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J Phys Chem B ; 128(23): 5667-5675, 2024 Jun 13.
Article in English | MEDLINE | ID: mdl-38836448

ABSTRACT

Nonspecific membrane disruption is considered a plausible mechanism for the cytotoxicity induced by ß-amyloid (Aß) aggregates. In scenarios of high local Aß concentrations, a two-step membrane fragmentation model has been proposed. Initially, membrane-embedded Aß oligomeric aggregates form, followed by membrane fragmentation. However, the key molecular-level interactions between Aß oligomeric aggregates and lipids that drive the second-stage membrane fragmentation remain unclear. This study monitors the time-dependent changes in lipid dynamics and water accessibility of model liposomes during Aß-induced membrane fragmentation. Our results indicate that lipid dynamics on the nanosecond to microsecond time scale undergo rapid acceleration upon initial incubation with membrane-incorporated Aß oligomeric aggregates, followed by a slow deceleration process. Concurrently, lipid headgroups become less accessible to water. Both observations suggest a carpet-like mechanism of membrane disruption for the Aß-induced membrane fragmentation process.


Subject(s)
Amyloid beta-Peptides , Amyloid beta-Peptides/chemistry , Amyloid beta-Peptides/metabolism , Liposomes/chemistry , Liposomes/metabolism , Protein Aggregates/drug effects , Water/chemistry , Cell Membrane/metabolism , Cell Membrane/chemistry
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