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Nano Lett. 2020 Mar 20. doi: 10.1021/acs.nanolett.9b04083. [Epub ahead of print]

Fluctuation-Based Super-Resolution Traction Force Microscopy.

Author information

1
Turku Bioscience Centre, University of Turku and Åbo Akademi University, FI-20520 Turku, Finland.
2
MRC-Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, U.K.
3
The Francis Crick Institute, London NW1 1AT, U.K.
4
Faculty of Science and Engineering, Cell Biology, Åbo Akademi University, 20520 Turku, Finland.
5
Department of Biochemistry, University of Turku, FIN-20520 Turku, Finland.

Abstract

Cellular mechanics play a crucial role in tissue homeostasis and are often misregulated in disease. Traction force microscopy is one of the key methods that has enabled researchers to study fundamental aspects of mechanobiology; however, traction force microscopy is limited by poor resolution. Here, we propose a simplified protocol and imaging strategy that enhances the output of traction force microscopy by increasing i) achievable bead density and ii) the accuracy of bead tracking. Our approach relies on super-resolution microscopy, enabled by fluorescence fluctuation analysis. Our pipeline can be used on spinning-disk confocal or widefield microscopes and is compatible with available analysis software. In addition, we demonstrate that our workflow can be used to gain biologically relevant information and is suitable for fast long-term live measurement of traction forces even in light-sensitive cells. Finally, using fluctuation-based traction force microscopy, we observe that filopodia align to the force field generated by focal adhesions.

KEYWORDS:

Fluctuation-based super-resolution microscopy; SACD; SRRF; live imaging; mechanobiology; traction force microscopy

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