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Engineering Genetically Encoded FRET Sensors

Förster Resonance Energy Transfer (FRET) between two fluorescent proteins can be exploited to create fully genetically encoded and thus subcellularly targetable sensors. FRET sensors report changes in energy transfer between a donor and an acceptor fluorescent protein that occur when an attached sen...

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Detalles Bibliográficos
Autores principales: Lindenburg, Laurens, Merkx, Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168480/
https://www.ncbi.nlm.nih.gov/pubmed/24991940
http://dx.doi.org/10.3390/s140711691
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author Lindenburg, Laurens
Merkx, Maarten
author_facet Lindenburg, Laurens
Merkx, Maarten
author_sort Lindenburg, Laurens
collection PubMed
description Förster Resonance Energy Transfer (FRET) between two fluorescent proteins can be exploited to create fully genetically encoded and thus subcellularly targetable sensors. FRET sensors report changes in energy transfer between a donor and an acceptor fluorescent protein that occur when an attached sensor domain undergoes a change in conformation in response to ligand binding. The design of sensitive FRET sensors remains challenging as there are few generally applicable design rules and each sensor must be optimized anew. In this review we discuss various strategies that address this shortcoming, including rational design approaches that exploit self-associating fluorescent domains and the directed evolution of FRET sensors using high-throughput screening.
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spelling pubmed-41684802014-09-19 Engineering Genetically Encoded FRET Sensors Lindenburg, Laurens Merkx, Maarten Sensors (Basel) Article Förster Resonance Energy Transfer (FRET) between two fluorescent proteins can be exploited to create fully genetically encoded and thus subcellularly targetable sensors. FRET sensors report changes in energy transfer between a donor and an acceptor fluorescent protein that occur when an attached sensor domain undergoes a change in conformation in response to ligand binding. The design of sensitive FRET sensors remains challenging as there are few generally applicable design rules and each sensor must be optimized anew. In this review we discuss various strategies that address this shortcoming, including rational design approaches that exploit self-associating fluorescent domains and the directed evolution of FRET sensors using high-throughput screening. MDPI 2014-07-02 /pmc/articles/PMC4168480/ /pubmed/24991940 http://dx.doi.org/10.3390/s140711691 Text en © 2014 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/3.0/).
spellingShingle Article
Lindenburg, Laurens
Merkx, Maarten
Engineering Genetically Encoded FRET Sensors
title Engineering Genetically Encoded FRET Sensors
title_full Engineering Genetically Encoded FRET Sensors
title_fullStr Engineering Genetically Encoded FRET Sensors
title_full_unstemmed Engineering Genetically Encoded FRET Sensors
title_short Engineering Genetically Encoded FRET Sensors
title_sort engineering genetically encoded fret sensors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168480/
https://www.ncbi.nlm.nih.gov/pubmed/24991940
http://dx.doi.org/10.3390/s140711691
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