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A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy

Simultaneous visualization and concentration quantification of molecules in biological tissue is an important though challenging goal. The advantages of fluorescence lifetime imaging microscopy (FLIM) for visualization, and electron paramagnetic resonance (EPR) spectroscopy for quantification are co...

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Autores principales: Dong, Pin, Stellmacher, Johannes, Bouchet, Lydia M., Nieke, Marius, Kumar, Amit, Osorio‐Blanco, Ernesto R., Nagel, Gregor, Lohan, Silke B., Teutloff, Christian, Patzelt, Alexa, Schäfer‐Korting, Monika, Calderón, Marcelo, Meinke, Martina C., Alexiev, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251738/
https://www.ncbi.nlm.nih.gov/pubmed/33544452
http://dx.doi.org/10.1002/anie.202012852
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author Dong, Pin
Stellmacher, Johannes
Bouchet, Lydia M.
Nieke, Marius
Kumar, Amit
Osorio‐Blanco, Ernesto R.
Nagel, Gregor
Lohan, Silke B.
Teutloff, Christian
Patzelt, Alexa
Schäfer‐Korting, Monika
Calderón, Marcelo
Meinke, Martina C.
Alexiev, Ulrike
author_facet Dong, Pin
Stellmacher, Johannes
Bouchet, Lydia M.
Nieke, Marius
Kumar, Amit
Osorio‐Blanco, Ernesto R.
Nagel, Gregor
Lohan, Silke B.
Teutloff, Christian
Patzelt, Alexa
Schäfer‐Korting, Monika
Calderón, Marcelo
Meinke, Martina C.
Alexiev, Ulrike
author_sort Dong, Pin
collection PubMed
description Simultaneous visualization and concentration quantification of molecules in biological tissue is an important though challenging goal. The advantages of fluorescence lifetime imaging microscopy (FLIM) for visualization, and electron paramagnetic resonance (EPR) spectroscopy for quantification are complementary. Their combination in a multiplexed approach promises a successful but ambitious strategy because of spin label‐mediated fluorescence quenching. Here, we solved this problem and present the molecular design of a dual label (DL) compound comprising a highly fluorescent dye together with an EPR spin probe, which also renders the fluorescence lifetime to be concentration sensitive. The DL can easily be coupled to the biomolecule of choice, enabling in vivo and in vitro applications. This novel approach paves the way for elegant studies ranging from fundamental biological investigations to preclinical drug research, as shown in proof‐of‐principle penetration experiments in human skin ex vivo.
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spelling pubmed-82517382021-07-07 A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy Dong, Pin Stellmacher, Johannes Bouchet, Lydia M. Nieke, Marius Kumar, Amit Osorio‐Blanco, Ernesto R. Nagel, Gregor Lohan, Silke B. Teutloff, Christian Patzelt, Alexa Schäfer‐Korting, Monika Calderón, Marcelo Meinke, Martina C. Alexiev, Ulrike Angew Chem Int Ed Engl Research Articles Simultaneous visualization and concentration quantification of molecules in biological tissue is an important though challenging goal. The advantages of fluorescence lifetime imaging microscopy (FLIM) for visualization, and electron paramagnetic resonance (EPR) spectroscopy for quantification are complementary. Their combination in a multiplexed approach promises a successful but ambitious strategy because of spin label‐mediated fluorescence quenching. Here, we solved this problem and present the molecular design of a dual label (DL) compound comprising a highly fluorescent dye together with an EPR spin probe, which also renders the fluorescence lifetime to be concentration sensitive. The DL can easily be coupled to the biomolecule of choice, enabling in vivo and in vitro applications. This novel approach paves the way for elegant studies ranging from fundamental biological investigations to preclinical drug research, as shown in proof‐of‐principle penetration experiments in human skin ex vivo. John Wiley and Sons Inc. 2021-05-26 2021-06-25 /pmc/articles/PMC8251738/ /pubmed/33544452 http://dx.doi.org/10.1002/anie.202012852 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Dong, Pin
Stellmacher, Johannes
Bouchet, Lydia M.
Nieke, Marius
Kumar, Amit
Osorio‐Blanco, Ernesto R.
Nagel, Gregor
Lohan, Silke B.
Teutloff, Christian
Patzelt, Alexa
Schäfer‐Korting, Monika
Calderón, Marcelo
Meinke, Martina C.
Alexiev, Ulrike
A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy
title A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy
title_full A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy
title_fullStr A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy
title_full_unstemmed A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy
title_short A Dual Fluorescence–Spin Label Probe for Visualization and Quantification of Target Molecules in Tissue by Multiplexed FLIM–EPR Spectroscopy
title_sort dual fluorescence–spin label probe for visualization and quantification of target molecules in tissue by multiplexed flim–epr spectroscopy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251738/
https://www.ncbi.nlm.nih.gov/pubmed/33544452
http://dx.doi.org/10.1002/anie.202012852
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