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We examine the equilibrium configurations of a nematic liquid crystal with an immersed body in two dimensions. A complex variables formulation provides a means for finding analytical solutions in the case of strong anchoring. Local tractions, forces and torques on the body are discussed in a general setting. For weak (finite) anchoring strengths, an effective boundary technique is proposed which is used to determine asymptotic solutions. The energy-minimizing locations of topological defects on the body surface are also discussed. A number of examples are provided, including circular and triangular bodies, and a Janus particle with hybrid anchoring conditions. Analogies to classical results in fluid dynamics are identified, including d'Alembert's paradox, Stokes’ paradox and the Kutta condition for circulation selection. 

We review the literature on swimming in complex fluids. A classification is proposed by comparing the length- and timescales of a swimmer with those of nearby obstacles, interpreted broadly, extending from rigid or soft confining boundaries to molecules that confer the bulk fluid with complex stresses. A third dimension in the classification is the concentration of swimmers, which incorporates fluids whose complexity arises purely by the collective motion of swimming organisms. For each of the eight system types that we identify, we provide a background and describe modern research findings. Although some types have seen a great deal of attention for decades, others remain uncharted waters still open and awaiting exploration. 

Biological membranes are host to proteins and molecules which may form domain-like structures resulting in spatially varying material properties. Vesicles with such heterogeneous membranes can exhibit intricate shapes at equilibrium and rich dynamics when placed into a flow. Under the assumption of small deformations and a two-dimensional system, we develop a reduced-order model to describe the fluid-structure interaction between a viscous background shear flow and an inextensible membrane with spatially varying bending stiffness and spontaneous curvature. Material property variations of a critical magnitude, relative to the flow rate and internal/external viscosity contrast, can set off a qualitative change in the vesicle dynamics. A membrane of nearly constant bending stiffness or spontaneous curvature undergoes a small amplitude swinging motion (which includes tangential tank-treading), while for large enough material variations the dynamics pass through a regime featuring tumbling and periodic phase-lagging of the membrane material, and ultimately for very large material variation to a rigid-body tumbling behaviour. Distinct differences are found for even and odd spatial modes of domain distribution. Full numerical simulations are used to probe the theoretical predictions, which appear valid even when studying substantially deformed membranes. 

Mammalian cells are soft, and correct functioning requires that cells undergo dynamic shape changes in vivo. Although a range of diseases are associated with stiffening of red blood cells (RBCs; e.g., sickle cell anemia or malaria), the mechanical properties and thus shape responses of cells to complex viscoelastic environments are poorly understood. We use vapor pressure measurements to identify aqueous liquid crystals (LCs) that are in osmotic equilibrium with RBCs and explore mechanical coupling between RBCs and LCs. When transferred from an isotropic aqueous phase into a LC, RBCs exhibit complex yet reversible shape transformations, from initially biconcave disks to elongated and folded geometries with noncircular cross-sections. Importantly, whereas the shapes of RBCs are similar in isotropic fluids, when strained by LC, a large variance in shape response is measured, thus unmasking cell-to-cell variation in mechanical properties. Numerical modeling of LC and cell mechanics reveals that RBC shape responses occur at constant cell membrane area but with membrane shear moduli that vary between cells from 2 to 16 × 10⁻⁶N/m. Temperature-dependent LC elasticity permits continuous tuning of RBC strains, and chemical cross-linking of RBCs, a model for diseased cells, leads to striking changes in shape responses of the RBCs. Overall, these results provide insight into the coupling of strain between soft mammalian cells and synthetic LCs, and hint at new methods for rapidly characterizing mechanical properties of single mammalian cells in a population and thus cell-to-cell variance.