Actin Polymerization Kinetics, Cap Structure, and Fluctuations
Polymerization of actin proteins into dynamic structures is essential to eukaryotic cell life, motivating many in vitro experiments measuring polymerization kinetics of individual filaments. Here, we model these kinetics, accounting for all relevant steps revealed by experiment: polymerization, depo...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 102; no. 24; pp. 8543 - 8548 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
14.06.2005
National Acad Sciences |
Subjects | |
Online Access | Get full text |
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Summary: | Polymerization of actin proteins into dynamic structures is essential to eukaryotic cell life, motivating many in vitro experiments measuring polymerization kinetics of individual filaments. Here, we model these kinetics, accounting for all relevant steps revealed by experiment: polymerization, depolymerization, random ATP hydrolysis, and release of phosphate ( Pi). We relate filament growth rates to the dynamics of ATP-actin and ADP- Pi-actin caps that develop at filament ends. At the critical concentration of the barbed end, Ccrit, we find a short ATP cap and a long fluctuation-stabilized ADP- Picap. We show that growth rates and the critical concentration at the barbed end are intimately related to cap structure and dynamics. Fluctuations in filament lengths are described by the length diffusion coefficient, D. Recently Fujiwara et al. [Fujiwara, I., Takahashi, S., Takaduma, H., Funatsu, T. & Ishiwata, S. (2002) Nat. Cell Biol. 4, 666-673] and Kuhn and Pollard [Kuhn, J. & Pollard, T. D. (2005) Biophys. J. 88, 1387-1402] observed large length fluctuations slightly above Ccrit, provoking speculation that growth may proceed by oligomeric rather than monomeric on-off events. For the single-monomer growth process, we find that D exhibits a pronounced peak below Ccrit, due to filaments alternating between capped and uncapped states, a mild version of the dynamic instability of microtubules. Fluctuations just above Ccritare enhanced but much smaller than those reported experimentally. Future measurements of D as a function of concentration can help identify the origin of the observed fluctuations. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This paper was submitted directly (Track II) to the PNAS office. Author contributions: B.O., D.V., and Q.Y. performed research and wrote the paper. To whom correspondence should be addressed at: Department of Chemical Engineering, Columbia University, 500 West 120th Street, New York, NY 10027. E-mail: bo8@columbia.edu. Edited by Edward D. Korn, National Institutes of Health, Bethesda, MD Abbreviations: MC, Monte Carlo; mon, monomers. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.0501435102 |