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
- 192Citations
- 266Captures
- 21Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations192
- Citation Indexes189
- 189
- CrossRef158
- Policy Citations2
- Policy Citation2
- Patent Family Citations1
- Patent Families1
- Captures266
- Readers266
- 266
- Mentions21
- News Mentions16
- News16
- Blog Mentions5
- Blog5
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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
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85046548678&origin=inward; http://dx.doi.org/10.1038/s41557-018-0031-x; http://www.ncbi.nlm.nih.gov/pubmed/29736006; https://www.nature.com/articles/s41557-018-0031-x; https://dx.doi.org/10.1038/s41557-018-0031-x; https://f1000.com/prime/733174692#eval793552220
Springer Science and Business Media LLC
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