Kinetics of the polymer collapse transition: The role of hydrodynamics

N. Kikuchi, J. F. Ryder, C. M. Pooley, and J. M. Yeomans
Phys. Rev. E 71, 061804 – Published 30 June 2005

Abstract

We investigate numerically the dynamical behavior of a polymer chain collapsing in a dilute solution. The rate of collapse is measured with and without the presence of hydrodynamic interactions. We find that hydrodynamic interactions accelerate polymer collapse. We present a scaling theory describing the physical process responsible for the collapse kinetics. Predicted collapse times in a hydrodynamic (τHN43) and a Brownian heat bath (τBN2) agree well with the numerical results (τHN1.40±0.08 and τBN1.89±0.09) where N denotes chain length. The folding kinetics of Go models of proteins is also examined. We show that for these systems, where many free energy minima compete, hydrodynamics has little effect on the kinetics.

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  • Received 20 September 2004

DOI:https://doi.org/10.1103/PhysRevE.71.061804

©2005 American Physical Society

Authors & Affiliations

N. Kikuchi*, J. F. Ryder, C. M. Pooley, and J. M. Yeomans

  • Rudolf Peierls Centre for Theoretical Physics, 1 Keble Road, Oxford, OX1 3NP, United Kingdom

  • *Now at Institut für Physik, Johannes Gutenberg-Universität Mainz, Staudinger Weg 7, D-55099 Mainz, Germany.
  • Now at Chemical and Petroleum Engineering Department, 1249 Benedum Hall, Pittsburgh, PA 15261, USA.

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Vol. 71, Iss. 6 — June 2005

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