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Biophys J, September 2000, p. 1655-1669, Vol. 79, No. 3
Department of Physics and Biophysics Research Division, University of Michigan, Ann Arbor, Michigan 48109 USA
Although reversible chemistry is crucial to dynamical
processes in living cells, relatively little is known about relevant chemical kinetic rates in vivo. Total internal reflection/fluorescence recovery after photobleaching (TIR/FRAP), an established technique previously demonstrated to measure reversible biomolecular kinetic rates at surfaces in vitro, is extended here to measure reversible biomolecular kinetic rates of actin at the cytofacial (subplasma membrane) surface of living cells. For the first time, spatial imaging
(with a charge-coupled device camera) is used in conjunction with
TIR/FRAP. TIR/FRAP imaging produces both spatial maps of kinetic
parameters (off-rates and mobile fractions) and estimates of kinetic
correlation distances, cell-wide kinetic gradients, and dependences of
kinetic parameters on initial fluorescence intensity. For microinjected
rhodamine actin in living cultured smooth muscle (BC3H1) cells, the
unbinding rate at or near the cytofacial surface of the plasma membrane
(averaged over the entire cell) is measured at 0.032 ± 0.007 s
1. The corresponding rate for actin marked by
microinjected rhodamine phalloidin is very similar, 0.033 ± 0.013 s
1, suggesting that TIR/FRAP is reporting the dynamics of
entire filaments or protofilaments. For submembrane fluorescence-marked actin, the intensity, off-rate, and mobile fraction show a positive correlation over a characteristic distance of 1-3 µm and a negative correlation over larger distances greater than ~7-14 µm.
Furthermore, the kinetic parameters display a statistically significant
cell-wide gradient, with the cell having a "fast" and "slow"
end with respect to actin kinetics.
Biophys J, September 2000, p. 1655-1669, Vol. 79, No. 3
© 2000 by the Biophysical Society 0006-3495/00/09/1655/15 $2.00
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