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The stretching force on a tethered polymer in pressure-driven flow
Kai Szuttor1, Tamal Roy2, Steffen Hardt2
1Institute for Computational Physics, University of Stuttgart, Allmandring 3, D-70569 Stuttgart, Germany.
The Journal of Chemical Physics
|July 24, 2017
Summary
We studied polymer stretching in microchannels using simulations. Our findings show polymer extension depends linearly on channel flow, aligning chains along walls, matching experimental DNA stretching data.
Area of Science:
- Polymer physics
- Fluid dynamics
- Computational biophysics
Background:
- Understanding polymer behavior in confined geometries is crucial for microfluidic and nanofluidic applications.
- Tethered polymer stretching is influenced by fluid flow and channel dimensions.
Purpose of the Study:
- To investigate the stretching dynamics of a single tethered polymer in micro- and nanochannels.
- To establish a relationship between fluid flow properties and the stretching force on the polymer chain.
- To compare simulation results with experimental data for tethered DNA.
Main Methods:
- Mesoscopic lattice-Boltzmann/molecular dynamics simulations were employed.
- Analytical expressions for stretching force were derived and validated.
- Langevin dynamics simulations were used to confirm findings.
- Microfluidic stretching experiments of tethered λ-DNA provided comparative data.
Main Results:
- A proposed analytical expression for stretching force shows linear dependence on monomer count and boundary shear rate.
- Hydrodynamic interactions were found to have negligible influence on polymer stretching.
- Simulation data accurately predict fractional polymer chain extension.
- Weak Poiseuille flow profiles effectively align polymer chains along channel walls.
Conclusions:
- The study provides a validated analytical model for tethered polymer stretching in micro/nanochannels.
- Simulation results align well with experimental observations of DNA stretching.
- Findings offer insights into polymer behavior under flow in confined environments.
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