Stiffness of Confinement Controls the Localization of an Object under Crowding: Macroscale Real-World and Microscale Numerical Modelings on the Specificity of Intracellular Positioning

Macroscopic systems that mimic microscopic systems can provide fundamental understanding of how macro-molecules (e.g., cellular organelles) are organized in a confined space. We studied the behavior of a large particle interacting with several small particles confined in dishes with hard/soft boundary conditions under mechanical vibration using a cm-scale model. We also performed a numerical simulation for the micro-scale system under Brownian fluctuation with fluctuation-dissipation, as a simple model of living cellular cytoplastic crowding. Under a hard boundary condition, the large sphere preferred the boundary at low crowding but tended to localize to the interior under high crowding. Conversely, when the boundary was soft, the large sphere localized to the interior under low crowding and tended to migrate near the boundary when crowding increased. Interestingly, numerical modeling reproduced similar results for both the experimental hard and soft boundary conditions. Our models revealed that membrane stiffness can affect the organization of biopolymers within a confined space and may help explain cellular dynamics.

Automated summary

Macroscopic systems mimicking microscopic systems were used to study the organization of macro-molecules in a confined space. Experimental and numerical models showed that the behavior of a large particle interacting with small particles under different boundary conditions is influenced by crowding. Membrane stiffness was found to affect the organization of biopolymers and may play a role in cellular dynamics.