Author
Listed:
- Kenta Saito
(Institute of Scientific and Industrial Research, Osaka University
Research Institute for Electronic Science, Hokkaido University)
- Y-F Chang
(Institute of Scientific and Industrial Research, Osaka University)
- Kazuki Horikawa
(Centre for Frontier Research, National Institute of Genetics)
- Noriyuki Hatsugai
(Institute of Scientific and Industrial Research, Osaka University
Research Centre for Cooperative Projects, Hokkaido University)
- Yuriko Higuchi
(Graduate School of Pharmaceutical Sciences, Kyoto University
PRESTO, Japan Science and Technology Agency, Sanbancho, Chiyoda-ku)
- Mitsuru Hashida
(Graduate School of Pharmaceutical Sciences, Kyoto University)
- Yu Yoshida
(Research Institute for Electronic Science, Hokkaido University)
- Tomoki Matsuda
(Institute of Scientific and Industrial Research, Osaka University
Research Institute for Electronic Science, Hokkaido University)
- Yoshiyuki Arai
(Institute of Scientific and Industrial Research, Osaka University
Research Institute for Electronic Science, Hokkaido University)
- Takeharu Nagai
(Institute of Scientific and Industrial Research, Osaka University
Research Institute for Electronic Science, Hokkaido University
Research Centre for Cooperative Projects, Hokkaido University
PRESTO, Japan Science and Technology Agency, Sanbancho, Chiyoda-ku)
Abstract
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 Ca2+, 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.
Suggested Citation
Kenta Saito & Y-F Chang & Kazuki Horikawa & Noriyuki Hatsugai & Yuriko Higuchi & Mitsuru Hashida & Yu Yoshida & Tomoki Matsuda & Yoshiyuki Arai & Takeharu Nagai, 2012.
"Luminescent proteins for high-speed single-cell and whole-body imaging,"
Nature Communications, Nature, vol. 3(1), pages 1-9, January.
Handle:
RePEc:nat:natcom:v:3:y:2012:i:1:d:10.1038_ncomms2248
DOI: 10.1038/ncomms2248
Download full text from publisher
Citations
Citations are extracted by the
CitEc Project, subscribe to its
RSS feed for this item.
Cited by:
- Assunta Merolla & Caterina Michetti & Matteo Moschetta & Francesca Vacca & Lorenzo Ciano & Laura Emionite & Simonetta Astigiano & Alessandra Romei & Simone Horenkamp & Ken Berglund & Robert E. Gross &, 2024.
"A pH-sensitive closed-loop nanomachine to control hyperexcitability at the single neuron level,"
Nature Communications, Nature, vol. 15(1), pages 1-21, December.
- Xiaodong Tian & Yiyu Zhang & Xinyu Li & Ying Xiong & Tianchen Wu & Hui-Wang Ai, 2022.
"A luciferase prosubstrate and a red bioluminescent calcium indicator for imaging neuronal activity in mice,"
Nature Communications, Nature, vol. 13(1), pages 1-13, December.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:3:y:2012:i:1:d:10.1038_ncomms2248. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.