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A Guide to Fluorescent Protein FRET Pairs

Förster or fluorescence resonance energy transfer (FRET) technology and genetically encoded FRET biosensors provide a powerful tool for visualizing signaling molecules in live cells with high spatiotemporal resolution. Fluorescent proteins (FPs) are most commonly used as both donor and acceptor fluo...

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Detalles Bibliográficos
Autores principales: Bajar, Bryce T., Wang, Emily S., Zhang, Shu, Lin, Michael Z., Chu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038762/
https://www.ncbi.nlm.nih.gov/pubmed/27649177
http://dx.doi.org/10.3390/s16091488
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author Bajar, Bryce T.
Wang, Emily S.
Zhang, Shu
Lin, Michael Z.
Chu, Jun
author_facet Bajar, Bryce T.
Wang, Emily S.
Zhang, Shu
Lin, Michael Z.
Chu, Jun
author_sort Bajar, Bryce T.
collection PubMed
description Förster or fluorescence resonance energy transfer (FRET) technology and genetically encoded FRET biosensors provide a powerful tool for visualizing signaling molecules in live cells with high spatiotemporal resolution. Fluorescent proteins (FPs) are most commonly used as both donor and acceptor fluorophores in FRET biosensors, especially since FPs are genetically encodable and live-cell compatible. In this review, we will provide an overview of methods to measure FRET changes in biological contexts, discuss the palette of FP FRET pairs developed and their relative strengths and weaknesses, and note important factors to consider when using FPs for FRET studies.
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spelling pubmed-50387622016-09-29 A Guide to Fluorescent Protein FRET Pairs Bajar, Bryce T. Wang, Emily S. Zhang, Shu Lin, Michael Z. Chu, Jun Sensors (Basel) Review Förster or fluorescence resonance energy transfer (FRET) technology and genetically encoded FRET biosensors provide a powerful tool for visualizing signaling molecules in live cells with high spatiotemporal resolution. Fluorescent proteins (FPs) are most commonly used as both donor and acceptor fluorophores in FRET biosensors, especially since FPs are genetically encodable and live-cell compatible. In this review, we will provide an overview of methods to measure FRET changes in biological contexts, discuss the palette of FP FRET pairs developed and their relative strengths and weaknesses, and note important factors to consider when using FPs for FRET studies. MDPI 2016-09-14 /pmc/articles/PMC5038762/ /pubmed/27649177 http://dx.doi.org/10.3390/s16091488 Text en © 2016 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 (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bajar, Bryce T.
Wang, Emily S.
Zhang, Shu
Lin, Michael Z.
Chu, Jun
A Guide to Fluorescent Protein FRET Pairs
title A Guide to Fluorescent Protein FRET Pairs
title_full A Guide to Fluorescent Protein FRET Pairs
title_fullStr A Guide to Fluorescent Protein FRET Pairs
title_full_unstemmed A Guide to Fluorescent Protein FRET Pairs
title_short A Guide to Fluorescent Protein FRET Pairs
title_sort guide to fluorescent protein fret pairs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038762/
https://www.ncbi.nlm.nih.gov/pubmed/27649177
http://dx.doi.org/10.3390/s16091488
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