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| Main Authors: | , , |
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| Format: | Preprint |
| Published: |
2025
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2510.15771 |
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Table of Contents:
- Active transport of biomolecular condensates and cell migration in collectives are fundamental to development, homeostasis, and processes such as cancer progression, wound healing, and infection response. Yet how these assemblies are positioned, regulated, and driven through cycles of dissolution and reassembly is not fully understood. We address this using a model of attractive active Brownian particles (ABPs). Using Brownian dynamics simulations, we show that these particles undergo liquid-gas phase separation, and spatially varying activity fields induce striking emergent dynamics. Droplets migrate up activity gradients, and above a critical activity, they fragment into a gas phase. The gas then migrates down the gradient, and droplets reassemble, yielding robust positioning cycles. This emergent condensate cycle arises without biochemical feedback loops and relies only on the interplay of attractions, motility, and gradients. In binary mixtures of active-passive particles, differential cohesion leads to self-sorting of particles, where strongly-cohesive ABPs compact into dense cores surrounded by peripheries enriched with weakly-cohesive passive particles. The passive particles stabilize the dynamic clusters of ABPs, and they migrate toward high-activity regions. Our findings suggest a generic mechanism for spatial control and turnover of condensates in biology.