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Published on: October 24, 2017
Phase behavior of crowded like-charged mixed polyelectrolytes in a cell-sized sphere
Makiko Negishi1, Masatoshi Ichikawa, Masahiro Nakajima
1Department of Physics, Graduate School of Science, Kyoto University, Kyoto, Japan.
Giant DNA and alginate mixtures show unique phase behavior within cell-sized spheres. Sphere size dictates polymer distribution, unlike homogeneous bulk solutions, due to surface-to-volume effects.
Area of Science:
- Polymer Physics
- Biophysics
- Materials Science
Background:
- Semiflexible polyelectrolytes like giant DNA and alginate are crucial in biological systems.
- Understanding polymer behavior in confined environments is essential for cell biology and nanotechnology.
- Crowded conditions and confinement significantly alter polymer phase behavior compared to bulk solutions.
Purpose of the Study:
- To investigate the phase behavior of a mixture of giant DNA and alginate under crowded conditions within cell-sized spheres.
- To determine how sphere size influences the spatial distribution and phase separation of these polyelectrolytes.
- To elucidate the role of surface-to-volume effects in confined polymer systems.
Main Methods:
- Microscopic observation of polymer mixtures in spheres ranging from 5-40 μm in diameter.
- Utilizing the Flory-Huggins model with a novel curvature-dependent interaction term.
- Comparing phase behavior in confined spheres to that of bulk solutions.
Main Results:
- The polymer mixture exhibited homogeneous and isotropic behavior in bulk solution.
- In small spheres, giant DNA was completely depleted from the surface.
- In medium-sized spheres, partial depletion of giant DNA from the surface was observed, with the remainder staying within the sphere.
Conclusions:
- The phase behavior of giant DNA and alginate mixtures is strongly dependent on the size of the confining sphere.
- Surface-to-volume effects, particularly the curvature-dependent interaction, govern the observed phase separation.
- This study provides insights into polymer behavior in cellular microenvironments and confined geometries.
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