Literature DB >> 2211864

Total internal reflection fluorescence (TIRF) microscopy. I. Modelling cell contact region fluorescence.

W M Reichert1, G A Truskey.   

Abstract

Total Internal Reflection Fluorescence (TIRF) is a powerful technique for visualizing focal and close contacts between the cell and the surface. Practical application of TIRF has been hampered by the lack of straightforward methods to calculate separation distances. The characteristic matrix theory of thin dielectric films was used to develop simple exponential approximations for the fluorescence excited in the cell-substratum contact region during a TIRF experiment. Two types of fluorescence were examined: fluorescently labeled cell membranes, and a fluorescent water-soluble dye. By neglecting the refractive index of the cell membrane, the fluorescence excited in the cell membrane was modelled by a single exponential function while the fluorescence in the membrane/substratum water gap followed a weighted sum of two exponentials. The error associated with neglecting the cell membrane for an incident angle of 70 degrees never exceeded 2.5%, regardless of the cell-substratum separation distance. Comparisons of approximated fluorescence intensities to more exact solutions of the fluorescence integrals for the three-phase model indicated that the approximations are accurate to about 1% for membrane/substratum gap thicknesses of less than 50 nm if the cytoplasmic and water gap refractive indices are known. The intrinsic error of this model in the determination of membrane/substratum separations was 10% as long as the uncertainties in the water gap and cytoplasmic refractive indices were less than 1%.

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Year:  1990        PMID: 2211864     DOI: 10.1242/jcs.96.2.219

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  25 in total

1.  Atomic force and total internal reflection fluorescence microscopy for the study of force transmission in endothelial cells.

Authors:  A B Mathur; G A Truskey; W M Reichert
Journal:  Biophys J       Date:  2000-04       Impact factor: 4.033

2.  Observing secretory granules with a multiangle evanescent wave microscope.

Authors:  A Rohrbach
Journal:  Biophys J       Date:  2000-05       Impact factor: 4.033

Review 3.  Evanescent-wave microscopy: a new tool to gain insight into the control of transmitter release.

Authors:  M Oheim; D Loerke; R H Chow; W Stühmer
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-02-28       Impact factor: 6.237

4.  Combined light microscopy and attenuated total reflection fourier transform infrared spectroscopy for integration of biofilm structure, distribution, and chemistry at solid-liquid interfaces.

Authors:  P A Suci; K J Siedlecki; R J Palmer; D C White; G G Geesey
Journal:  Appl Environ Microbiol       Date:  1997-11       Impact factor: 4.792

5.  Three-dimensional total-internal reflection fluorescence nanoscopy with nanometric axial resolution by photometric localization of single molecules.

Authors:  Alan M Szalai; Bruno Siarry; Jerónimo Lukin; David J Williamson; Nicolás Unsain; Alfredo Cáceres; Mauricio Pilo-Pais; Guillermo Acuna; Damián Refojo; Dylan M Owen; Sabrina Simoncelli; Fernando D Stefani
Journal:  Nat Commun       Date:  2021-01-22       Impact factor: 14.919

6.  Molecular accessibility in relation to cell surface topography and compression against a flat substrate.

Authors:  Sandrine A Hocdé; Ollivier Hyrien; Richard E Waugh
Journal:  Biophys J       Date:  2009-07-08       Impact factor: 4.033

7.  Mapping fluorophore distributions in three dimensions by quantitative multiple angle-total internal reflection fluorescence microscopy.

Authors:  B P Olveczky; N Periasamy; A S Verkman
Journal:  Biophys J       Date:  1997-11       Impact factor: 4.033

8.  Enhanced live cell imaging via photonic crystal enhanced fluorescence microscopy.

Authors:  Weili Chen; Kenneth D Long; Hojeong Yu; Yafang Tan; Ji Sun Choi; Brendan A Harley; Brian T Cunningham
Journal:  Analyst       Date:  2014-11-21       Impact factor: 4.616

9.  Cell volume measured by total internal reflection microfluorimetry: application to water and solute transport in cells transfected with water channel homologs.

Authors:  J Farinas; V Simanek; A S Verkman
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

10.  Cytoplasmic viscosity near the cell plasma membrane: translational diffusion of a small fluorescent solute measured by total internal reflection-fluorescence photobleaching recovery.

Authors:  R Swaminathan; S Bicknese; N Periasamy; A S Verkman
Journal:  Biophys J       Date:  1996-08       Impact factor: 4.033

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