Directly examining subcellular mechanics whilst avoiding excessive strain of a live cell requires the precise control of light stress on very small areas, which is fundamentally difficult. Here we use a glass nanopipet out of contact with the plasma membrane to both exert the stress on the cell and also accurately monitor cellular compression. This allows the mapping of cell stiffness at a lateral resolution finer than 100 nm. We calculate the stress a nanopipet exerts on a cell as the sum of the intrinsic pressure between the tip face and the plasma membrane plus its direct pressure on any glycocalyx, both evaluated from the gap size in terms of the ion current decrease. A survey of cell types confirms that an intracellular pressure of approximately 120 Pa begins to detach the plasma membrane from the cytoskeleton and reveals that the first 660 +/- 90 nm of compression of a neuron cell body is much softer than previous methods have been able to detect.
@article{arxiv.2103.03811,
title = {Low Stress Ion Conductance Microscopy of Sub-Cellular Stiffness},
author = {Richard W. Clarke and Pavel Novak and Alexander Zhukov and Eleanor J. Tyler and Marife Cano-Jaimez and Anna Drews and Owen Richards and Kirill Volynski and Cleo Bishop and David Klenerman},
journal= {arXiv preprint arXiv:2103.03811},
year = {2021}
}