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research article

Understanding amyloid aggregation by statistical analysis of atomic force microscopy images

Adamcik, Jozef  
•
Jung, Jin-Mi
•
Flakowski, Jérôme
Show more
2010
Nature Nanotechnology

The aggregation of proteins is central to many aspects of daily life, including food processing, blood coagulation, eye cataract formation disease and prion-related neurodegenerative infections[1–5]. However, the physical mechanisms responsible for amyloidosis—the irreversible fibril formation of various proteins that is linked to disorders such as Alzheimer’s, Creutzfeldt–Jakob and Huntington’s diseases—have not yet been fully elucidated[6–9]. Here, we show that different stages of amyloid aggregation can be examined by performing a stat- istical polymer physics analysis of single-molecule atomic force microscopy images of heat-denatured b-lactoglobulin fibrils. The atomic force microscopy analysis, supported by theoretical arguments, reveals that the fibrils have a multistranded helical shape with twisted ribbon-like structures. Our results also indicate a possible general model for amyloid fibril assembly and illustrate the potential of this approach for investigating fibrillar systems. 1. Caughey, B. & Lansbury, P. T. Protofibrils, pores, fibrils and neurodegeneration: separating the responsible protein aggregates from the innocent bystanders. Annu. Rev. Neurosci. 26, 267–298 (2003). 2. Stradner, A. et al. Equilibrium cluster formation in concentrated protein solutions and colloids. Nature 432, 492–495 (2004). 3. Mezzenga, R., Schurtenberger, P., Burbidge, A. & Michel, M. Understanding foods as soft materials. Nature Mater. 4, 729–740 (2005). 4. Selkoe, D. J. Folding proteins in fatal ways. Nature 426, 900–904 (2003). 5. Chiti, F. & Dobson, C. M. Amyloid formation by globular proteins under native conditions. Nature Chem. Biol. 5, 15–22 (2009). 6. Knowles, T. P. et al. Role of intermolecular forces in defining material properties of protein nanofibrils. Science 318, 1900–1903 (2007). 7. Nelson, R. et al. Structure of the cross-beta spine of amyloid-like fibrils. Nature 435, 773–778 (2005). 8. Chiti, F. & Dobson, C. M. Protein misfolding, functional amyloid and human disease. Annu. Rev. Biochem. 75, 333–366 (2006). 9. Dobson, C. M. Protein folding and misfolding. Nature 426, 884–890 (2003).

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Type
research article
DOI
10.1038/nnano.2010.59
Web of Science ID

WOS:000279106500015

Author(s)
Adamcik, Jozef  
Jung, Jin-Mi
Flakowski, Jérôme
De Los Rios, Paolo  
Dietler, Giovanni  
Mezzenga, Raffaele
Date Issued

2010

Publisher

Nature Publishing Group

Published in
Nature Nanotechnology
Volume

5

Issue

6

Start page

423

End page

428

Subjects

amyloid aggregation

•

atomic force microscopy

•

Alzheimer

•

Creutzfeldt–Jakob

•

Huntington

•

Beta-Lactoglobulin Gels

•

Fibril Formation

•

Globular-Proteins

•

Molecules

•

Length

•

Model

Note

PUBLISHED ONLINE: 11 APRIL 2010

Editorial or Peer reviewed

REVIEWED

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LPMV  
Available on Infoscience
May 27, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/50455
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