Morphology-Dependent Interactions between α-Synuclein Monomers and Fibrils

Tinna Pálmadóttir*, Christopher A. Waudby, Katja Bernfur, John Christodoulou, Sara Linse*, Anders Malmendal

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Amyloid fibrils may adopt different morphologies depending on the solution conditions and the protein sequence. Here, we show that two chemically identical but morphologically distinct α-synuclein fibrils can form under identical conditions. This was observed by nuclear magnetic resonance (NMR), circular dichroism (CD), and fluorescence spectroscopy, as well as by cryo-transmission electron microscopy (cryo-TEM). The results show different surface properties of the two morphologies, A and B. NMR measurements show that monomers interact differently with the different fibril surfaces. Only a small part of the N-terminus of the monomer interacts with the fibril surface of morphology A, compared to a larger part of the monomer for morphology B. Differences in ThT binding seen by fluorescence titrations, and mesoscopic structures seen by cryo-TEM, support the conclusion of the two morphologies having different surface properties. Fibrils of morphology B were found to have lower solubility than A. This indicates that fibrils of morphology B are thermodynamically more stable, implying a chemical potential of fibrils of morphology B that is lower than that of morphology A. Consequently, at prolonged incubation time, fibrils of morphology B remained B, while an initially monomorphic sample of morphology A gradually transformed to B.

Original languageEnglish
Article number5191
JournalInternational Journal of Molecular Sciences
Volume24
Issue number6
ISSN1661-6596
DOIs
Publication statusPublished - Mar 2023

Bibliographical note

Funding Information:
This research was funded by the Swedish Research Council, grants number 2015-00143 (S.L.) and 2019-02397 (S.L.), the Novonordisk Foundation, grant number NNF18OC0054635 (S.L.), a Well-come Trust Investigator Award, grant number 206409/Z/17/Z (J.C.)

Keywords

  • aggregation
  • monomorphic
  • morphology
  • NMR spectroscopy
  • polymorphic
  • self-assembly
  • stability

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