Cargando…

Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase

BACKGROUND: Despite a plethora of bioluminescent reporter genes being cloned and used for cell assays and molecular imaging purposes, the simultaneous monitoring of multiple events in small animals is still challenging. This is partly attributable to the lack of optimization of cell reporter gene ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Mezzanotte, Laura, Que, Ivo, Kaijzel, Eric, Branchini, Bruce, Roda, Aldo, Löwik, Clemens
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081340/
https://www.ncbi.nlm.nih.gov/pubmed/21544210
http://dx.doi.org/10.1371/journal.pone.0019277
_version_ 1782202204066676736
author Mezzanotte, Laura
Que, Ivo
Kaijzel, Eric
Branchini, Bruce
Roda, Aldo
Löwik, Clemens
author_facet Mezzanotte, Laura
Que, Ivo
Kaijzel, Eric
Branchini, Bruce
Roda, Aldo
Löwik, Clemens
author_sort Mezzanotte, Laura
collection PubMed
description BACKGROUND: Despite a plethora of bioluminescent reporter genes being cloned and used for cell assays and molecular imaging purposes, the simultaneous monitoring of multiple events in small animals is still challenging. This is partly attributable to the lack of optimization of cell reporter gene expression as well as too much spectral overlap of the color-coupled reporter genes. A new red emitting codon-optimized luciferase reporter gene mutant of Photinus pyralis, Ppy RE8, has been developed and used in combination with the green click beetle luciferase, CBG99. PRINCIPAL FINDINGS: Human embryonic kidney cells (HEK293) were transfected with vectors that expressed red Ppy RE8 and green CBG99 luciferases. Populations of red and green emitting cells were mixed in different ratios. After addition of the shared single substrate, D-luciferin, bioluminescent (BL) signals were imaged with an ultrasensitive cooled CCD camera using a series of band pass filters (20 nm). Spectral unmixing algorithms were applied to the images where good separation of signals was observed. Furthermore, HEK293 cells that expressed the two luciferases were injected at different depth in the animals. Spectrally-separate images and quantification of the dual BL signals in a mixed population of cells was achieved when cells were either injected subcutaneously or directly into the prostate. SIGNIFICANCE: We report here the re-engineering of different luciferase genes for in vitro and in vivo dual color imaging applications to address the technical issues of using dual luciferases for imaging. In respect to previously used dual assays, our study demonstrated enhanced sensitivity combined with spatially separate BL spectral emissions using a suitable spectral unmixing algorithm. This new D-luciferin-dependent reporter gene couplet opens up the possibility in the future for more accurate quantitative gene expression studies in vivo by simultaneously monitoring two events in real time.
format Text
id pubmed-3081340
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-30813402011-05-04 Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase Mezzanotte, Laura Que, Ivo Kaijzel, Eric Branchini, Bruce Roda, Aldo Löwik, Clemens PLoS One Research Article BACKGROUND: Despite a plethora of bioluminescent reporter genes being cloned and used for cell assays and molecular imaging purposes, the simultaneous monitoring of multiple events in small animals is still challenging. This is partly attributable to the lack of optimization of cell reporter gene expression as well as too much spectral overlap of the color-coupled reporter genes. A new red emitting codon-optimized luciferase reporter gene mutant of Photinus pyralis, Ppy RE8, has been developed and used in combination with the green click beetle luciferase, CBG99. PRINCIPAL FINDINGS: Human embryonic kidney cells (HEK293) were transfected with vectors that expressed red Ppy RE8 and green CBG99 luciferases. Populations of red and green emitting cells were mixed in different ratios. After addition of the shared single substrate, D-luciferin, bioluminescent (BL) signals were imaged with an ultrasensitive cooled CCD camera using a series of band pass filters (20 nm). Spectral unmixing algorithms were applied to the images where good separation of signals was observed. Furthermore, HEK293 cells that expressed the two luciferases were injected at different depth in the animals. Spectrally-separate images and quantification of the dual BL signals in a mixed population of cells was achieved when cells were either injected subcutaneously or directly into the prostate. SIGNIFICANCE: We report here the re-engineering of different luciferase genes for in vitro and in vivo dual color imaging applications to address the technical issues of using dual luciferases for imaging. In respect to previously used dual assays, our study demonstrated enhanced sensitivity combined with spatially separate BL spectral emissions using a suitable spectral unmixing algorithm. This new D-luciferin-dependent reporter gene couplet opens up the possibility in the future for more accurate quantitative gene expression studies in vivo by simultaneously monitoring two events in real time. Public Library of Science 2011-04-22 /pmc/articles/PMC3081340/ /pubmed/21544210 http://dx.doi.org/10.1371/journal.pone.0019277 Text en Mezzanotte 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
Mezzanotte, Laura
Que, Ivo
Kaijzel, Eric
Branchini, Bruce
Roda, Aldo
Löwik, Clemens
Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase
title Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase
title_full Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase
title_fullStr Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase
title_full_unstemmed Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase
title_short Sensitive Dual Color In Vivo Bioluminescence Imaging Using a New Red Codon Optimized Firefly Luciferase and a Green Click Beetle Luciferase
title_sort sensitive dual color in vivo bioluminescence imaging using a new red codon optimized firefly luciferase and a green click beetle luciferase
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081340/
https://www.ncbi.nlm.nih.gov/pubmed/21544210
http://dx.doi.org/10.1371/journal.pone.0019277
work_keys_str_mv AT mezzanottelaura sensitivedualcolorinvivobioluminescenceimagingusinganewredcodonoptimizedfireflyluciferaseandagreenclickbeetleluciferase
AT queivo sensitivedualcolorinvivobioluminescenceimagingusinganewredcodonoptimizedfireflyluciferaseandagreenclickbeetleluciferase
AT kaijzeleric sensitivedualcolorinvivobioluminescenceimagingusinganewredcodonoptimizedfireflyluciferaseandagreenclickbeetleluciferase
AT branchinibruce sensitivedualcolorinvivobioluminescenceimagingusinganewredcodonoptimizedfireflyluciferaseandagreenclickbeetleluciferase
AT rodaaldo sensitivedualcolorinvivobioluminescenceimagingusinganewredcodonoptimizedfireflyluciferaseandagreenclickbeetleluciferase
AT lowikclemens sensitivedualcolorinvivobioluminescenceimagingusinganewredcodonoptimizedfireflyluciferaseandagreenclickbeetleluciferase