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The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods
Non-invasive fluorophore-based protein interaction assays like fluorescence resonance energy transfer (FRET) and bimolecular fluorescence complementation (BiFC, also referred to as "split YFP") have been proven invaluable tools to study protein-protein interactions in living cells. Both me...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1523328/ https://www.ncbi.nlm.nih.gov/pubmed/16800872 http://dx.doi.org/10.1186/1746-4811-2-12 |
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author | Bhat, Riyaz A Lahaye, Thomas Panstruga, Ralph |
author_facet | Bhat, Riyaz A Lahaye, Thomas Panstruga, Ralph |
author_sort | Bhat, Riyaz A |
collection | PubMed |
description | Non-invasive fluorophore-based protein interaction assays like fluorescence resonance energy transfer (FRET) and bimolecular fluorescence complementation (BiFC, also referred to as "split YFP") have been proven invaluable tools to study protein-protein interactions in living cells. Both methods are now frequently used in the plant sciences and are likely to develop into standard techniques for the identification, verification and in-depth analysis of polypeptide interactions. In this review, we address the individual strengths and weaknesses of both approaches and provide an outlook about new directions and possible future developments for both techniques. |
format | Text |
id | pubmed-1523328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15233282006-07-28 The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods Bhat, Riyaz A Lahaye, Thomas Panstruga, Ralph Plant Methods Review Non-invasive fluorophore-based protein interaction assays like fluorescence resonance energy transfer (FRET) and bimolecular fluorescence complementation (BiFC, also referred to as "split YFP") have been proven invaluable tools to study protein-protein interactions in living cells. Both methods are now frequently used in the plant sciences and are likely to develop into standard techniques for the identification, verification and in-depth analysis of polypeptide interactions. In this review, we address the individual strengths and weaknesses of both approaches and provide an outlook about new directions and possible future developments for both techniques. BioMed Central 2006-06-26 /pmc/articles/PMC1523328/ /pubmed/16800872 http://dx.doi.org/10.1186/1746-4811-2-12 Text en Copyright © 2006 Bhat et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Bhat, Riyaz A Lahaye, Thomas Panstruga, Ralph The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
title | The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
title_full | The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
title_fullStr | The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
title_full_unstemmed | The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
title_short | The visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
title_sort | visible touch: in planta visualization of protein-protein interactions by fluorophore-based methods |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1523328/ https://www.ncbi.nlm.nih.gov/pubmed/16800872 http://dx.doi.org/10.1186/1746-4811-2-12 |
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