TY - JOUR
T1 - Photooxidation technology for correlated light and electron microscopy
AU - Meißlitzer-Ruppitsch, C.
AU - Röhrl, C.
AU - Neumüller, J.
AU - Pavelka, M.
AU - Ellinger, A.
PY - 2009/9
Y1 - 2009/9
N2 - The combination of the capabilities of light microscopical techniques with the power of resolution of electron microscopy along with technical advances has led to a gradual decline of the gap between classical light and electron microscopy. Among the correlative techniques using the synergistic opportunities, photooxidation methods have been established as valuable tools for visualizing cell structures at both light and electron microscopic level. Fluorescent dyes are used to oxidize the substrate diaminobenzidine, which in its oxidized state forms fine granular precipitates. Stained with osmium, the diaminobenzidine precipitates are well discernible in the electron microscope, thus labelling and defining the cellular structures, which at light microscopy level are recorded by fluorescent probes. The underlying photooxidation reaction is based on the excitation of free oxygen radicals that form upon illumination of fluorochromes; this is a central step in the procedure, which mainly influences the success of the method. This article summarizes basic steps of the technology and progresses, shows efforts and elaborated pathways, and focuses on methodical solutions as to the applicability of different fluorochromes, as well as conditions for fine structural localizations of the reaction products.
AB - The combination of the capabilities of light microscopical techniques with the power of resolution of electron microscopy along with technical advances has led to a gradual decline of the gap between classical light and electron microscopy. Among the correlative techniques using the synergistic opportunities, photooxidation methods have been established as valuable tools for visualizing cell structures at both light and electron microscopic level. Fluorescent dyes are used to oxidize the substrate diaminobenzidine, which in its oxidized state forms fine granular precipitates. Stained with osmium, the diaminobenzidine precipitates are well discernible in the electron microscope, thus labelling and defining the cellular structures, which at light microscopy level are recorded by fluorescent probes. The underlying photooxidation reaction is based on the excitation of free oxygen radicals that form upon illumination of fluorochromes; this is a central step in the procedure, which mainly influences the success of the method. This article summarizes basic steps of the technology and progresses, shows efforts and elaborated pathways, and focuses on methodical solutions as to the applicability of different fluorochromes, as well as conditions for fine structural localizations of the reaction products.
KW - 3D modelling
KW - BODIPY
KW - Correlative microscopy
KW - Fluorescent proteins
KW - Golgi apparatus
KW - Photooxidation
KW - Microscopy, Electron/methods
KW - Oxidation-Reduction
KW - Osmium/metabolism
KW - 3,3'-Diaminobenzidine/metabolism
KW - Microscopy/methods
KW - Fluorescent Dyes/metabolism
KW - Staining and Labeling/methods
UR - http://www.scopus.com/inward/record.url?scp=69249102102&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2818.2009.03220.x
DO - 10.1111/j.1365-2818.2009.03220.x
M3 - Review article
C2 - 19754726
AN - SCOPUS:69249102102
SN - 0022-2720
VL - 235
SP - 322
EP - 335
JO - Journal of Microscopy
JF - Journal of Microscopy
IS - 3
ER -