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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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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. |
format | Online Article Text |
id | pubmed-5038762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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