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Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level
BACKGROUND: Efficient bioluminescence resonance energy transfer (BRET) from a bioluminescent protein to a fluorescent protein with high fluorescent quantum yield has been utilized to enhance luminescence intensity, allowing single-cell imaging in near real time without external light illumination. M...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848576/ https://www.ncbi.nlm.nih.gov/pubmed/20376337 http://dx.doi.org/10.1371/journal.pone.0009935 |
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author | Saito, Kenta Hatsugai, Noriyuki Horikawa, Kazuki Kobayashi, Kentaro Matsu-ura, Toru Mikoshiba, Katsuhiko Nagai, Takeharu |
author_facet | Saito, Kenta Hatsugai, Noriyuki Horikawa, Kazuki Kobayashi, Kentaro Matsu-ura, Toru Mikoshiba, Katsuhiko Nagai, Takeharu |
author_sort | Saito, Kenta |
collection | PubMed |
description | BACKGROUND: Efficient bioluminescence resonance energy transfer (BRET) from a bioluminescent protein to a fluorescent protein with high fluorescent quantum yield has been utilized to enhance luminescence intensity, allowing single-cell imaging in near real time without external light illumination. METHODOLOGY/PRINCIPAL FINDINGS: We applied BRET to develop an autoluminescent Ca(2+) indicator, BRAC, which is composed of Ca(2+)-binding protein, calmodulin, and its target peptide, M13, sandwiched between a yellow fluorescent protein variant, Venus, and an enhanced Renilla luciferase, RLuc8. Adjusting the relative dipole orientation of the luminescent protein's chromophores improved the dynamic range of BRET signal change in BRAC up to 60%, which is the largest dynamic range among BRET-based indicators reported so far. Using BRAC, we demonstrated successful visualization of Ca(2+) dynamics at the single-cell level with temporal resolution at 1 Hz. Moreover, BRAC signals were acquired by ratiometric imaging capable of canceling out Ca(2+)-independent signal drifts due to change in cell shape, focus shift, etc. CONCLUSIONS/SIGNIFICANCE: The brightness and large dynamic range of BRAC should facilitate high-sensitive Ca(2+) imaging not only in single live cells but also in small living subjects. |
format | Text |
id | pubmed-2848576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28485762010-04-07 Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level Saito, Kenta Hatsugai, Noriyuki Horikawa, Kazuki Kobayashi, Kentaro Matsu-ura, Toru Mikoshiba, Katsuhiko Nagai, Takeharu PLoS One Research Article BACKGROUND: Efficient bioluminescence resonance energy transfer (BRET) from a bioluminescent protein to a fluorescent protein with high fluorescent quantum yield has been utilized to enhance luminescence intensity, allowing single-cell imaging in near real time without external light illumination. METHODOLOGY/PRINCIPAL FINDINGS: We applied BRET to develop an autoluminescent Ca(2+) indicator, BRAC, which is composed of Ca(2+)-binding protein, calmodulin, and its target peptide, M13, sandwiched between a yellow fluorescent protein variant, Venus, and an enhanced Renilla luciferase, RLuc8. Adjusting the relative dipole orientation of the luminescent protein's chromophores improved the dynamic range of BRET signal change in BRAC up to 60%, which is the largest dynamic range among BRET-based indicators reported so far. Using BRAC, we demonstrated successful visualization of Ca(2+) dynamics at the single-cell level with temporal resolution at 1 Hz. Moreover, BRAC signals were acquired by ratiometric imaging capable of canceling out Ca(2+)-independent signal drifts due to change in cell shape, focus shift, etc. CONCLUSIONS/SIGNIFICANCE: The brightness and large dynamic range of BRAC should facilitate high-sensitive Ca(2+) imaging not only in single live cells but also in small living subjects. Public Library of Science 2010-04-01 /pmc/articles/PMC2848576/ /pubmed/20376337 http://dx.doi.org/10.1371/journal.pone.0009935 Text en Saito 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 Saito, Kenta Hatsugai, Noriyuki Horikawa, Kazuki Kobayashi, Kentaro Matsu-ura, Toru Mikoshiba, Katsuhiko Nagai, Takeharu Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level |
title | Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level |
title_full | Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level |
title_fullStr | Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level |
title_full_unstemmed | Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level |
title_short | Auto-Luminescent Genetically-Encoded Ratiometric Indicator for Real-Time Ca(2+) Imaging at the Single Cell Level |
title_sort | auto-luminescent genetically-encoded ratiometric indicator for real-time ca(2+) imaging at the single cell level |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848576/ https://www.ncbi.nlm.nih.gov/pubmed/20376337 http://dx.doi.org/10.1371/journal.pone.0009935 |
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