- Open Access
Mechanical stress induced by the polymerization of an active gel near a surface
Phys. Rev. Research 8, 033308 – Published 14 September, 2026
DOI: https://doi.org/10.1103/6nx5-yg9j
Abstract
Actin flow in the cortical cytoskeleton underneath the cell membrane generates mechanical stresses that shape the cell surface. We study this mechanism using a hydrodynamic model of a compressible active gel polymerizing at the membrane and undergoing turnover. We determine how actin flow, density relaxation, and friction of actin with the membrane generate stress on a corrugated membrane at the linear order in deformation. Analytical solutions in limiting regimes, combined with finite element methods in the general case, provide a map of normal and tangential stresses as functions of compressibility, interfacial friction, and actin turnover, and determine the conditions under which actin polymerization can render the membrane linearly unstable. The nonlinear regime is also briefly discussed.
Physics Subject Headings (PhySH)
Article Text
References (22)
- G. Salbreux, G. Charras, and E. Paluch, Actin cortex mechanics and cellular morphogenesis, Trends Cell Biol. 22, 536 (2012).
- K. Mihali, D. Wörthmüller, and P. Sens, Curvature instability of an active gel growing on a wavy membrane, Phys. Rev. Lett. 136, 258401 (2026).
- H. Zhao, A. Pykäläinen, and P. Lappalainen, I-BAR domain proteins: Linking actin and plasma membrane dynamics, Curr. Opin. Cell Biol. 23, 14 (2011).
- N. Levernier and K. Kruse, Spontaneous formation of chaotic protrusions in a polymerizing active gel layer, New J. Phys. 22, 013003 (2020).
- J. Xu, A. Palmer, and D. Wirtz, Rheology and microrheology of semiflexible polymer solutions: Actin filament networks, Macromolecules 31, 6486 (1998).
- E. Fischer-Friedrich, Y. Toyoda, C. J. Cattin, D. J. Müller, A. A. Hyman, and F. Jülicher, Rheology of the active cell cortex in mitosis, Biophys. J. 111, 589 (2016).
- F. Jülicher, K. Kruse, J. Prost, and J.-F. Joanny, Active behavior of the cytoskeleton, Phys. Rep. 449, 3 (2007).
- J.-F. Joanny, K. Kruse, J. Prost, and S. Ramaswamy, The actin cortex as an active wetting layer, Eur. Phys. J. E 36, 52 (2013).
- H.-Y. Lou, W. Zhao, X. Li, L. Duan, A. Powers, M. Akamatsu, F. Santoro, A. F. McGuire, Y. Cui, D. G. Drubin, and B. Cui, Membrane curvature underlies actin reorganization in response to nanoscale surface topography, Proc. Natl. Acad. Sci. USA 116, 23143 (2019).
- F. Tsai, J. M. Henderson, Z. Jarin, E. Kremneva, Y. Senju, J. Pernier, O. Mikhajlov, J. Manzi, K. Kogan, C. Le Clainche, P. Lappalainen, and P. Bassereau, Activated I-BAR IRSp53 clustering controls the formation of VASP-actin-based membrane protrusions, Sci. Adv. 8, eabp8677 (2022).
- W. Helfrich, Elastic properties of lipid bilayers: Theory and possible experiments, Z. Naturforsch. C 28, 693 (1973).
- M. Fritzsche, A. Lewalle, T. Duke, K. Kruse, and G. Charras, Analysis of turnover dynamics of the submembranous actin cortex, Mol. Biol. Cell 24, 757 (2013).
- J. R. Kuhn and T. D. Pollard, Real-time measurements of actin filament polymerization by total internal reflection fluorescence microscopy, Biophys. J. 88, 1387 (2005).
- T. D. Pollard and G. G. Borisy, Cellular motility driven by assembly and disassembly of actin filaments, Cell 112, 453 (2003).
- P. Bieling, H. T. Li, and M. P. Mullins, Force feedback controls motor activity and mechanical properties of self-assembling branched actin networks, Cell 164, 115 (2016).
- G. T. Charras, M. Coughlin, T. J. Mitchison, and L. Mahadevan, Life and times of a cellular bleb, Biophys. J. 94, 1836 (2008).
- A. Cordes, H. Witt, A. Gallemí-Pérez, B. Brückner, F. Grimm, M. Vache, T. Oswald, J. Bodenschatz, D. Flormann, F. Lautenschläger, M. Tarantola, and A. Janshoff, Prestress and area compressibility of actin cortices determine the viscoelastic response of living cells, Phys. Rev. Lett. 125, 068101 (2020).
- A. Zgorski, R. W. Pastor, and E. Lyman, Surface shear viscosity and interleaflet friction from nonequilibrium simulations of lipid bilayers, J. Chem. Theory Comput. 15, 6471 (2019).
- J. E. Fitzgerald, R. M. Venable, R. W. Pastor, and E. R. Lyman, Surface viscosities of lipid bilayers determined from equilibrium molecular dynamics simulations, Biophys. J. 122, 1094 (2023).
- https://github.com/dworthmuller/ActinWavyMembrane.
- A. Shamanskiy and B. Simeon, Mesh deformation techniques in fluid-structure interaction: Robustness, accumulated distortion and computational efficiency, Computational Mechanics 67, 583 (2021).
- J. Donea, A. Huerta, J.-P. Ponthot, and A. Rodríguez-Ferran, Arbitrary Lagrangian–Eulerian methods, in Encyclopedia of Computational Mechanics, edited by E. Stein, R. Borst, and T. J. R. Hughes (John Wiley & Sons, Ltd., Chichester, UK, 2004), Chap. 14.