Title of article
4Pi-confocal microscopy of live cells
Author/Authors
Bahlmann، نويسنده , , Karsten and Jakobs، نويسنده , , Stefan and Hell، نويسنده , , Stefan W.، نويسنده ,
Issue Information
دوماهنامه با شماره پیاپی سال 2001
Pages
10
From page
155
To page
164
Abstract
By coherently adding the spherical wavefronts of two opposing lenses, two-photon excitation 4Pi-confocal fluorescence microscopy has achieved three-dimensional imaging with an axial resolution 3–7 times better than confocal microscopy. So far this improvement was possible only in glycerol-mounted, fixed cells. Here we report 4Pi-confocal microscopy of watery objects and its application to the imaging of live cells. Water immersion of 4Pi-confocal microscopy of membrane stained live Escherichia coli bacteria attains a 4.3-fold better axial resolution as compared to the best water immersion confocal microscope. The resolution enhancement results into a vastly improved three-dimensional representation of the bacteria. The first images of live biological samples with an all-directional resolution in the 190–280 nm range are presented here, thus establishing a new resolution benchmark in live-cell microscopy.
Keywords
RESOLUTION , confocal , E. coli , 4pi
Journal title
Ultramicroscopy
Serial Year
2001
Journal title
Ultramicroscopy
Record number
2155630
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