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Biophys J, October 1998, p. 2059-2069, Vol. 75, No. 4
Department of Biology, University of North Carolina, Chapel Hill, North Carolina 27599 USA
The dynamics of microtubules in living cells can be seen
by fluorescence microscopy when fluorescently labeled tubulin is microinjected into cells, mixing with the cellular tubulin pool and
incorporating into microtubules. The subsequent fluorescence distribution along microtubules can appear "speckled" in
high-resolution images obtained with a cooled CCD camera
(Waterman-Storer and Salmon, 1997. J. Cell Biol.
139:417-434). In this paper we investigate the origins of these
fluorescent speckles. In vivo microtubules exhibited a random pattern
of speckles for different microtubules and different regions of an
individual microtubule. The speckle pattern changed only after
microtubule shortening and regrowth. Microtubules assembled from
mixtures of labeled and unlabeled pure tubulin in vitro also exhibited
fluorescent speckles, demonstrating that cellular factors or organelles
do not contribute to the speckle pattern. Speckle contrast (measured as
the standard deviation of fluorescence intensity along the microtubule
divided by the mean fluorescence intensity) decreased as the fraction
of labeled tubulin increased, and it was not altered by the binding of
purified brain microtubule-associated proteins. Computer simulation of microtubule assembly with labeled and unlabeled tubulin showed that the
speckle patterns can be explained solely by the stochastic nature of
tubulin dimer association with a growing end. Speckle patterns can
provide fiduciary marks in the microtubule lattice for motility studies
or can be used to determine the fraction of labeled tubulin
microinjected into living cells.
Biophys J, October 1998, p. 2059-2069, Vol. 75, No. 4
© 1998 by the Biophysical Society 0006-3495/98/10/2059/11 $2.00
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