Nanoscale AdvancesBiophysicsPeer-reviewed journal article
Dynamic instability in nanoscale lipid domains revealed by contact mode high speed AFM: effect of amyloid-β and cholesterol content
Morgan J. RobinsoniD, Loren PiccoiD, Oliver PaytoniD, Nikolas Zelem, Charlotte Baur, Michael A. BeazelyiD, Mervyn John MilesiD, Zoya LeonenkoiD
Abstract
Cellular membranes are an essential feature of life, the composition and structure of which is important in governing cellular processes and is linked to multiple disorders. Of particular interest is the role that the lipid membrane plays in amyloidogenic diseases such as Alzheimers disease (AD), including the role of lipid composition and cholesterol in mediating amyloid toxicity. To mimic neuronal membranes, we used 3-component (DPPC/DOPC/Chol) and 5-component (DPPC/POPC/Chol/sphingomyelin/GM1) model membranes. Atomic force microscopy (AFM) is a key tool in studying the structures of lipid membranes and their interactions with amyloid. Recent advances in contact mode high-speed AFM (HS-AFM) have made it possible to capture dynamic processes at video rate. We used a unique custom-built contact mode HS-AFM to image model lipid membranes and study amyloid-{beta} interactions in liquid. We demonstrate the advantage of using HS-AFM coupled with spatiotemporal variability analysis to capture the dynamic interaction of A{beta} 1-42 monomers and oligomers with phase separated lipid bilayers to elucidate the role of nanoscale domains in amyloid-membrane interactions. We show that amyloid oligomer complexes induce greater dynamic instability than monomers, and that low cholesterol membranes are more susceptible to destabilization. Overall, we demonstrate the advantage of HS-AFM to image biological processes on biologically relevant soft samples and discuss tip-sample interactions at high-speed operation in contact mode on lipid membrane models in liquid environment. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=62 SRC="FIGDIR/small/633021v2_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@8a7da2org.highwire.dtl.DTLVardef@3e39d5org.highwire.dtl.DTLVardef@1470050org.highwire.dtl.DTLVardef@658f19_HPS_FORMAT_FIGEXP M_FIG C_FIG
- assay: imaging
- research focus: cell signaling & trafficking
- research focus: host-pathogen & immune response
- research focus: protein folding & dynamics
- approach: microscopy & imaging analysis
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 16th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Cholesterol in membranes facilitates aggregation of amyloid beta protein at physiologically low concentrations
S. Banerjee, M. Hashemi, … Y. L. Lyubchenko·bioRxiv·Sep 6, 2020
- A Coarse-Grained Molecular Dynamics Investigation on Spontaneous Binding of Aβ1-40 Fibrils with Cholesterol-mixed DPPC Bilayers
N. Agrawal, A. A. Skelton, E. Parisini·bioRxiv·Sep 16, 2022
- Effects of Cholesterol on Amyloid-induced Membrane Poration
Yanxing Yang, Bibhuti Shah, … Andrew J. Nieuwkoop·bioRxiv·Aug 15, 2025
- 3D-Visualization of Amyloid-β Oligomer and Fibril Interactions with Lipid Membranes by Cryo-Electron Tomography
Y. Tian, R. Liang, … J. H. Viles·Chemical SciencePeer-reviewed·Jan 1, 2021
- Amyloid β interaction with membranes: Removal of cholesterol from the membranes to catalyze aggregation and amyloid pathology
Rishiram Baral, Ruan van Deventer, Yuri L. Lyubchenko·bioRxiv·Aug 20, 2025
- Distinct Aβ40 and Aβ42 co-assembly pathways with free lipids: Experiment-driven MD study
Rachit Pandey, Tarek Olabi, … Brigita Urbanc·bioRxiv·Oct 2, 2026