• DOI:10.1103/PhysRevE.89.022606
• Corpus ID: 6602914

Dynamics of a semiflexible polymer or polymer ring in shear flow.

@article{Lang2014DynamicsOA,
  title={Dynamics of a semiflexible polymer or polymer ring in shear flow.},
  author={Philipp Lang and Benedikt Obermayer and Erwin Frey},
  journal={Physical review. E, Statistical, nonlinear, and soft matter physics},
  year={2014},
  volume={89 2},
  pages={
          022606
        }
}

• Philipp Lang, B. Obermayer, Erwin Frey
• Published 14 February 2014
• Physics
• Physical review. E, Statistical, nonlinear, and soft matter physics

Polymers exposed to shear flow exhibit a remarkably rich tumbling dynamics. While rigid rods rotate on Jeffery orbits, a flexible polymer stretches and coils up during tumbling. Theoretical results show that in both of these asymptotic regimes the corresponding tumbling frequency f(c) in a linear shear flow of strength γ scales as a power law Wi(2/3) in the Weissenberg number Wi = γτ, where τ is a characteristic time of the polymer's relaxational dynamics. For a flexible polymer these theoretical results are well confirmed by a large body of experimental single molecule studies. However, for the intermediate semiflexible regime, especially relevant for cytoskeletal filaments like F-actin and microtubules, the situation is less clear. While recent experiments on single F-actin filaments are still interpreted within the classical Wi(2/3) scaling law, theoretical results indicated deviations from it. Here we perform extensive Brownian dynamics simulations to explore the tumbling dynamics of semiflexible polymers over a broad range of shear strength and the polymer's persistence length l(p). We find that the Weissenberg number alone does not suffice to fully characterize the tumbling dynamics, and the classical scaling law breaks down. Instead, both the polymer's stiffness and the shear rate are relevant control parameters. Based on our Brownian dynamics simulations we postulate that in the parameter range most relevant for cytoskeletal filaments there is a distinct scaling behavior with f(c) τ* = Wi(3/4)f(c)(x) with Wi = γτ* and the scaling variable x = (l(p)/L)(Wi)(-1/3); here τ* is the time the polymer's center of mass requires to diffuse its own contour length L. Comparing these results with experimental data on F-actin we find that the Wi(3/4) scaling law agrees quantitatively significantly better with the data than the classical Wi(2/3) law. Finally, we extend our results to single ring polymers in shear flow, and find similar results as for linear polymers with slightly different power laws.