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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...

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Autores principales: Saito, Kenta, Hatsugai, Noriyuki, Horikawa, Kazuki, Kobayashi, Kentaro, Matsu-ura, Toru, Mikoshiba, Katsuhiko, Nagai, Takeharu
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
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.
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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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