Force induced conformational transition in a system of interacting stiff polymer: Application to unfolding
arXiv:0704.3172 · doi:10.1103/PhysRevE.72.052901
Abstract
We consider a stiff polymer chain in poor solvent and apply a force at one end of the chain. We find that by varying the stiffness parameter, polymer undergoes a transition from the globule state to the folded like state. The conformation of folded state mimics the -sheet as seen in titin molecule. Using exact enumeration technique, we study the extension-force and force-temperature diagrams of such a system. Force-temperature diagram shows the re-entrance behaviour for flexible chain. However, for stiff chain this re-entrance behaviour is absent and there is an enhancement in -temperature with the rise of stiffness. We further propose that the internal information about the frozen structure of polymer can be read from the distribution of end-to-end distance which shows saw-tooth like behaviour.
RevTeX v4, 9 pages with 6 eps figures
Cited by in corpus (15)
- Collapse Transition of Two-Dimensional Flexible and Semiflexible Polymers
- Does changing the pulling direction give better insight into biomolecules?
- Effects of Molecular Crowding on stretching of polymers in poor solvent
- Force induced stretched state: Effects of temperature
- Pulling self-interacting polymers in two-dimensions
- Force induced unfolding of bio-polymers in a cellular environment: A model study
- Polymers in crowded environment under stretching force: globule-coil transitions
- Adsorption of Externally Stretched Two-Dimensional Flexible and Semi-flexible Polymers near an Attractive Wall
- Statistical mechanics of a polymer chain attached to the interface of a cone-shaped channel
- Stiffness dependence of critical exponents of semiflexible polymer chains situated on two-dimensional compact fractals
- Residual entropy in a model for the unfolding of single polymer chains
- The 3-dimensional random walk with applications to overstretched DNA and the protein titin
- Self-attractive semiflexible polymers under an external force field
- Theta-polymers in crowded media under the stretching force
- Stretching self-interacting, partially directed, flexible and semi-flexible polymers by an external force