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Bright GFP with subnanosecond fluorescence lifetime

Fluorescence lifetime imaging microscopy (FLIM) measures fluorescence decay rate at every pixel of an image. FLIM can separate probes of the same color but different fluorescence lifetimes (FL), thus it is a promising approach for multiparameter imaging. However, available GFP-like fluorescent prote...

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Autores principales: Mamontova, Anastasia V., Solovyev, Ilya D., Savitsky, Alexander P., Shakhov, Alexander М., Lukyanov, Konstantin A., Bogdanov, Alexey M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125319/
https://www.ncbi.nlm.nih.gov/pubmed/30185895
http://dx.doi.org/10.1038/s41598-018-31687-w
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author Mamontova, Anastasia V.
Solovyev, Ilya D.
Savitsky, Alexander P.
Shakhov, Alexander М.
Lukyanov, Konstantin A.
Bogdanov, Alexey M.
author_facet Mamontova, Anastasia V.
Solovyev, Ilya D.
Savitsky, Alexander P.
Shakhov, Alexander М.
Lukyanov, Konstantin A.
Bogdanov, Alexey M.
author_sort Mamontova, Anastasia V.
collection PubMed
description Fluorescence lifetime imaging microscopy (FLIM) measures fluorescence decay rate at every pixel of an image. FLIM can separate probes of the same color but different fluorescence lifetimes (FL), thus it is a promising approach for multiparameter imaging. However, available GFP-like fluorescent proteins (FP) possess a narrow range of FLs (commonly, 2.3–3.5 ns) which limits their applicability for multiparameter FLIM. Here we report a new FP probe showing both subnanosecond fluorescence lifetime and exceptional fluorescence brightness (80% of EGFP). To design this probe we applied semi-rational amino acid substitutions selection. Critical positions (Thr65, Tyr145, Phe165) were altered based on previously reported effect on FL or excited state electron transfer. The resulting EGFP triple mutant, BrUSLEE (Bright Ultimately Short Lifetime Enhanced Emitter), allows for both reliable detection of the probe and recording FL signal clearly distinguishable from that of the spectrally similar commonly used GFPs. We demonstrated high performance of this probe in multiparameter FLIM experiment. We suggest that amino acid substitutions described here lead to a significant shift in radiative and non-radiative excited state processes equilibrium.
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spelling pubmed-61253192018-09-10 Bright GFP with subnanosecond fluorescence lifetime Mamontova, Anastasia V. Solovyev, Ilya D. Savitsky, Alexander P. Shakhov, Alexander М. Lukyanov, Konstantin A. Bogdanov, Alexey M. Sci Rep Article Fluorescence lifetime imaging microscopy (FLIM) measures fluorescence decay rate at every pixel of an image. FLIM can separate probes of the same color but different fluorescence lifetimes (FL), thus it is a promising approach for multiparameter imaging. However, available GFP-like fluorescent proteins (FP) possess a narrow range of FLs (commonly, 2.3–3.5 ns) which limits their applicability for multiparameter FLIM. Here we report a new FP probe showing both subnanosecond fluorescence lifetime and exceptional fluorescence brightness (80% of EGFP). To design this probe we applied semi-rational amino acid substitutions selection. Critical positions (Thr65, Tyr145, Phe165) were altered based on previously reported effect on FL or excited state electron transfer. The resulting EGFP triple mutant, BrUSLEE (Bright Ultimately Short Lifetime Enhanced Emitter), allows for both reliable detection of the probe and recording FL signal clearly distinguishable from that of the spectrally similar commonly used GFPs. We demonstrated high performance of this probe in multiparameter FLIM experiment. We suggest that amino acid substitutions described here lead to a significant shift in radiative and non-radiative excited state processes equilibrium. Nature Publishing Group UK 2018-09-05 /pmc/articles/PMC6125319/ /pubmed/30185895 http://dx.doi.org/10.1038/s41598-018-31687-w Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mamontova, Anastasia V.
Solovyev, Ilya D.
Savitsky, Alexander P.
Shakhov, Alexander М.
Lukyanov, Konstantin A.
Bogdanov, Alexey M.
Bright GFP with subnanosecond fluorescence lifetime
title Bright GFP with subnanosecond fluorescence lifetime
title_full Bright GFP with subnanosecond fluorescence lifetime
title_fullStr Bright GFP with subnanosecond fluorescence lifetime
title_full_unstemmed Bright GFP with subnanosecond fluorescence lifetime
title_short Bright GFP with subnanosecond fluorescence lifetime
title_sort bright gfp with subnanosecond fluorescence lifetime
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125319/
https://www.ncbi.nlm.nih.gov/pubmed/30185895
http://dx.doi.org/10.1038/s41598-018-31687-w
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