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

Biophys. J. BioFAST: First Published August 11, 2006. doi:10.1529/biophysj.105.079517
© 2006 by the Biophysical Society.


A more recent version of this article appeared on November 1, 2006.
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
biophysj.105.079517v1
91/9/3135    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 Milescu, L. S
Right arrow Articles by Sachs, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Milescu, L. S
Right arrow Articles by Sachs, F.

BIOPHYSICAL THEORY AND MODELING

Extracting dwell time sequences from processive molecular motor data

Lorin S Milescu 1, Ahmet Yildiz 2, Paul Selvin 2 and Frederick Sachs 3*

1 NINDS, NIH
2 UI
3 UB

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

Submitted on December 11, 2005
Revised on January 30, 2006
Accepted on 28 June 2006


   Abstract
Processive molecular motors, such as kinesin, myosin, or dynein, convert chemical energy into mechanical energy by hydrolyzing ATP. The mechanical energy is used for moving in discrete steps along the cytoskeleton and carrying a molecular load. Single molecule recordings of motor position along a substrate polymer appear as a stochastic staircase. Recordings of other single molecules, such as F1-ATPase, RNA polymerase, or topoisomerase have the same appearance. We present a maximum likelihood algorithm that extracts the dwell time sequence from noisy data, and estimates state transition probabilities and the distribution of the motor step size. The algorithm can handle models with uniform or alternating step sizes, and reversible or irreversible kinetics. A periodic Markov model describes the repetitive chemistry of the motor, and a Kalman filter allows to include models with variable step size and to correct for baseline drift. The data are optimized recursively and globally over single or multiple data sets, making the results objective over the full scale of the data. Local binary algorithms, such as the t-test, do not represent the behavior of the whole data set. Our method is model-based, and allows rapid testing of different models by comparing the likelihood scores. From data obtained with current technology, steps as small as 8 nm can be resolved and analyzed with our method. The kinetic consequences of the extracted dwell sequence can be further analyzed in detail. We show results from analyzing simulated and experimental kinesin and myosin motor data. The algorithm is implemented in the free QuB software.

Key Words: FIONA, Markov, idealization, kinesin, likelihood, myosin




This article has been cited by other articles:


Home page
Biophys. JHome page
B. C. Carter, M. Vershinin, and S. P. Gross
A Comparison of Step-Detection Methods: How Well Can You Do?
Biophys. J., January 1, 2008; 94(1): 306 - 319.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
M. Linden and M. Wallin
Dwell Time Symmetry in Random Walks and Molecular Motors
Biophys. J., June 1, 2007; 92(11): 3804 - 3816.
[Abstract] [Full Text] [PDF]




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