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Near‐field confocal optical spectroscopy (NCOS): subdiffraction optical resolution for biological systems
Author(s) -
HAYDON P. G.,
MARCHESE-RAGONA S.,
BASARSKY T. A.,
SZULCZEWSKI M.,
McCLOSKEY M.
Publication year - 1996
Publication title -
journal of microscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.569
H-Index - 111
eISSN - 1365-2818
pISSN - 0022-2720
DOI - 10.1111/j.1365-2818.1996.tb04798.x
Subject(s) - optics , resolution (logic) , microscopy , confocal microscopy , confocal , near field scanning optical microscope , materials science , optical microscope , light sheet fluorescence microscopy , microscope , image resolution , bright field microscopy , spectroscopy , near and far field , scanning confocal electron microscopy , physics , computer science , scanning electron microscope , quantum mechanics , artificial intelligence
Optical resolution is limited by diffraction. However. in near‐field microscopes sample illumination is provided through a subwavelength aperture to increase optical resolution. In this study we have evaluated the usefulness of this technique for living biological systems and report two significant improvements in this form of microscopy to enhance optical resolution for biological studies. We report a unique feedback method, photon‐density feedback, which is used to monitor the registration of a near‐field illumination probe with living cell membranes. In this method, the fluorescence intensity of a uniformly distributed fluorochrome is monitored while the sample is moved in the z‐axis towards the probe. Upon contact between the cell membrane and the near‐field probe a maximum intensity is detected. A problem with near‐field microscopy is that enhanced optical resolution is only achieved within the near‐field of the illuminating aperture. Thick biological specimens also fluoresce in the far‐field reducing optical resolution. To reduce this problem we incorporated a confocal pinhole together with the near‐field probe to enhance the resolution of this form of near‐field microscopy. Finally, we demonstrate that near‐field confocal optical spectroscopy does not impair physiological properties of neurons, astrocytes or mast cells, indicating that this high‐resolution optical methodology will permit a new approach to the study of molecular distribution and action within living specimens.