed state and neither fusion nor vesicle clustering occurs. We speculate on the driving force for the observed deformation and put forward a hypothesis that α-synuclein self-assembly on the lipid membrane precedes and induces membrane remodelling.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: QRB Discov Año: 2022 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: QRB Discov Año: 2022 Tipo del documento: Article País de afiliación: Suecia