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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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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. |
format | Online Article Text |
id | pubmed-4168480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lindenburglaurens engineeringgeneticallyencodedfretsensors AT merkxmaarten engineeringgeneticallyencodedfretsensors |