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Biophys J, December 1999, p. 3341-3349, Vol. 77, No. 6
*Department of Physiology and Center for Biomedical Imaging Technology, University of Connecticut Health Center, Farmington, Connecticut 06030 USA, and #Division of Applied Physics, Hebrew University, Jerusalem, Israel
By adapting a laser scanning microscope with a titanium
sapphire femtosecond pulsed laser and transmission optics, we are able
to produce live cell images based on the nonlinear optical phenomenon
of second harmonic generation (SHG). Second harmonic imaging (SHIM) is
an ideal method for probing membranes of living cells because it offers
the high resolution of nonlinear optical microscopy with the potential
for near-total avoidance of photobleaching and phototoxicity. The
technique has been implemented on three cell lines labeled with
membrane-staining dyes that have large nonlinear optical coefficients.
The images can be obtained within physiologically relevant time scales.
Both achiral and chiral dyes were used to compare image formation for
the case of single- and double-leaflet staining, and it was found that
chirality plays a significant role in the mechanism of contrast
generation. It is also shown that SHIM is highly sensitive to membrane
potential, with a depolarization of 25 mV resulting in an approximately
twofold loss of signal intensity.
Biophys J, December 1999, p. 3341-3349, Vol. 77, No. 6
© 1999 by the Biophysical Society 0006-3495/99/12/3341/09 $2.00
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