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arXiv · 0904.2704

Stress relaxation microscopy (STREM): Imaging mechanical force decay in cells

Susana Moreno-Flores·Rafael Benitez·Maria dM Vivanco·Jose Luis Toca-Herrera
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Abstract

We have developed a novel scanning probe-based methodology to study cell biomechanics. The time dependence of the force exerted by the cell surface on a scanning probe at constant local deformation has been used to extract local relaxational responses. The generalized Maxwell viscoelastic model that accounts for multi relaxations fully describes the mechanical behaviour of the cell surface that exhibits a bimodal relaxation. Within the range of tested forces (0.1-4 nN) a slow and a fast relaxation with characteristic times of 0.1 and 1s have been detected and assigned to rearrangements in the cell membrane and cytoskeleton cortex, respectively. Relaxation time mapping allows to simultaneously detect non-uniformities in membrane and cytoskeletal mechanical behaviour and can be used as both identifying and diagnosing tools for cell type and cell disease.

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Susana Moreno-Flores, Rafael Benitez, Maria dM Vivanco, Jose Luis Toca-Herrera. 2009-04-17. Stress relaxation microscopy (STREM): Imaging mechanical force decay in cells. https://arxiv.org/abs/0904.2704

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