Affiliation:
1. Department of Physics and Astronomy, University of Southern California, Los Angeles, CA 90089
2. Department of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089
3. Laboratory of Molecular Neurobiology and Biophysics, The Rockefeller University, New York, NY 10065
4. HHMI, The Rockefeller University, New York, NY 10065
Abstract
We show in the companion paper that the free membrane shape of lipid bilayer vesicles containing the mechanosensitive ion channel Piezo can be predicted, with no free parameters, from membrane elasticity theory together with measurements of the protein geometry and vesicle size [C. A. Haselwandter, Y. R. Guo, Z. Fu, R. MacKinnon,
Proc. Natl. Acad. Sci. U.S.A.
, 10.1073/pnas.2208027119 (2022)]. Here we use these results to determine the force that the Piezo dome exerts on the free membrane and hence, that the free membrane exerts on the Piezo dome, for a range of vesicle sizes. From vesicle shape measurements alone, we thus obtain a force–distortion relationship for the Piezo dome, from which we deduce the Piezo dome’s intrinsic radius of curvature,
42
±
12
nm, and bending stiffness,
18
±
2.1
k
B
T
, in freestanding lipid bilayer membranes mimicking cell membranes. Applying these estimates to a spherical cap model of Piezo embedded in a lipid bilayer, we suggest that Piezo’s intrinsic curvature, surrounding membrane footprint, small stiffness, and large area are the key properties of Piezo that give rise to low-threshold, high-sensitivity mechanical gating.
Publisher
Proceedings of the National Academy of Sciences
Cited by
19 articles.
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