help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

Biophys. J. BioFAST: First Published January 27, 2006. doi:10.1529/biophysj.105.074211
© 2006 by the Biophysical Society.


A more recent version of this article appeared on April 15, 2006.
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
biophysj.105.074211v1
90/8/2673    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Stukalin, E. B
Right arrow Articles by Kolomeisky, A. B
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stukalin, E. B
Right arrow Articles by Kolomeisky, A. B

BIOPHYSICAL THEORY AND MODELING

ATP hydrolysis stimulates large length fluctuations in single actin filaments

Evgeny B Stukalin 1 and Anatoly B Kolomeisky 1*

1 Rice University

* To whom correspondence should be addressed. E-mail: tolya{at}rice.edu.

Submitted on September 9, 2005
Revised on October 14, 2005
Accepted on 19 December 2005


   Abstract
Polymerization dynamics of single actin filaments is investigated theoretically using a stochastic model that takes into account the hydrolysis of ATP-actin subunits, the geometry of actin filament tips, the lateral interactions between the monomers as well as the processes at both ends of the polymer. Exact analytical expressions are obtained for the mean growth velocity, for the dispersion in the length fluctuations, and the nucleotide composition of the actin filaments. It is found that the ATP hydrolysis has a strong effect on dynamic properties of single actin filaments. At high concentrations of free actin monomers the mean size of the unhydrolyzed ATP-cap is very large, and the dynamics is governed by association/dissociation of ATP-actin subunits. However, at low concentrations the size of the cap becomes finite, and the dissociation of ADP-actin subunits makes a significant contribution to overall dynamics. Actin filament length fluctuations reach a sharp maximum at the boundary between two dynamic regimes, and this boundary is always larger than the critical concentration for the actin filament's growth at the barbed end, assuming the sequential release of phosphate. Random and sequential mechanisms of hydrolysis are compared, and it is found that they predict qualitatively similar dynamic properties at low and high concentrations of free actin monomers with some deviations near the critical concentration. The possibility of attachment and detachment of oligomers in actin filament's growth is also discussed. Our theoretical approach is successfully applied to analyze the latest experiments on the growth and length fluctuations of individual actin filaments.

Key Words: ATP hydrolysis, actin filament growth




This article has been cited by other articles:


Home page
Biophys. JHome page
Y. Lan and G. A. Papoian
The Stochastic Dynamics of Filopodial Growth
Biophys. J., May 15, 2008; 94(10): 3839 - 3852.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
J. Roland, J. Berro, A. Michelot, L. Blanchoin, and J.-L. Martiel
Stochastic Severing of Actin Filaments by Actin Depolymerizing Factor/Cofilin Controls the Emergence of a Steady Dynamical Regime
Biophys. J., March 15, 2008; 94(6): 2082 - 2094.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2006 by the Biophysical Society.