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MMP-2/9-Specific Activatable Lifetime Imaging Agent
Optical (molecular) imaging can benefit from a combination of the high signal-to-background ratio of activatable fluorescence imaging with the high specificity of luminescence lifetime imaging. To allow for this combination, both imaging techniques were integrated in a single imaging agent, a so-cal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481940/ https://www.ncbi.nlm.nih.gov/pubmed/25985157 http://dx.doi.org/10.3390/s150511076 |
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author | Rood, Marcus T.M. Raspe, Marcel ten Hove, Jan Bart Jalink, Kees Velders, Aldrik H. van Leeuwen, Fijs W.B. |
author_facet | Rood, Marcus T.M. Raspe, Marcel ten Hove, Jan Bart Jalink, Kees Velders, Aldrik H. van Leeuwen, Fijs W.B. |
author_sort | Rood, Marcus T.M. |
collection | PubMed |
description | Optical (molecular) imaging can benefit from a combination of the high signal-to-background ratio of activatable fluorescence imaging with the high specificity of luminescence lifetime imaging. To allow for this combination, both imaging techniques were integrated in a single imaging agent, a so-called activatable lifetime imaging agent. Important in the design of this imaging agent is the use of two luminophores that are tethered by a specific peptide with a hairpin-motive that ensured close proximity of the two while also having a specific amino acid sequence available for enzymatic cleavage by tumor-related MMP-2/9. Ir(ppy)(3) and Cy5 were used because in close proximity the emission intensities of both luminophores were quenched and the influence of Cy5 shortens the Ir(ppy)(3) luminescence lifetime from 98 ns to 30 ns. Upon cleavage in vitro, both effects are undone, yielding an increase in Ir(ppy)(3) and Cy5 luminescence and a restoration of Ir(ppy)(3) luminescence lifetime to 94 ns. As a reference for the luminescence activation, a similar imaging agent with the more common Cy3-Cy5 fluorophore pair was used. Our findings underline that the combination of enzymatic signal activation with lifetime imaging is possible and that it provides a promising method in the design of future disease specific imaging agents. |
format | Online Article Text |
id | pubmed-4481940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44819402015-06-29 MMP-2/9-Specific Activatable Lifetime Imaging Agent Rood, Marcus T.M. Raspe, Marcel ten Hove, Jan Bart Jalink, Kees Velders, Aldrik H. van Leeuwen, Fijs W.B. Sensors (Basel) Article Optical (molecular) imaging can benefit from a combination of the high signal-to-background ratio of activatable fluorescence imaging with the high specificity of luminescence lifetime imaging. To allow for this combination, both imaging techniques were integrated in a single imaging agent, a so-called activatable lifetime imaging agent. Important in the design of this imaging agent is the use of two luminophores that are tethered by a specific peptide with a hairpin-motive that ensured close proximity of the two while also having a specific amino acid sequence available for enzymatic cleavage by tumor-related MMP-2/9. Ir(ppy)(3) and Cy5 were used because in close proximity the emission intensities of both luminophores were quenched and the influence of Cy5 shortens the Ir(ppy)(3) luminescence lifetime from 98 ns to 30 ns. Upon cleavage in vitro, both effects are undone, yielding an increase in Ir(ppy)(3) and Cy5 luminescence and a restoration of Ir(ppy)(3) luminescence lifetime to 94 ns. As a reference for the luminescence activation, a similar imaging agent with the more common Cy3-Cy5 fluorophore pair was used. Our findings underline that the combination of enzymatic signal activation with lifetime imaging is possible and that it provides a promising method in the design of future disease specific imaging agents. MDPI 2015-05-12 /pmc/articles/PMC4481940/ /pubmed/25985157 http://dx.doi.org/10.3390/s150511076 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rood, Marcus T.M. Raspe, Marcel ten Hove, Jan Bart Jalink, Kees Velders, Aldrik H. van Leeuwen, Fijs W.B. MMP-2/9-Specific Activatable Lifetime Imaging Agent |
title | MMP-2/9-Specific Activatable Lifetime Imaging Agent |
title_full | MMP-2/9-Specific Activatable Lifetime Imaging Agent |
title_fullStr | MMP-2/9-Specific Activatable Lifetime Imaging Agent |
title_full_unstemmed | MMP-2/9-Specific Activatable Lifetime Imaging Agent |
title_short | MMP-2/9-Specific Activatable Lifetime Imaging Agent |
title_sort | mmp-2/9-specific activatable lifetime imaging agent |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481940/ https://www.ncbi.nlm.nih.gov/pubmed/25985157 http://dx.doi.org/10.3390/s150511076 |
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