Chaperone-assisted translocation of a polymer through a nanopore
arXiv:1108.0562 · doi:10.1021/ja204892z
Abstract
Using Langevin dynamics simulations, we investigate the dynamics of chaperone-assisted translocation of a flexible polymer through a nanopore. We find that increasing the binding energy between the chaperone and the chain and the chaperone concentration can greatly improve the translocation probability. Particularly, with increasing the chaperone concentration a maximum translocation probability is observed for weak binding. For a fixed chaperone concentration, the histogram of translocation time has a transition from long-tailed distribution to Gaussian distribution with increasing . rapidly decreases and then almost saturates with increasing binding energy for short chain, however, it has a minimum for longer chains at lower chaperone concentration. We also show that has a minimum as a function of the chaperone concentration. For different , a nonuniversal dependence of on the chain length is also observed. These results can be interpreted by characteristic entropic effects for flexible polymers induced by either crowding effect from high chaperone concentration or the intersegmental binding for the high binding energy.
10 pages, to appear in J. Am. Chem. Soc
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Cited by in corpus (8)
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- Chaperone-assisted translocation of flexible polymers in three dimensions
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- Translocation of stiff polymers through a nanopore driven by binding particles
- Chaperone driven polymer translocation through Nanopore: spatial distribution and binding energy
- Non-equilibrium effects in chaperone-assisted translocation of a stiff polymer
- Effects of interaction between nanopore and polymer on translocation time