Below are brief highlights from recent work:
Below are brief highlights from recent work:
Torsional elasticity strongly shapes how a semiflexible helical polymer packs into and ejects from a confined capsid. Mild torsional rigidity speeds up packing, while higher stiffness first slows and then accelerates it due to competition between spooling and increased persistence length—a feature that disappears without confinement. Torsional stiffness also promotes spool-like structures, whereas ejection slows monotonically as rigidity impedes uncoiling. Overall, torsional mechanics critically influence both packing and release in confined polymers such as viral DNA.
Erythrocyte sedimentation arises from the collapse of a soft-particle gel formed by densely packed, deformable red blood cells with weak attractions. Experiments, simulations, and theory show that stronger fibrinogen-mediated interactions create a more porous, permeable cell network, leading to faster sedimentation. Together, these results support a gel-based mechanism rather than sedimentation of disjoint aggregates and link ESR directly to the microstructure of the erythrocyte network.
Malaria parasites align their apex to the red blood cell (RBC) membrane through a passive process driven by stochastic adhesion bonds and RBC deformability. Simulations show that membrane deformation helps wrap the parasite and promotes apex contact, while increased RBC rigidity drastically slows alignment. Parasite shape also matters: the native egg-like form achieves reliably fast alignment across a wide range of adhesion strengths and membrane rigidities, whereas spherical, oblate, or highly elongated shapes often align more slowly. Overall, parasite adhesion, RBC mechanics, and shape jointly govern the efficiency of apical alignment required for successful invasion.
Refs: eLife (2020)