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Cholesterol catalyses Aβ42 aggregation through a heterogeneous nucleation pathway in the presence of lipid membranes

Nature Chemistry, ISSN: 1755-4349, Vol: 10, Issue: 6, Page: 673-683
2018
  • 192
    Citations
  • 0
    Usage
  • 266
    Captures
  • 21
    Mentions
  • 70
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    192
    • Citation Indexes
      189
    • Policy Citations
      2
      • Policy Citation
        2
    • Patent Family Citations
      1
      • Patent Families
        1
  • Captures
    266
  • Mentions
    21
    • News Mentions
      16
      • News
        16
    • Blog Mentions
      5
      • Blog
        5
  • Social Media
    70
    • Shares, Likes & Comments
      70
      • Facebook
        70

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Article Description

Alzheimer's disease is a neurodegenerative disorder associated with the aberrant aggregation of the amyloid-β peptide. Although increasing evidence implicates cholesterol in the pathogenesis of Alzheimer's disease, the detailed mechanistic link between this lipid molecule and the disease process remains to be fully established. To address this problem, we adopt a kinetics-based strategy that reveals a specific catalytic role of cholesterol in the aggregation of Aβ42 (the 42-residue form of the amyloid-β peptide). More specifically, we demonstrate that lipid membranes containing cholesterol promote Aβ42 aggregation by enhancing its primary nucleation rate by up to 20-fold through a heterogeneous nucleation pathway. We further show that this process occurs as a result of cooperativity in the interaction of multiple cholesterol molecules with Aβ42. These results identify a specific microscopic pathway by which cholesterol dramatically enhances the onset of Aβ42 aggregation, thereby helping rationalize the link between Alzheimer's disease and the impairment of cholesterol homeostasis.

Bibliographic Details

Habchi, Johnny; Chia, Sean; Galvagnion, Céline; Michaels, Thomas C. T.; Bellaiche, Mathias M. J.; Ruggeri, Francesco Simone; Sanguanini, Michele; Idini, Ilaria; Kumita, Janet R.; Sparr, Emma; Linse, Sara; Dobson, Christopher M.; Knowles, Tuomas P. J.; Vendruscolo, Michele

Springer Science and Business Media LLC

Chemistry; Chemical Engineering

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