» Articles » PMID: 7014571

Cell-substrate Contacts Illuminated by Total Internal Reflection Fluorescence

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1981 Apr 1
PMID 7014571
Citations 232
Authors
Affiliations
Soon will be listed here.
Abstract

A technique for exciting fluorescence exclusively from regions of contact between cultured cells and the substrate is presented. The technique utilizes the evanescent wave of a totally internally reflecting laser beam to excite only those fluorescent molecules within one light wavelength or less of the substrate surface. Demonstrations of this technique are given for two types of cell cultures: rat primary myotubes with acetylcholine receptors labeled by fluorescent alpha-bungarotoxin and human skin fibroblasts labeled by a fluorescent lipid probe. Total internal reflection fluorescence examination of cells appears to have promising applications, including visualization of the membrane and underlying cytoplasmic structures at cell-substrate contacts, dramatic reduction of autofluorescence from debris and thick cells, mapping of membranes topography, and visualization of reversible bound fluorescent ligands at membrane receptors.

Citing Articles

Biphasic glucose-stimulated insulin secretion over decades: a journey from measurements and modeling to mechanistic insights.

Peng X, Wang K, Chen L Life Metab. 2025; 4(1):loae038.

PMID: 39872989 PMC: 11770817. DOI: 10.1093/lifemeta/loae038.


MINFLUX fluorescence nanoscopy in biological tissue.

Moosmayer T, Kiszka K, Westphal V, Pape J, Leutenegger M, Steffens H Proc Natl Acad Sci U S A. 2024; 121(52):e2422020121.

PMID: 39705311 PMC: 11670107. DOI: 10.1073/pnas.2422020121.


A novel mechanism of microbial attachment: The flagellar pump of .

Picou T, Luo H, Polackwich R, Gabilondo B, McAllister R, Gagnon D PNAS Nexus. 2024; 3(12):pgae545.

PMID: 39660061 PMC: 11631216. DOI: 10.1093/pnasnexus/pgae545.


Photonic lantern TIRF microscopy for highly efficient, uniform, artifact-free imaging.

Husain A, Yerolatsitis S, Amezcua Correa R, Han K Opt Express. 2024; 32(21):37046-37058.

PMID: 39573578 PMC: 11595348. DOI: 10.1364/OE.533269.


Measurement precision bounds on aberrated single-molecule emission patterns.

Fang L, Huang F Opt Express. 2024; 32(18):31431-31447.

PMID: 39573278 PMC: 11595290. DOI: 10.1364/OE.527267.


References
1.
Bereiter-Hahn J, Fox C, THORELL B . Quantitative reflection contrast microscopy of living cells. J Cell Biol. 1979; 82(3):767-79. PMC: 2110483. DOI: 10.1083/jcb.82.3.767. View

2.
Wehland J, Osborn M, Weber K . Cell-to-substratum contacts in living cells: a direct correlation between interference-reflexion and indirect-immunofluorescence microscopy using antibodies against actin and alpha-actinin. J Cell Sci. 1979; 37:257-73. DOI: 10.1242/jcs.37.1.257. View

3.
Axelrod D . Crosslinkage and visualization of acetylcholine receptors on myotubes with biotinylated alpha-bungarotoxin and fluorescent avidin. Proc Natl Acad Sci U S A. 1980; 77(8):4823-7. PMC: 349939. DOI: 10.1073/pnas.77.8.4823. View

4.
Thompson N, Burghardt T, Axelrod D . Measuring surface dynamics of biomolecules by total internal reflection fluorescence with photobleaching recovery or correlation spectroscopy. Biophys J. 1981; 33(3):435-54. PMC: 1327440. DOI: 10.1016/S0006-3495(81)84905-3. View

5.
Burghardt T, Axelrod D . Total internal reflection/fluorescence photobleaching recovery study of serum albumin adsorption dynamics. Biophys J. 1981; 33(3):455-67. PMC: 1327441. DOI: 10.1016/S0006-3495(81)84906-5. View