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Fluorogen-activating proteins: beyond classical fluorescent proteins

Fluorescence imaging is a powerful technique for the real-time noninvasive monitoring of protein dynamics. Recently, fluorogen activating proteins (FAPs)/fluorogen probes for protein imaging were developed. Unlike the traditional fluorescent proteins (FPs), FAPs do not fluoresce unless bound to thei...

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Detalles Bibliográficos
Autores principales: Xu, Shengnan, Hu, Hai-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989828/
https://www.ncbi.nlm.nih.gov/pubmed/29881673
http://dx.doi.org/10.1016/j.apsb.2018.02.001
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author Xu, Shengnan
Hu, Hai-Yu
author_facet Xu, Shengnan
Hu, Hai-Yu
author_sort Xu, Shengnan
collection PubMed
description Fluorescence imaging is a powerful technique for the real-time noninvasive monitoring of protein dynamics. Recently, fluorogen activating proteins (FAPs)/fluorogen probes for protein imaging were developed. Unlike the traditional fluorescent proteins (FPs), FAPs do not fluoresce unless bound to their specific small-molecule fluorogens. When using FAPs/fluorogen probes, a washing step is not required for the removal of free probes from the cells, thus allowing rapid and specific detection of proteins in living cells with high signal-to-noise ratio. Furthermore, with different fluorogens, living cell multi-color proteins labeling system was developed. In this review, we describe about the discovery of FAPs, the design strategy of FAP fluorogens, the application of the FAP technology and the advances of FAP technology in protein labeling systems.
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spelling pubmed-59898282018-06-07 Fluorogen-activating proteins: beyond classical fluorescent proteins Xu, Shengnan Hu, Hai-Yu Acta Pharm Sin B Review Fluorescence imaging is a powerful technique for the real-time noninvasive monitoring of protein dynamics. Recently, fluorogen activating proteins (FAPs)/fluorogen probes for protein imaging were developed. Unlike the traditional fluorescent proteins (FPs), FAPs do not fluoresce unless bound to their specific small-molecule fluorogens. When using FAPs/fluorogen probes, a washing step is not required for the removal of free probes from the cells, thus allowing rapid and specific detection of proteins in living cells with high signal-to-noise ratio. Furthermore, with different fluorogens, living cell multi-color proteins labeling system was developed. In this review, we describe about the discovery of FAPs, the design strategy of FAP fluorogens, the application of the FAP technology and the advances of FAP technology in protein labeling systems. Elsevier 2018-05 2018-03-24 /pmc/articles/PMC5989828/ /pubmed/29881673 http://dx.doi.org/10.1016/j.apsb.2018.02.001 Text en © 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Xu, Shengnan
Hu, Hai-Yu
Fluorogen-activating proteins: beyond classical fluorescent proteins
title Fluorogen-activating proteins: beyond classical fluorescent proteins
title_full Fluorogen-activating proteins: beyond classical fluorescent proteins
title_fullStr Fluorogen-activating proteins: beyond classical fluorescent proteins
title_full_unstemmed Fluorogen-activating proteins: beyond classical fluorescent proteins
title_short Fluorogen-activating proteins: beyond classical fluorescent proteins
title_sort fluorogen-activating proteins: beyond classical fluorescent proteins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989828/
https://www.ncbi.nlm.nih.gov/pubmed/29881673
http://dx.doi.org/10.1016/j.apsb.2018.02.001
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