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Mapping nanomechanical properties of live cells using multi-harmonic atomic force microscopy.

Abstract:
The nanomechanical properties of living cells, such as their surface elastic response and adhesion, have important roles in cellular processes such as morphogenesis, mechano-transduction, focal adhesion, motility, metastasis and drug delivery. Techniques based on quasi-static atomic force microscopy techniques can map these properties, but they lack the spatial and temporal resolution that is needed to observe many of the relevant details. Here, we present a dynamic atomic force microscopy method to map quantitatively the nanomechanical properties of live cells with a throughput (measured in pixels/minute) that is ∼10-1,000 times higher than that achieved with quasi-static atomic force microscopy techniques. The local properties of a cell are derived from the 0th, 1st and 2nd harmonic components of the Fourier spectrum of the AFM cantilevers interacting with the cell surface. Local stiffness, stiffness gradient and the viscoelastic dissipation of live Escherichia coli bacteria, rat fibroblasts and human red blood cells were all mapped in buffer solutions. Our method is compatible with commercial atomic force microscopes and could be used to analyse mechanical changes in tumours, cells and biofilm formation with sub-10 nm detail.
Publication status:
Published

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Publisher copy:
10.1038/nnano.2011.186

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Physics
Sub department:
Condensed Matter Physics
Role:
Author


Journal:
Nature nanotechnology More from this journal
Volume:
6
Issue:
12
Pages:
809-814
Publication date:
2011-12-01
DOI:
EISSN:
1748-3395
ISSN:
1748-3387


Language:
English
Keywords:
Pubs id:
pubs:206060
UUID:
uuid:f5483922-7583-46bc-a797-ca229d5c61ae
Local pid:
pubs:206060
Source identifiers:
206060
Deposit date:
2012-12-19
ARK identifier:

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