Distinct Mechanisms Determine α-Synuclein Fibril Morphology during Growth and Maturation

A. Sidhu, Gezina M.J. Segers-Nolten, V. Raussens, Mireille Maria Anna Elisabeth Claessens, Vinod Subramaniam

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Abstract

Amyloid polymorphs have become one of the focal points of molecular studies of neurodegenerative diseases like Parkinson’s disease. Due to their distinct biochemical properties and prion-like characteristics, insights into the molecular origin and stability of amyloid polymorphs over time are crucial for understanding the potential role of amyloid polymorphism in these diseases. Here, we systematically study the fibrillization of recombinantly produced human α-synuclein (αSyn) over an extended period of time to unravel the origin and temporal evolution of polymorphism. We follow morphological changes in the same fibril sample with atomic force microscopy over a period of 1 year. We show that wild-type (wt) αSyn fibrils undergo a slow maturation over time after reaching the plateau phase of aggregation (as detected in a Thioflavin-T fluorescence assay). This maturation, visualized by changes in the fibril periodicity over time, is absent in the disease mutant fibrils. The β-sheet content of the plateau phase and matured fibrils, obtained using Fourier transform infrared spectroscopy, is however similar for the αSyn protein sequences, suggesting that the morphological changes in wt αSyn fibrils are tertiary or quaternary in origin. Furthermore, results from a reversibility assay show that the plateau phase fibrils do not disassemble over time. Together, the observed changes in the periodicity distributions and stability of the fibrillar core over time point toward two distinct mechanisms that determine the morphology of wt αSyn fibrils: competitive growth between different polymorphs during the fibrillization phase followed by a process wherein fibrils undergo slow maturation or annealing.
Original languageEnglish
Pages (from-to)538-547
JournalACS chemical neuroscience
Volume8
Issue number3
DOIs
Publication statusPublished - 15 Mar 2017

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Synucleins
Polymorphism
Amyloid
Growth
Assays
Periodicity
Neurodegenerative diseases
Prions
Atomic force microscopy
Atomic Force Microscopy
Agglomeration
Fourier Transform Infrared Spectroscopy
Fluorescence
Annealing
Neurodegenerative Diseases
Parkinson Disease
Proteins

Keywords

  • METIS-318781
  • IR-103814

Cite this

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abstract = "Amyloid polymorphs have become one of the focal points of molecular studies of neurodegenerative diseases like Parkinson’s disease. Due to their distinct biochemical properties and prion-like characteristics, insights into the molecular origin and stability of amyloid polymorphs over time are crucial for understanding the potential role of amyloid polymorphism in these diseases. Here, we systematically study the fibrillization of recombinantly produced human α-synuclein (αSyn) over an extended period of time to unravel the origin and temporal evolution of polymorphism. We follow morphological changes in the same fibril sample with atomic force microscopy over a period of 1 year. We show that wild-type (wt) αSyn fibrils undergo a slow maturation over time after reaching the plateau phase of aggregation (as detected in a Thioflavin-T fluorescence assay). This maturation, visualized by changes in the fibril periodicity over time, is absent in the disease mutant fibrils. The β-sheet content of the plateau phase and matured fibrils, obtained using Fourier transform infrared spectroscopy, is however similar for the αSyn protein sequences, suggesting that the morphological changes in wt αSyn fibrils are tertiary or quaternary in origin. Furthermore, results from a reversibility assay show that the plateau phase fibrils do not disassemble over time. Together, the observed changes in the periodicity distributions and stability of the fibrillar core over time point toward two distinct mechanisms that determine the morphology of wt αSyn fibrils: competitive growth between different polymorphs during the fibrillization phase followed by a process wherein fibrils undergo slow maturation or annealing.",
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Distinct Mechanisms Determine α-Synuclein Fibril Morphology during Growth and Maturation. / Sidhu, A.; Segers-Nolten, Gezina M.J.; Raussens, V.; Claessens, Mireille Maria Anna Elisabeth; Subramaniam, Vinod.

In: ACS chemical neuroscience, Vol. 8, No. 3, 15.03.2017, p. 538-547.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Distinct Mechanisms Determine α-Synuclein Fibril Morphology during Growth and Maturation

AU - Sidhu, A.

AU - Segers-Nolten, Gezina M.J.

AU - Raussens, V.

AU - Claessens, Mireille Maria Anna Elisabeth

AU - Subramaniam, Vinod

PY - 2017/3/15

Y1 - 2017/3/15

N2 - Amyloid polymorphs have become one of the focal points of molecular studies of neurodegenerative diseases like Parkinson’s disease. Due to their distinct biochemical properties and prion-like characteristics, insights into the molecular origin and stability of amyloid polymorphs over time are crucial for understanding the potential role of amyloid polymorphism in these diseases. Here, we systematically study the fibrillization of recombinantly produced human α-synuclein (αSyn) over an extended period of time to unravel the origin and temporal evolution of polymorphism. We follow morphological changes in the same fibril sample with atomic force microscopy over a period of 1 year. We show that wild-type (wt) αSyn fibrils undergo a slow maturation over time after reaching the plateau phase of aggregation (as detected in a Thioflavin-T fluorescence assay). This maturation, visualized by changes in the fibril periodicity over time, is absent in the disease mutant fibrils. The β-sheet content of the plateau phase and matured fibrils, obtained using Fourier transform infrared spectroscopy, is however similar for the αSyn protein sequences, suggesting that the morphological changes in wt αSyn fibrils are tertiary or quaternary in origin. Furthermore, results from a reversibility assay show that the plateau phase fibrils do not disassemble over time. Together, the observed changes in the periodicity distributions and stability of the fibrillar core over time point toward two distinct mechanisms that determine the morphology of wt αSyn fibrils: competitive growth between different polymorphs during the fibrillization phase followed by a process wherein fibrils undergo slow maturation or annealing.

AB - Amyloid polymorphs have become one of the focal points of molecular studies of neurodegenerative diseases like Parkinson’s disease. Due to their distinct biochemical properties and prion-like characteristics, insights into the molecular origin and stability of amyloid polymorphs over time are crucial for understanding the potential role of amyloid polymorphism in these diseases. Here, we systematically study the fibrillization of recombinantly produced human α-synuclein (αSyn) over an extended period of time to unravel the origin and temporal evolution of polymorphism. We follow morphological changes in the same fibril sample with atomic force microscopy over a period of 1 year. We show that wild-type (wt) αSyn fibrils undergo a slow maturation over time after reaching the plateau phase of aggregation (as detected in a Thioflavin-T fluorescence assay). This maturation, visualized by changes in the fibril periodicity over time, is absent in the disease mutant fibrils. The β-sheet content of the plateau phase and matured fibrils, obtained using Fourier transform infrared spectroscopy, is however similar for the αSyn protein sequences, suggesting that the morphological changes in wt αSyn fibrils are tertiary or quaternary in origin. Furthermore, results from a reversibility assay show that the plateau phase fibrils do not disassemble over time. Together, the observed changes in the periodicity distributions and stability of the fibrillar core over time point toward two distinct mechanisms that determine the morphology of wt αSyn fibrils: competitive growth between different polymorphs during the fibrillization phase followed by a process wherein fibrils undergo slow maturation or annealing.

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KW - IR-103814

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SP - 538

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JO - ACS chemical neuroscience

JF - ACS chemical neuroscience

SN - 1948-7193

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