Olivia du Roure, PMMH

Olivia du Roure, Anke Lindner, Ehssan Nazockdast and Michael Shelley

Annual Review of Fluid Mechanics (2019) Vol. 51:539-572.

The dynamics and deformations of immersed flexible fibers are at the heart of important industrial and biological processes, induce peculiar mechanical and transport properties in the fluids that contain them, and are the basis for novel methods of flow control. Here we focus on the low–Reynolds number regime where advances in studying these fiber–fluid systems have been especially rapid. On the experimental side, this is due to new methods of fiber synthesis, microfluidic flow control, and microscope-based tracking measurement techniques. Likewise, there have been continuous improvements in the specialized mathematical modeling and numerical methods needed to capture the interactions of slender flexible fibers with flows, boundaries, and each other.

Joseph Tavacoli, Julien Heuvingh, and Olivia du Roure (2017)

Materials in Special Issue ”Designed Colloidal Self-Assembly”, 10, 1291.

In this communication we outline how the bespoke arrangements and design of micron-sized superparamagnetic shapes provide levers to modulate their assembly under homogeneous magnetic fields. We label this new approach, ‘assembly modulated by particle position and shape’ (APPS). Specifically, using rectangular lattices of superparamagnetic micron-sized cuboids, we construct distinct microstructures by adjusting lattice pitch and angle of array with respect to a magnetic field. Broadly, we find two modes of assembly: (1) immediate 2D jamming of the cuboids as they rotate to align with the applied field (rotation-induced jamming) and (2) aggregation via translation after their full alignment (dipole-dipole assembly). The boundary between these two assembly pathways is independent on field strength being solely a function of the cuboid’s dimensions, lattice pitch, and array angle with respect to field—a relationship which we capture, along with other features of the assembly process, in a ‘phase diagram’. In doing so, we set out initial design rules to build custom made assemblies. Moreover, these assemblies can be made flexible thanks to the hinged contacts of their particle building blocks. This flexibility, combined with the superparamagnetic nature of the architectures, renders our assembly method particularly appropriate for the construction of complex actuators at a scale hitherto not possible.

Pierre Bauer, Joseph Tavacoli, Thomas Pujol, Jessica Planade, Julien Heuvingh* and Olivia du Roure* (2017)

Scientific Reports 7: 15688 | DOI:10.1038/s41598-017-15638-5.

We measured mechanical properties and dynamic assembly of actin networks with a new method based on magnetic microscopic cylinders. Dense actin networks are grown from the cylinders’ surfaces using the biochemical Arp2/3-machinery at play in the lamellipodium extension and other force-generating processes in the cell. Under a homogenous magnetic field the magnetic cylinders self-assemble into chains in which forces are attractive and depend on the intensity of the magnetic field. We show that these forces, from piconewtons to nanonewtons, are large enough to slow down the assembly of dense actin networks and controlled enough to access to their non linear mechanical responses. Deformations are measured with nanometer-resolution, well below the optical resolution. Self-assembly of the magnetic particles into chains simplifies experiments and allows for parallel measurements. The combination of accuracy and good throughput of measurements results in a method with high potential for cell and cytoskeleton mechanics. Using this method, we observed in particular a strong non linear mechanical behavior of dense branched actin networks at low forces that has not been reported previously.

Tavacoli, J., Brown, A., Bauër, P., du Roure, O., & Heuvingh, J.

RSC Advances, 6(67), 62624–62629.

We report the spontaneous formation of rings when a colloidal dispersion, containing silica-coated iron-oxide particles and the liquids ethanol and ethoxylated trimethylolpropane triacrylate, is deposited within micron-sized PDMS wells. Just after filling, the interface between air and the dispersion is a meniscus dictated by the dispersion’s contact angle on PDMS. Upon evaporation of ethanol the meniscus lowers and, if a critical volume is reached, a rupture process is initiated and the dispersion adopts a ring morphology. The final dispersion consists only of particles and ethoxylated trimethylolpro- pane triacrylate that can be reticulated to solidify the ring geometry. The colloidal particles within the dispersion are essential for the stability of the rings prior to the reticulation. Here, by using iron-oxide based colloidal particles we fabricated superparamagnetic rings, opening up newavenues for applications. The dimensions of the rings can be tuned by adjusting both the size of the PDMS wells and the amount of ethanol in the dispersion. In this manner it is possible to fabricate rings with annuli smaller than a micron – a scale below the lower limit of standard lithography. Calculations assuming an equilibrium contact angle of ethoxylated trimethylolpropane triacrylate on PDMS reproduce the experimental results strikingly well.

Brangbour, C., du Roure, O., Helfer, E., Démoulin, D., Mazurier, A., Fermigier, M., Carlier, M.-F., Jérôme Bibette et Jean Baudry

PLoS Biology, 2011, 9(4), e1000613. doi :10.1371/journal.pbio.1000613

Pujol, T., du Roure, O., Fermigier, M., and Heuvingh, J.

Proceedings of the National Academy of Sciences, 2012, 109(26), 10364–10369.

Actin filaments play a fundamental role in cell mechanics: assembled into networks by a large number of partners, they ensure cell integrity, deformability, and migration. Here we focus on the mechanics of the dense branched network found at the leading edge of a crawling cell. We develop a new technique based on the dipolar attraction between magnetic colloids to measure mechanical properties of branched actin gels assembled around the colloids. This technique allows us to probe a large number of gels and, through the study of different networks, to access fundamental relationships between their microscopic structure and their mechanical properties. We show that the architecture does regulate the elasticity of the network: increasing both capping and branching concentrations strongly stiffens the networks. These effects occur at protein concentrations that can be regulated by the cell. In addition, the dependence of the elastic modulus on the filaments’ flexibility and on increasing internal stress has been studied. Our overall results point toward an elastic regime dominated by enthalpic rather than entropic deformations. This result strongly differs from the elasticity of diluted cross-linked actin networks and can be explained by the dense dendritic structure of lamellipodium-like networks.