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Luminescent proteins for high-speed single-cell and whole-body imaging
The use of fluorescent proteins has revolutionized our understanding of biological processes. However, the requirement for external illumination precludes their universal application to the study of biological processes in all tissues. Although light can be created by chemiluminescence, light emissi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535334/ https://www.ncbi.nlm.nih.gov/pubmed/23232392 http://dx.doi.org/10.1038/ncomms2248 |
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author | Saito, Kenta Chang, Y-F Horikawa, Kazuki Hatsugai, Noriyuki Higuchi, Yuriko Hashida, Mitsuru Yoshida, Yu Matsuda, Tomoki Arai, Yoshiyuki Nagai, Takeharu |
author_facet | Saito, Kenta Chang, Y-F Horikawa, Kazuki Hatsugai, Noriyuki Higuchi, Yuriko Hashida, Mitsuru Yoshida, Yu Matsuda, Tomoki Arai, Yoshiyuki Nagai, Takeharu |
author_sort | Saito, Kenta |
collection | PubMed |
description | The use of fluorescent proteins has revolutionized our understanding of biological processes. However, the requirement for external illumination precludes their universal application to the study of biological processes in all tissues. Although light can be created by chemiluminescence, light emission from existing chemiluminescent probes is too weak to use this imaging modality in situations when fluorescence cannot be used. Here we report the development of the brightest luminescent protein to date, Nano-lantern, which is a chimera of enhanced Renilla luciferase and Venus, a fluorescent protein with high bioluminescence resonance energy transfer efficiency. Nano-lantern allows real-time imaging of intracellular structures in living cells with spatial resolution equivalent to fluorescence and sensitive tumour detection in freely moving unshaved mice. We also create functional indicators based on Nano-lantern that can image Ca(2+), cyclic adenosine monophosphate and adenosine 5′-triphosphate dynamics in environments where the use of fluorescent indicators is not feasible. These luminescent proteins allow visualization of biological phenomena at previously unseen single-cell, organ and whole-body level in animals and plants. |
format | Online Article Text |
id | pubmed-3535334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-35353342013-01-03 Luminescent proteins for high-speed single-cell and whole-body imaging Saito, Kenta Chang, Y-F Horikawa, Kazuki Hatsugai, Noriyuki Higuchi, Yuriko Hashida, Mitsuru Yoshida, Yu Matsuda, Tomoki Arai, Yoshiyuki Nagai, Takeharu Nat Commun Article The use of fluorescent proteins has revolutionized our understanding of biological processes. However, the requirement for external illumination precludes their universal application to the study of biological processes in all tissues. Although light can be created by chemiluminescence, light emission from existing chemiluminescent probes is too weak to use this imaging modality in situations when fluorescence cannot be used. Here we report the development of the brightest luminescent protein to date, Nano-lantern, which is a chimera of enhanced Renilla luciferase and Venus, a fluorescent protein with high bioluminescence resonance energy transfer efficiency. Nano-lantern allows real-time imaging of intracellular structures in living cells with spatial resolution equivalent to fluorescence and sensitive tumour detection in freely moving unshaved mice. We also create functional indicators based on Nano-lantern that can image Ca(2+), cyclic adenosine monophosphate and adenosine 5′-triphosphate dynamics in environments where the use of fluorescent indicators is not feasible. These luminescent proteins allow visualization of biological phenomena at previously unseen single-cell, organ and whole-body level in animals and plants. Nature Pub. Group 2012-12-11 /pmc/articles/PMC3535334/ /pubmed/23232392 http://dx.doi.org/10.1038/ncomms2248 Text en Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Saito, Kenta Chang, Y-F Horikawa, Kazuki Hatsugai, Noriyuki Higuchi, Yuriko Hashida, Mitsuru Yoshida, Yu Matsuda, Tomoki Arai, Yoshiyuki Nagai, Takeharu Luminescent proteins for high-speed single-cell and whole-body imaging |
title | Luminescent proteins for high-speed single-cell and whole-body imaging |
title_full | Luminescent proteins for high-speed single-cell and whole-body imaging |
title_fullStr | Luminescent proteins for high-speed single-cell and whole-body imaging |
title_full_unstemmed | Luminescent proteins for high-speed single-cell and whole-body imaging |
title_short | Luminescent proteins for high-speed single-cell and whole-body imaging |
title_sort | luminescent proteins for high-speed single-cell and whole-body imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535334/ https://www.ncbi.nlm.nih.gov/pubmed/23232392 http://dx.doi.org/10.1038/ncomms2248 |
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