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Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe

Extracellular ATP as a purinergic signaling molecule, together with ATP receptor, are playing an important role in tumor growth, therapy resistance, and host immunity suppression. Meanwhile ATP is a crucial indicator for cellular energy status and viability, thus a vital variable for tissue regenera...

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Autores principales: Liu, Wenjun, Zhu, Xuena, Mozneb, Maedeh, Nagahara, Larry, Hu, Tony Y., Li, Chen-Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459148/
https://www.ncbi.nlm.nih.gov/pubmed/34554325
http://dx.doi.org/10.1007/s00604-021-05012-8
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author Liu, Wenjun
Zhu, Xuena
Mozneb, Maedeh
Nagahara, Larry
Hu, Tony Y.
Li, Chen-Zhong
author_facet Liu, Wenjun
Zhu, Xuena
Mozneb, Maedeh
Nagahara, Larry
Hu, Tony Y.
Li, Chen-Zhong
author_sort Liu, Wenjun
collection PubMed
description Extracellular ATP as a purinergic signaling molecule, together with ATP receptor, are playing an important role in tumor growth, therapy resistance, and host immunity suppression. Meanwhile ATP is a crucial indicator for cellular energy status and viability, thus a vital variable for tissue regeneration and in vitro tissue engineering. Most recent studies on COVID-19 virus suggest infection caused ATP deficit and release as a major characterization at the early stage of the disease and major causes for disease complications. Thus, imaging ATP molecule in both cellular and extracellular contexts has many applications in biology, engineering, and clinics. A sensitive and selective fluorescence “signal-on” probe for ATP detection was constructed, based on the base recognition between a black hole quencher (BHQ)-labeled aptamer oligonucleotide and a fluorophore (Cy5)-labeled reporter flare. The probe was able to detect ATP in solution with single digit µM detection limit. With the assistance of lipofectamine, this probe efficiently entered and shined in the model cells U2OS within 3 h. Further application of the probe in specific scenery, cardio-tissue engineering, was also tested where the ATP aptamer complex was able to sense cellular ATP status in a semi-quantitative manner, representing a novel approach for selection of functional cardiomyocytes for tissue engineering. At last a slight change in probe configuration in which a flexible intermolecular A14 linker was introduced granted regeneration capability. These data support the application of this probe in multiple circumstances where ATP measurement or imaging is on demand. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-021-05012-8.
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spelling pubmed-84591482021-09-23 Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe Liu, Wenjun Zhu, Xuena Mozneb, Maedeh Nagahara, Larry Hu, Tony Y. Li, Chen-Zhong Mikrochim Acta Original Paper Extracellular ATP as a purinergic signaling molecule, together with ATP receptor, are playing an important role in tumor growth, therapy resistance, and host immunity suppression. Meanwhile ATP is a crucial indicator for cellular energy status and viability, thus a vital variable for tissue regeneration and in vitro tissue engineering. Most recent studies on COVID-19 virus suggest infection caused ATP deficit and release as a major characterization at the early stage of the disease and major causes for disease complications. Thus, imaging ATP molecule in both cellular and extracellular contexts has many applications in biology, engineering, and clinics. A sensitive and selective fluorescence “signal-on” probe for ATP detection was constructed, based on the base recognition between a black hole quencher (BHQ)-labeled aptamer oligonucleotide and a fluorophore (Cy5)-labeled reporter flare. The probe was able to detect ATP in solution with single digit µM detection limit. With the assistance of lipofectamine, this probe efficiently entered and shined in the model cells U2OS within 3 h. Further application of the probe in specific scenery, cardio-tissue engineering, was also tested where the ATP aptamer complex was able to sense cellular ATP status in a semi-quantitative manner, representing a novel approach for selection of functional cardiomyocytes for tissue engineering. At last a slight change in probe configuration in which a flexible intermolecular A14 linker was introduced granted regeneration capability. These data support the application of this probe in multiple circumstances where ATP measurement or imaging is on demand. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-021-05012-8. Springer Vienna 2021-09-23 2021 /pmc/articles/PMC8459148/ /pubmed/34554325 http://dx.doi.org/10.1007/s00604-021-05012-8 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Paper
Liu, Wenjun
Zhu, Xuena
Mozneb, Maedeh
Nagahara, Larry
Hu, Tony Y.
Li, Chen-Zhong
Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe
title Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe
title_full Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe
title_fullStr Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe
title_full_unstemmed Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe
title_short Lighting up ATP in cells and tissues using a simple aptamer-based fluorescent probe
title_sort lighting up atp in cells and tissues using a simple aptamer-based fluorescent probe
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459148/
https://www.ncbi.nlm.nih.gov/pubmed/34554325
http://dx.doi.org/10.1007/s00604-021-05012-8
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