bioRxivBiophysics
Transient interactions between the fuzzy coat and the cross-β core of brain-derived Aβ42 filaments
Abstract
A wide range of human disorders, including Alzheimers disease (AD), are characterised by the aberrant formation of amyloid fibrils. Amyloid fibrils are filamentous structures characterized by the presence of a highly-ordered cross-{beta} core. In many cases, this core structure is flanked by disordered regions, often referred to as fuzzy coat. The structural properties of fuzzy coats, and the way in which they interact with their environments, however, have not been described in full detail to date. Here, we generated the conformational ensembles of two brain-derived amyloid filaments of A{beta}42, corresponding respectively to familial and sporadic forms of AD. The approach that we used, called metadynamic electron microscopy metainference (MEMMI), enabled us to provide a characterization of the transient interactions between the fuzzy coat and the cross-{beta} core of the filaments. These calculations indicated that the familial AD filaments are less soluble than the sporadic AD filaments, and that the fuzzy coat contributes to increasing the solubility of both types of filament. In addition, by analyzing the deviations between the density maps from cryo-EM and from the MEMMI structural ensembles, we observed a slowing down in the diffusion of water and sodium ions near the surface of the filaments, offering insight into the hydration dynamics of amyloid fibrils. These results illustrate how the metainference approach can help analyse cryo-EM maps for the characterisation of the properties of amyloid fibrils.
- organism: human
- assay: cryo-EM
- assay: electronic health records
- research focus: protein folding & dynamics
- research focus: cell type annotation
- approach: deep learning
- approach: statistical model
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
- Aβ Fibrils Can Act as Aqueous Pores: a Molecular Dynamics Study
Sashin Natesh, Joseph R. Sachleben, … Esmael J. Haddadian·bioRxiv·Sep 14, 2018
- Cryo-EM structures of lipidic fibrils of amyloid-β (1-40)
Benedikt Frieg, Mookyoung Han, … G.F. Schroeder·Nature CommunicationsPeer-reviewed·Feb 13, 2024
- Determination of the structure and dynamics of the fuzzy coat of an amyloid fibril of IAPP using cryo-electron microscopy
Z. F. Brotzakis, T. Löhr, … M. Vendruscolo·bioRxiv·May 29, 2022
- Atomic structures of medin and Aβ fibrils reveal polymorphic remodeling in mixed amyloid systems
Brajabandhu Pradhan, Senthil T. Kumar, … Joost W. H. Schymkowitz·bioRxiv·Jul 17, 2025
- Cryo-EM structures of Aβ40 filaments from the leptomeninges of individuals with Alzheimer's disease and cerebral amyloid angiopathy
Yang Yang, Alexey G. Murzin, … Sjors H. W. Scheres·Acta Neuropathologica CommunicationsPeer-reviewed·Dec 4, 2023
- Distinct Filament Conformation for Receptor-Bound Amyloid-β from Alzheimers Disease Brain
Mikhail A. Kostylev, Carmen Butan, … Stephen M. Strittmatter·Nature CommunicationsPeer-reviewed·Jul 22, 2026