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A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo
Orange-red fluorescent proteins (FPs) are widely used in biomedical research for multiplexed epifluorescence microscopy with GFP-based probes, but their different excitation requirements make multiplexing with new advanced microscopy methods difficult. Separately, orange-red FPs are useful for deep-...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942401/ https://www.ncbi.nlm.nih.gov/pubmed/27240196 http://dx.doi.org/10.1038/nbt.3550 |
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author | Chu, Jun Oh, Young-Hee Sens, Alex Ataie, Niloufar Dana, Hod Macklin, John J. Laviv, Tal Welf, Erik S. Dean, Kevin M. Zhang, Feijie Kim, Benjamin B. Tang, Clement Tran Hu, Michelle Baird, Michelle A. Davidson, Michael W. Kay, Mark A. Fiolka, Reto Yasuda, Ryohei Kim, Douglas S. Ng, Ho-Leung Lin, Michael Z. |
author_facet | Chu, Jun Oh, Young-Hee Sens, Alex Ataie, Niloufar Dana, Hod Macklin, John J. Laviv, Tal Welf, Erik S. Dean, Kevin M. Zhang, Feijie Kim, Benjamin B. Tang, Clement Tran Hu, Michelle Baird, Michelle A. Davidson, Michael W. Kay, Mark A. Fiolka, Reto Yasuda, Ryohei Kim, Douglas S. Ng, Ho-Leung Lin, Michael Z. |
author_sort | Chu, Jun |
collection | PubMed |
description | Orange-red fluorescent proteins (FPs) are widely used in biomedical research for multiplexed epifluorescence microscopy with GFP-based probes, but their different excitation requirements make multiplexing with new advanced microscopy methods difficult. Separately, orange-red FPs are useful for deep-tissue imaging in mammals due to the relative tissue transmissibility of orange-red light, but their dependence on illumination limits their sensitivity as reporters in deep tissues. Here we describe CyOFP1, a bright engineered orange-red FP that is excitable by cyan light. We show that CyOFP1 enables single-excitation multiplexed imaging with GFP-based probes in single-photon and two-photon microscopy, including time-lapse imaging in light-sheet systems. CyOFP1 also serves as an efficient acceptor for resonance energy transfer from the highly catalytic blue-emitting luciferase NanoLuc. An optimized fusion of CyOFP1 and NanoLuc, called Antares, functions as a highly sensitive bioluminescent reporter in vivo, producing substantially brighter signals from deep tissues than firefly luciferase and other bioluminescent proteins. |
format | Online Article Text |
id | pubmed-4942401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-49424012016-11-30 A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo Chu, Jun Oh, Young-Hee Sens, Alex Ataie, Niloufar Dana, Hod Macklin, John J. Laviv, Tal Welf, Erik S. Dean, Kevin M. Zhang, Feijie Kim, Benjamin B. Tang, Clement Tran Hu, Michelle Baird, Michelle A. Davidson, Michael W. Kay, Mark A. Fiolka, Reto Yasuda, Ryohei Kim, Douglas S. Ng, Ho-Leung Lin, Michael Z. Nat Biotechnol Article Orange-red fluorescent proteins (FPs) are widely used in biomedical research for multiplexed epifluorescence microscopy with GFP-based probes, but their different excitation requirements make multiplexing with new advanced microscopy methods difficult. Separately, orange-red FPs are useful for deep-tissue imaging in mammals due to the relative tissue transmissibility of orange-red light, but their dependence on illumination limits their sensitivity as reporters in deep tissues. Here we describe CyOFP1, a bright engineered orange-red FP that is excitable by cyan light. We show that CyOFP1 enables single-excitation multiplexed imaging with GFP-based probes in single-photon and two-photon microscopy, including time-lapse imaging in light-sheet systems. CyOFP1 also serves as an efficient acceptor for resonance energy transfer from the highly catalytic blue-emitting luciferase NanoLuc. An optimized fusion of CyOFP1 and NanoLuc, called Antares, functions as a highly sensitive bioluminescent reporter in vivo, producing substantially brighter signals from deep tissues than firefly luciferase and other bioluminescent proteins. 2016-05-30 2016-07 /pmc/articles/PMC4942401/ /pubmed/27240196 http://dx.doi.org/10.1038/nbt.3550 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Chu, Jun Oh, Young-Hee Sens, Alex Ataie, Niloufar Dana, Hod Macklin, John J. Laviv, Tal Welf, Erik S. Dean, Kevin M. Zhang, Feijie Kim, Benjamin B. Tang, Clement Tran Hu, Michelle Baird, Michelle A. Davidson, Michael W. Kay, Mark A. Fiolka, Reto Yasuda, Ryohei Kim, Douglas S. Ng, Ho-Leung Lin, Michael Z. A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
title | A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
title_full | A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
title_fullStr | A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
title_full_unstemmed | A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
title_short | A bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
title_sort | bright cyan-excitable orange fluorescent protein facilitates dual-emission microscopy and enhances bioluminescence imaging in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942401/ https://www.ncbi.nlm.nih.gov/pubmed/27240196 http://dx.doi.org/10.1038/nbt.3550 |
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