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Inhibition of Aβ 16-22 Aggregation by [TEA] + [Ms] - Follows Weakening of the Hydrophobic Core and Sequestration of Peptides in Ionic Liquid Nanodomains
We developed a coarse-grained model for the protic ionic liquid, triethylammonium mesylate ([TEA] [Ms] ), to characterize its inhibitory effects on amyloid aggregation using the K LVFFAE fragment of the amyloid-β (Aβ ) as a model amyloidogenic peptide. In agreement with previous experiments, coarse-...
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Published in: | The journal of physical chemistry. B 2024-09, Vol.128 (38), p.9143-9150 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | We developed a coarse-grained model for the protic ionic liquid, triethylammonium mesylate ([TEA]
[Ms]
), to characterize its inhibitory effects on amyloid aggregation using the K
LVFFAE
fragment of the amyloid-β (Aβ
) as a model amyloidogenic peptide. In agreement with previous experiments, coarse-grained molecular dynamics simulations showed that increasing concentrations of [TEA]
[Ms]
in aqueous media led to increasingly small Aβ
aggregates with low beta-sheet contents. The cause of [TEA]
[Ms]
's inhibition of peptide aggregation was found to be a result of two interrelated effects. At a local scale, the enrichment of interactions between [TEA]
cations and hydrophobic phenylalanine side chains weakened the hydrophobic cores of amyloid aggregates, resulting in poorly ordered structures. At a global level, peptides tended to localize at the interfaces of IL-rich nanostructures with water. At high IL concentrations, when the IL-water interface was large or fragmented, Aβ
peptides were dispersed in the simulation cell, sometimes sequestered at unaggregated monomeric states. Together, these phenomena underlie [TEA]
[Ms]
's inhibition of amyloid aggregation. This work addresses the critical lack of knowledge on the mechanisms of protein-ionic liquid interactions and may have broader implications for industrial applications. |
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ISSN: | 1520-6106 1520-5207 |
DOI: | 10.1021/acs.jpcb.4c05135 |