spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gingell, D.
Right arrow Articles by Mellor, J. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gingell, D.
Right arrow Articles by Mellor, J. S.

Journal of Cell Science, Vol 87, Issue 5 677-693, Copyright © 1987 by Company of Biologists


JOURNAL ARTICLES

General electromagnetic theory of total internal reflection fluorescence: the quantitative basis for mapping cell-substratum topography

D Gingell, OS Heavens and JS Mellor
Department of Anatomy and Biology, Middlesex Hospital Medical School, London, UK.

Total internal reflection fluorescence (TIRF) has recently been used to look at the contacts made between cells and a glass surface on which they are spread. Our method utilizes the fluorescence of a water-soluble dye that acts as an extracellular aqueous volume marker. Fluorescence is stimulated by the short-range electric field near the glass surface that exists under conditions of total internal reflection. Since fluorescence is normally generated beneath a spread cell and not beyond it, the fluorescence of the image is related to the size of the cell-glass water gap. The images obtained are remarkable for their detail, contrast and the absence of confusing granularity due to cytoplasmic heterogeneity, which is commonly seen in interference reflection (IRM) images. We here develop a rigorous electromagnetic theory of total internal reflection in layered structures appropriate for cell contacts and apply it to quantitative TIRF. We show that: (1) TIRF, unlike IRM, can report cell-glass gaps in a way that is practically independent of the detailed physical properties of the cell; (2) TIRF is also far more sensitive than IRM for measuring cell-glass water gaps up to approximately equal to 100nm. These striking results explain the image quality seen by TIRF. As the initial step towards verifying our theory we show that measurement of the fluorescence stimulated by total internal reflection at a simple glass-water interface matches theoretical predictions.


This article has been cited by other articles:


Home page
Appl. Environ. Microbiol.Home page
M. A.-S. Vigeant, R. M. Ford, M. Wagner, and L. K. Tamm
Reversible and Irreversible Adhesion of Motile Escherichia coli Cells Analyzed by Total Internal Reflection Aqueous Fluorescence Microscopy
Appl. Envir. Microbiol., June 1, 2002; 68(6): 2794 - 2801.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
G. A. Truskey, J. S. Burmeister, E. Grapa, and W. M. Reichert
Total internal reflection fluorescence microscopy (TIRFM). II. Topographical mapping of relative cell/substratum separation distances
J. Cell Sci., October 1, 1992; 103(2): 491 - 499.
[Abstract] [PDF]




© The Company of Biologists Ltd 1987