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Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo
Selective targeting of DNA by means of fluorescent labeling has become a mainstay in the life sciences. While genetic engineering serves as a powerful technique and allows the visualization of nucleic acid by using DNA‐targeting fluorescent fusion proteins in a cell‐type‐ and subcellular‐specific ma...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894298/ https://www.ncbi.nlm.nih.gov/pubmed/32974998 http://dx.doi.org/10.1002/cbic.202000465 |
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author | Lämmle, Carina A. Varady, Adam Müller, Thorsten G. Sturtzel, Caterina Riepl, Michael Mathes, Bettina Eichhorst, Jenny Sporbert, Anje Lehmann, Martin Kräusslich, Hans‐Georg Distel, Martin Broichhagen, Johannes |
author_facet | Lämmle, Carina A. Varady, Adam Müller, Thorsten G. Sturtzel, Caterina Riepl, Michael Mathes, Bettina Eichhorst, Jenny Sporbert, Anje Lehmann, Martin Kräusslich, Hans‐Georg Distel, Martin Broichhagen, Johannes |
author_sort | Lämmle, Carina A. |
collection | PubMed |
description | Selective targeting of DNA by means of fluorescent labeling has become a mainstay in the life sciences. While genetic engineering serves as a powerful technique and allows the visualization of nucleic acid by using DNA‐targeting fluorescent fusion proteins in a cell‐type‐ and subcellular‐specific manner, it relies on the introduction of foreign genes. On the other hand, DNA‐binding small fluorescent molecules can be used without genetic engineering, but they are not spatially restricted. Herein, we report a photocaged version of the DNA dye Hoechst33342 (pcHoechst), which can be uncaged by using UV to blue light for the selective staining of chromosomal DNA in subnuclear regions of live cells. Expanding its application to a vertebrate model organism, we demonstrate uncaging in epithelial cells and short‐term cell tracking in vivo in zebrafish. We envision pcHoechst as a valuable tool for targeting and interrogating DNA with precise spatiotemporal resolution in living cells and wild‐type organisms. |
format | Online Article Text |
id | pubmed-7894298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78942982021-03-02 Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo Lämmle, Carina A. Varady, Adam Müller, Thorsten G. Sturtzel, Caterina Riepl, Michael Mathes, Bettina Eichhorst, Jenny Sporbert, Anje Lehmann, Martin Kräusslich, Hans‐Georg Distel, Martin Broichhagen, Johannes Chembiochem Full Papers Selective targeting of DNA by means of fluorescent labeling has become a mainstay in the life sciences. While genetic engineering serves as a powerful technique and allows the visualization of nucleic acid by using DNA‐targeting fluorescent fusion proteins in a cell‐type‐ and subcellular‐specific manner, it relies on the introduction of foreign genes. On the other hand, DNA‐binding small fluorescent molecules can be used without genetic engineering, but they are not spatially restricted. Herein, we report a photocaged version of the DNA dye Hoechst33342 (pcHoechst), which can be uncaged by using UV to blue light for the selective staining of chromosomal DNA in subnuclear regions of live cells. Expanding its application to a vertebrate model organism, we demonstrate uncaging in epithelial cells and short‐term cell tracking in vivo in zebrafish. We envision pcHoechst as a valuable tool for targeting and interrogating DNA with precise spatiotemporal resolution in living cells and wild‐type organisms. John Wiley and Sons Inc. 2020-11-02 2021-02-02 /pmc/articles/PMC7894298/ /pubmed/32974998 http://dx.doi.org/10.1002/cbic.202000465 Text en © 2020 The Authors. ChemBioChem published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Lämmle, Carina A. Varady, Adam Müller, Thorsten G. Sturtzel, Caterina Riepl, Michael Mathes, Bettina Eichhorst, Jenny Sporbert, Anje Lehmann, Martin Kräusslich, Hans‐Georg Distel, Martin Broichhagen, Johannes Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo |
title | Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo
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title_full | Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo
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title_fullStr | Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo
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title_full_unstemmed | Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo
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title_short | Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo
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title_sort | photocaged hoechst enables subnuclear visualization and cell selective staining of dna in vivo |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894298/ https://www.ncbi.nlm.nih.gov/pubmed/32974998 http://dx.doi.org/10.1002/cbic.202000465 |
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