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Biophys J, November 1999, p. 2837-2849, Vol. 77, No. 5
*Department of Physics and §Department of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853 and #Department of Physics, University of Maryland, Baltimore County, Baltimore, Maryland 21250 USA
Multiphoton fluorescence photobleaching recovery (MP-FPR)
is a technique for measuring the three-dimensional (3D) mobility of
fluorescent molecules with 3D spatial resolution of a few microns. A
brief, intense flash of mode-locked laser light pulses excites fluorescent molecules via multiphoton excitation in an ellipsoidal focal volume and photobleaches a fraction. Because multiphoton excitation of fluorophores is intrinsically confined to the
high-intensity focal volume of the illuminating beam, the bleached
region is restricted to a known, three-dimensionally defined volume.
Fluorescence in this focal volume is measured with multiphoton
excitation, using the attenuated laser beam to measure fluorescence
recovery as fresh unbleached dye diffuses in. The time course of the
fluorescence recovery signal after photobleaching can be analyzed to
determine the diffusion coefficient of the fluorescent species. The
mathematical formulas used to fit MP-FPR recovery curves and the
techniques needed to properly utilize them to acquire the diffusion
coefficients of fluorescently labeled molecules within cells are
presented here. MP-FPR is demonstrated on calcein in RBL-2H3 cells,
using an anomalous subdiffusion model, as well as in aqueous solutions of wild-type green fluorescent protein, yielding a diffusion
coefficient of 8.7 × 10
7
cm2s
1 in excellent agreement with the results
of other techniques.
Biophys J, November 1999, p. 2837-2849, Vol. 77, No. 5
© 1999 by the Biophysical Society 0006-3495/99/11/2837/13 $2.00
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