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A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide

Genetically encoded temperature indicators (GETIs) allow for real-time measurement of subcellular temperature dynamics in live cells. However, GETIs have suffered from poor temperature sensitivity, which may not be sufficient to resolve small heat production from a biological process. Here, we devel...

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Autores principales: Vu, Cong Quang, Fukushima, Shun-ichi, Wazawa, Tetsuichi, Nagai, Takeharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363741/
https://www.ncbi.nlm.nih.gov/pubmed/34389773
http://dx.doi.org/10.1038/s41598-021-96049-5
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author Vu, Cong Quang
Fukushima, Shun-ichi
Wazawa, Tetsuichi
Nagai, Takeharu
author_facet Vu, Cong Quang
Fukushima, Shun-ichi
Wazawa, Tetsuichi
Nagai, Takeharu
author_sort Vu, Cong Quang
collection PubMed
description Genetically encoded temperature indicators (GETIs) allow for real-time measurement of subcellular temperature dynamics in live cells. However, GETIs have suffered from poor temperature sensitivity, which may not be sufficient to resolve small heat production from a biological process. Here, we develop a highly-sensitive GETI, denoted as ELP-TEMP, comprised of a temperature-responsive elastin-like polypeptide (ELP) fused with a cyan fluorescent protein (FP), mTurquoise2 (mT), and a yellow FP, mVenus (mV), as the donor and acceptor, respectively, of Förster resonance energy transfer (FRET). At elevated temperatures, the ELP moiety in ELP-TEMP undergoes a phase transition leading to an increase in the FRET efficiency. In HeLa cells, ELP-TEMP responded to the temperature from 33 to 40 °C with a maximum temperature sensitivity of 45.1 ± 8.1%/°C, which was the highest ever temperature sensitivity among hitherto-developed fluorescent nanothermometers. Although ELP-TEMP showed sensitivity not only to temperature but also to macromolecular crowding and self-concentration, we were able to correct the output of ELP-TEMP to achieve accurate temperature measurements at a subcellular resolution. We successfully applied ELP-TEMP to accurately measure temperature changes in cells induced by a local heat spot, even if the temperature difference was as small as < 1 °C, and to visualize heat production from stimulated Ca(2+) influx in live HeLa cells induced by a chemical stimulation. Furthermore, we investigated temperatures in the nucleus and cytoplasm of live HeLa cells and found that their temperatures were almost the same within the temperature resolution of our measurement. Our study would contribute to better understanding of cellular temperature dynamics, and ELP-TEMP would be a useful GETI for the investigation of cell thermobiology.
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spelling pubmed-83637412021-08-17 A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide Vu, Cong Quang Fukushima, Shun-ichi Wazawa, Tetsuichi Nagai, Takeharu Sci Rep Article Genetically encoded temperature indicators (GETIs) allow for real-time measurement of subcellular temperature dynamics in live cells. However, GETIs have suffered from poor temperature sensitivity, which may not be sufficient to resolve small heat production from a biological process. Here, we develop a highly-sensitive GETI, denoted as ELP-TEMP, comprised of a temperature-responsive elastin-like polypeptide (ELP) fused with a cyan fluorescent protein (FP), mTurquoise2 (mT), and a yellow FP, mVenus (mV), as the donor and acceptor, respectively, of Förster resonance energy transfer (FRET). At elevated temperatures, the ELP moiety in ELP-TEMP undergoes a phase transition leading to an increase in the FRET efficiency. In HeLa cells, ELP-TEMP responded to the temperature from 33 to 40 °C with a maximum temperature sensitivity of 45.1 ± 8.1%/°C, which was the highest ever temperature sensitivity among hitherto-developed fluorescent nanothermometers. Although ELP-TEMP showed sensitivity not only to temperature but also to macromolecular crowding and self-concentration, we were able to correct the output of ELP-TEMP to achieve accurate temperature measurements at a subcellular resolution. We successfully applied ELP-TEMP to accurately measure temperature changes in cells induced by a local heat spot, even if the temperature difference was as small as < 1 °C, and to visualize heat production from stimulated Ca(2+) influx in live HeLa cells induced by a chemical stimulation. Furthermore, we investigated temperatures in the nucleus and cytoplasm of live HeLa cells and found that their temperatures were almost the same within the temperature resolution of our measurement. Our study would contribute to better understanding of cellular temperature dynamics, and ELP-TEMP would be a useful GETI for the investigation of cell thermobiology. Nature Publishing Group UK 2021-08-13 /pmc/articles/PMC8363741/ /pubmed/34389773 http://dx.doi.org/10.1038/s41598-021-96049-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Vu, Cong Quang
Fukushima, Shun-ichi
Wazawa, Tetsuichi
Nagai, Takeharu
A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
title A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
title_full A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
title_fullStr A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
title_full_unstemmed A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
title_short A highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
title_sort highly-sensitive genetically encoded temperature indicator exploiting a temperature-responsive elastin-like polypeptide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363741/
https://www.ncbi.nlm.nih.gov/pubmed/34389773
http://dx.doi.org/10.1038/s41598-021-96049-5
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