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Published online
doi:10.1083/jcb.200809166
The Journal of Cell Biology, Vol. 185, No. 5, 769-777
The Rockefeller University Press, 0021-9525 $30.00
© Çolakoglu et al.
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Intermediate filaments exchange subunits along their length and elongate by end-to-end annealing



Gülsen Çolakoglu1,2 and Anthony Brown1,2

1 Center for Molecular Neurobiology and 2 Department of Neuroscience, The Ohio State University, Columbus, OH 43210

Correspondence to Anthony Brown: brown.2302{at}osu.edu

Actin filaments and microtubules lengthen and shorten by addition and loss of subunits at their ends, but it is not known whether this is also true for intermediate filaments. In fact, several studies suggest that in vivo, intermediate filaments may lengthen by end-to-end annealing and that addition and loss of subunits is not confined to the filament ends. To test these hypotheses, we investigated the assembly dynamics of neurofilament and vimentin intermediate filament proteins in cultured cells using cell fusion, photobleaching, and photoactivation strategies in combination with conventional and photoactivatable fluorescent fusion proteins. We show that neurofilaments and vimentin filaments lengthen by end-to-end annealing of assembled filaments. We also show that neurofilaments and vimentin filaments incorporate subunits along their length by intercalation into the filament wall with no preferential addition of subunits to the filament ends, a process which we term intercalary subunit exchange.


Abbreviations used in this paper: NFH, neurofilament protein H; NFL, neurofilament protein L; NFM, neurofilament protein M; PAGFP, photoactivatable GFP; PEG, polyethylene glycol; ULF, unit length filament.

© 2009 Çolakoglu and Brown
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