학술논문

Fluorescence photooxidation with eosin: a method for high resolution immunolocalization and in situ hybridization detection for light and electron microscopy.
Document Type
article
Source
Journal of Cell Biology. 126(4)
Subject
Biochemistry and Cell Biology
Biological Sciences
Animals
Aorta
Bacterial Proteins
Calsequestrin
Cattle
Cells
Cultured
Endothelium
Vascular
Eosine Yellowish-(YS)
Immunohistochemistry
In Situ Hybridization
Indicators and Reagents
Microscopy
Fluorescence
Microscopy
Immunoelectron
Oxidation-Reduction
Photochemistry
Streptavidin
Tubulin
Medical and Health Sciences
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Language
Abstract
A simple method is described for high-resolution light and electron microscopic immunolocalization of proteins in cells and tissues by immunofluorescence and subsequent photooxidation of diaminobenzidine tetrahydrochloride into an insoluble osmiophilic polymer. By using eosin as the fluorescent marker, a substantial improvement in sensitivity is achieved in the photooxidation process over other conventional fluorescent compounds. The technique allows for precise correlative immunolocalization studies on the same sample using fluorescence, transmitted light and electron microscopy. Furthermore, because eosin is smaller in size than other conventional markers, this method results in improved penetration of labeling reagents compared to gold or enzyme based procedures. The improved penetration allows for three-dimensional immunolocalization using high voltage electron microscopy. Fluorescence photooxidation can also be used for high resolution light and electron microscopic localization of specific nucleic acid sequences by in situ hybridization utilizing biotinylated probes followed by an eosin-streptavidin conjugate.