article · 28/11/2015
Non-Markovian closure kinetics of flexible polymers with hydrodynamic interactions
Résumé
This paper presents a theoretical analysis of the closure kinetics of a polymer with hydrodynamic interactions. This analysis, which takes into account the non-Markovian dynamics of the end-to-end vector and relies on the preaveraging of the mobility tensor (Zimm dynamics), is shown to reproduce very accurately the results of numerical simulations of the complete nonlinear dynamics. It is found that Markovian treatments based on a Wilemski-Fixman approximation significantly overestimate cyclization times (up to a factor 2), showing the importance of memory effects in the dynamics. In addition, this analysis provides scaling laws of the mean first cyclization time (MFCT) with the polymer size N and capture radius b, which are identical in both Markovian and non-Markovian approaches. In particular, it is found that the scaling of the MFCT for large N is given by T similar to N-3/2 ln(N/b(2)), which differs from the case of the Rouse dynamics where T similar to N-2. The extension to the case of the reaction kinetics of a monomer of a Zimm polymer with an external target in a confined volume is also presented. (C) 2015 AIP Publishing LLC.
Citer cet article
Levernier, N., Dolgushev, M., Benichou, O., Blumen, A., Guerin, T., & Voituriez, R. (2015). Non-Markovian closure kinetics of flexible polymers with hydrodynamic interactions. JOURNAL OF CHEMICAL PHYSICS, 143(20). https://doi.org/10.1063/1.4935966
@article{Levernier2015_187,
author = {Levernier, N. and Dolgushev, M. and Benichou, O. and Blumen, A. and Guerin, T. and Voituriez, R.},
year = {2015},
month = {11},
title = {Non-Markovian closure kinetics of flexible polymers with hydrodynamic interactions},
journal = {JOURNAL OF CHEMICAL PHYSICS},
volume = {143},
number = {20},
abstract = {This paper presents a theoretical analysis of the closure kinetics of a polymer with hydrodynamic interactions. This analysis, which takes into account the non-Markovian dynamics of the end-to-end vector and relies on the preaveraging of the mobility tensor (Zimm dynamics), is shown to reproduce very accurately the results of numerical simulations of the complete nonlinear dynamics. It is found that Markovian treatments based on a Wilemski-Fixman approximation significantly overestimate cyclization times (up to a factor 2), showing the importance of memory effects in the dynamics. In addition, this analysis provides scaling laws of the mean first cyclization time (MFCT) with the polymer size N and capture radius b, which are identical in both Markovian and non-Markovian approaches. In particular, it is found that the scaling of the MFCT for large N is given by T similar to N-3/2 ln(N/b(2)), which differs from the case of the Rouse dynamics where T similar to N-2. The extension to the case of the reaction kinetics of a monomer of a Zimm polymer with an external target in a confined volume is also presented. (C) 2015 AIP Publishing LLC.},
url = {http://www.dx.doi.org/10.1063/1.4935966},
doi = {10.1063/1.4935966},
issn = {0021-9606},
}
TY - JOUR
AU - Levernier, N.
AU - Dolgushev, M.
AU - Benichou, O.
AU - Blumen, A.
AU - Guerin, T.
AU - Voituriez, R.
PY - 2015
DA - 2015/11/28
TI - Non-Markovian closure kinetics of flexible polymers with hydrodynamic interactions
JO - JOURNAL OF CHEMICAL PHYSICS
VL - 143
IS - 20
SN - 0021-9606
AB - This paper presents a theoretical analysis of the closure kinetics of a polymer with hydrodynamic interactions. This analysis, which takes into account the non-Markovian dynamics of the end-to-end vector and relies on the preaveraging of the mobility tensor (Zimm dynamics), is shown to reproduce very accurately the results of numerical simulations of the complete nonlinear dynamics. It is found that Markovian treatments based on a Wilemski-Fixman approximation significantly overestimate cyclization times (up to a factor 2), showing the importance of memory effects in the dynamics. In addition, this analysis provides scaling laws of the mean first cyclization time (MFCT) with the polymer size N and capture radius b, which are identical in both Markovian and non-Markovian approaches. In particular, it is found that the scaling of the MFCT for large N is given by T similar to N-3/2 ln(N/b(2)), which differs from the case of the Rouse dynamics where T similar to N-2. The extension to the case of the reaction kinetics of a monomer of a Zimm polymer with an external target in a confined volume is also presented. (C) 2015 AIP Publishing LLC.
DO - 10.1063/1.4935966
UR - http://www.dx.doi.org/10.1063/1.4935966
ER -