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A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms

Electron microscopy (EM) achieves the highest spatial resolution in protein localization, but specific protein EM labeling has lacked generally applicable genetically encoded tags for in situ visualization in cells and tissues. Here we introduce “miniSOG” (for mini Singlet Oxygen Generator), a fluor...

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Detalles Bibliográficos
Autores principales: Shu, Xiaokun, Lev-Ram, Varda, Deerinck, Thomas J., Qi, Yingchuan, Ramko, Ericka B., Davidson, Michael W., Jin, Yishi, Ellisman, Mark H., Tsien, Roger Y.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3071375/
https://www.ncbi.nlm.nih.gov/pubmed/21483721
http://dx.doi.org/10.1371/journal.pbio.1001041
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author Shu, Xiaokun
Lev-Ram, Varda
Deerinck, Thomas J.
Qi, Yingchuan
Ramko, Ericka B.
Davidson, Michael W.
Jin, Yishi
Ellisman, Mark H.
Tsien, Roger Y.
author_facet Shu, Xiaokun
Lev-Ram, Varda
Deerinck, Thomas J.
Qi, Yingchuan
Ramko, Ericka B.
Davidson, Michael W.
Jin, Yishi
Ellisman, Mark H.
Tsien, Roger Y.
author_sort Shu, Xiaokun
collection PubMed
description Electron microscopy (EM) achieves the highest spatial resolution in protein localization, but specific protein EM labeling has lacked generally applicable genetically encoded tags for in situ visualization in cells and tissues. Here we introduce “miniSOG” (for mini Singlet Oxygen Generator), a fluorescent flavoprotein engineered from Arabidopsis phototropin 2. MiniSOG contains 106 amino acids, less than half the size of Green Fluorescent Protein. Illumination of miniSOG generates sufficient singlet oxygen to locally catalyze the polymerization of diaminobenzidine into an osmiophilic reaction product resolvable by EM. MiniSOG fusions to many well-characterized proteins localize correctly in mammalian cells, intact nematodes, and rodents, enabling correlated fluorescence and EM from large volumes of tissue after strong aldehyde fixation, without the need for exogenous ligands, probes, or destructive permeabilizing detergents. MiniSOG permits high quality ultrastructural preservation and 3-dimensional protein localization via electron tomography or serial section block face scanning electron microscopy. EM shows that miniSOG-tagged SynCAM1 is presynaptic in cultured cortical neurons, whereas miniSOG-tagged SynCAM2 is postsynaptic in culture and in intact mice. Thus SynCAM1 and SynCAM2 could be heterophilic partners. MiniSOG may do for EM what Green Fluorescent Protein did for fluorescence microscopy.
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spelling pubmed-30713752011-04-11 A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms Shu, Xiaokun Lev-Ram, Varda Deerinck, Thomas J. Qi, Yingchuan Ramko, Ericka B. Davidson, Michael W. Jin, Yishi Ellisman, Mark H. Tsien, Roger Y. PLoS Biol Research Article Electron microscopy (EM) achieves the highest spatial resolution in protein localization, but specific protein EM labeling has lacked generally applicable genetically encoded tags for in situ visualization in cells and tissues. Here we introduce “miniSOG” (for mini Singlet Oxygen Generator), a fluorescent flavoprotein engineered from Arabidopsis phototropin 2. MiniSOG contains 106 amino acids, less than half the size of Green Fluorescent Protein. Illumination of miniSOG generates sufficient singlet oxygen to locally catalyze the polymerization of diaminobenzidine into an osmiophilic reaction product resolvable by EM. MiniSOG fusions to many well-characterized proteins localize correctly in mammalian cells, intact nematodes, and rodents, enabling correlated fluorescence and EM from large volumes of tissue after strong aldehyde fixation, without the need for exogenous ligands, probes, or destructive permeabilizing detergents. MiniSOG permits high quality ultrastructural preservation and 3-dimensional protein localization via electron tomography or serial section block face scanning electron microscopy. EM shows that miniSOG-tagged SynCAM1 is presynaptic in cultured cortical neurons, whereas miniSOG-tagged SynCAM2 is postsynaptic in culture and in intact mice. Thus SynCAM1 and SynCAM2 could be heterophilic partners. MiniSOG may do for EM what Green Fluorescent Protein did for fluorescence microscopy. Public Library of Science 2011-04-05 /pmc/articles/PMC3071375/ /pubmed/21483721 http://dx.doi.org/10.1371/journal.pbio.1001041 Text en Shu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shu, Xiaokun
Lev-Ram, Varda
Deerinck, Thomas J.
Qi, Yingchuan
Ramko, Ericka B.
Davidson, Michael W.
Jin, Yishi
Ellisman, Mark H.
Tsien, Roger Y.
A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms
title A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms
title_full A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms
title_fullStr A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms
title_full_unstemmed A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms
title_short A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms
title_sort genetically encoded tag for correlated light and electron microscopy of intact cells, tissues, and organisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3071375/
https://www.ncbi.nlm.nih.gov/pubmed/21483721
http://dx.doi.org/10.1371/journal.pbio.1001041
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