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PMID: 6827590 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Total internal inflection fluorescent microscopy.

Journal of microscopy ·Vol. 129 ·No. Pt 1 ·1983-01-00 ·Pages 19-28

Axelrod D, Thompson NL, Burghardt TP

Abstract

This review discusses applications of fluorescence microscopy using totally internally reflected excitation light. When totally internally reflected in a transparent solid at its interface liquid, the excitation light beam penetrates only a short distance into the liquid. This surface electromagnetic field, called the 'evanescent wave', can selectively excite fluorescent molecules in the liquid near the interface. Total internal reflection fluorescence (TIRF) has been used to examine the cell/substrate contact regions of primary cultured rat myotubes with acetylcholine receptors labelled by fluorescent alpha-bungarotoxin and human skin fibroblasts labelled with a membrane-incorporated fluorescent lipid. TIRF examination of cell/surface contacts dramatically reduces background from cell autofluorescence and debris. TIRF has also been combined with fluorescence photobleaching recovery and correlation spectroscopy to measure the chemical kinetic binding rates and surface diffusion constant of fluorescent labelled serum protein binding (at equilibrium) to a surface.

MeSH Terms
Animals Cells, Cultured Fibroblasts Fluorescent Dyes Humans Lipid Bilayers/analysis Microscopy, Fluorescence Muscles Rats Receptors, Cholinergic/analysis
Chemicals
Fluorescent Dyes Lipid Bilayers Receptors, Cholinergic
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Axelrod D
Thompson N L
Burghardt T P
Article Info
Journal
Journal of microscopy
Abbr.
J Microsc
ISSN
0022-2720
Published
1983-01-00
Pages
19-28
Language
English
Region
England
NLM ID
0204522
Subset
IM
Grants
NHLBI NIH HHS · 1RO1-HL 24039 · United States
NINDS NIH HHS · 2RO1-NS 14565 · United States
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