SearcharxivSearch

arXiv · 2512.03609

Hamiltonian Active Particles in Incompressible Fluid Membranes

Abstract

Active proteins and membrane-bound motors exert force dipole flows along fluid interfaces and lipid bilayers. We develop a Hamiltonian framework for the interactions of pusher and puller dipoles embedded in an \emph{incompressible} two-dimensional membrane supported by a shallow viscous subphase. Beginning from the Brinkman-regularized Stokes equations of the membrane-subphase system, we construct the near-field and far-field dipolar velocity fields and associated stream functions. For two quenched (fixed orientation) dipoles, we obtain exact analytic solutions in both the near- and far-field regimes. Although generic dipoles reorient under local membrane vorticity, we show that the far-field dipolar flow is vorticity-free; force-free motors therefore retain fixed orientations and obey a position-based Hamiltonian dynamics in which the positions of $N$ dipoles evolve via an effective Hamiltonian built from the dipolar stream function. In the near field, where the flow possesses finite vorticity, a Hamiltonian formulation is recovered in the quenched-orientation limit. For identical dipoles, the far-field Hamiltonian produces rapid clustering from random initial conditions, whereas the near-field Hamiltonian suppresses collapse leading to non-aggregating configurations. The phase portraits reveal that the many-body collapse observed in the time evolution of the far field Hamiltonian arises from angular transport across phase space enabled by the screened hydrodynamic interaction. Our work thus provides a concrete realization of a position-based Hamiltonian formulation for active particles in incompressible fluid membranes and shows that hydrodynamic screening can reorganize both the dynamical phase space and the collective organization of active dipoles.

Explore related subjects

Keep this discovery

BibTeXRIS

Sneha Krishnan, Rickmoy Samanta. 2025-12-03. Hamiltonian Active Particles in Incompressible Fluid Membranes. https://doi.org/10.1103/v4kq-784w

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Slow Dynamics and the Geometry of Jammed Packings

Saddle points in the energy landscape of granular packings dominate the discrete steepest descent dynamics and ultimately determine the path that an out of mechanical equilibrium packing will follow and the resulting stable minimum that it will find. The saddle points that ultimately determine the resulting minima tend to be low-index saddle points. For models with an analytic energy landscape, such as the $p$-spin model, the steepest descent minimization path is affected by higher-index saddle points, which pull the system towards saddle points of decreasing index before arriving at the minima. Here, we examine the steepest descent minimization path of granular packings and compare them to the $p$-spin model. We show that the granular packing steepest descent minimization paths act like their smooth energy landscape counterparts and get attracted by saddle points. The index versus time curves for all models follow a shifted, stretched exponential. We further show that the shape parameter for the granular packings is unchanged when the energy landscape is modified to become analytic (Gaussian potential in a harmonic well) or non-local (Mari-Krzakala-Kurchan). The $p$-spin, on the other hand, has a significantly larger shape parameter. The reason is not due to the dimensionality, packing fraction, nonanalyticity, or the locality of the Hamiltonian of the models. The exact reason for the discrepancy in the shape parameter is \st{still} an unsolved mystery.

cond-mat.soft

A Phase-Field Study of Desiccation Crack Pattern Maturation under Drying-Wetting Cycles

The characteristic intersection angle of the desiccation crack relaxes from near \ang{90} toward \ang{120} under repeated drying--wetting cycles. However, the theoretical understanding of this relaxation is insufficient, especially the modeling of the drying--wetting cycles. Here we introduce a phase-field model of desiccation fracture, extending the model proposed in previous studies by adding crack healing and a scar effect left by past cracks. By repeating drying--wetting cycles in a finite element simulation, we find that the angle distribution develops a growing peak near \ang{120} as the cycle number increases, consistent with experiments. The standard deviation of the intersection angle from \ang{120} relaxes exponentially with a characteristic time of about 2.85 cycles. These results are consistent with experiments, except that the characteristic time is slightly smaller than the experimental value. Crack energy dominates the total energy and also relaxes exponentially with nearly the same characteristic cycle as the angle relaxation. This decay is driven mainly by a shortening of the effective crack length rather than a change in effective fracture toughness.

cond-mat.soft

Kinetics of ferritin crystal formation and melting in acoustically levitated droplets

Understanding protein crystallization pathways is essential for controlling crystallization in structural biology, materials science, and pharmaceutical applications. Classical nucleation theory does not fully capture crystallization processes for several proteins, including ferritin. Here, we combine acoustic levitation with small- and wide-angle X-ray scattering (SAXS and WAXS) to monitor ferritin crystallization in evaporating aqueous polyethylene glycol (PEG) solutions. Acoustic levitation rapidly drives the droplets through a broad range of protein and polymer concentrations, enabling time-resolved measurements of crystallization during evaporation. The scattering data show that ferritin crystals form during evaporation and subsequently lose their crystalline order upon further dehydration. Varying the PEG molecular weight switches between distinct crystallization pathways: one dominated by attractive protein-protein interactions and another dominated by repulsive interactions and excluded-volume effects. Furthermore, we find that lower molecular weight PEG (1000 g/mol) suppresses the dehydration-induced loss of crystalline order observed for higher molecular weight PEG (6000 g/mol), providing a simple strategy for improving protein crystal stability.

cond-mat.soft