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A new twist on PIFE: photoisomerisation-related fluorescence enhancement
PIFE was first used as an acronym for protein-induced fluorescence enhancement, which refers to the increase in fluorescence observed upon the interaction of a fluorophore, such as a cyanine, with a protein. This fluorescence enhancement is due to changes in the rate of cis/trans photoisomerisation....
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOP Publishing
2024
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570931/ https://www.ncbi.nlm.nih.gov/pubmed/37726007 http://dx.doi.org/10.1088/2050-6120/acfb58 |
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author | Ploetz, Evelyn Ambrose, Benjamin Barth, Anders Börner, Richard Erichson, Felix Kapanidis, Achillefs N Kim, Harold D Levitus, Marcia Lohman, Timothy M Mazumder, Abhishek Rueda, David S Steffen, Fabio D Cordes, Thorben Magennis, Steven W Lerner, Eitan |
author_facet | Ploetz, Evelyn Ambrose, Benjamin Barth, Anders Börner, Richard Erichson, Felix Kapanidis, Achillefs N Kim, Harold D Levitus, Marcia Lohman, Timothy M Mazumder, Abhishek Rueda, David S Steffen, Fabio D Cordes, Thorben Magennis, Steven W Lerner, Eitan |
author_sort | Ploetz, Evelyn |
collection | PubMed |
description | PIFE was first used as an acronym for protein-induced fluorescence enhancement, which refers to the increase in fluorescence observed upon the interaction of a fluorophore, such as a cyanine, with a protein. This fluorescence enhancement is due to changes in the rate of cis/trans photoisomerisation. It is clear now that this mechanism is generally applicable to interactions with any biomolecule. In this review, we propose that PIFE is thereby renamed according to its fundamental working principle as photoisomerisation-related fluorescence enhancement, keeping the PIFE acronym intact. We discuss the photochemistry of cyanine fluorophores, the mechanism of PIFE, its advantages and limitations, and recent approaches to turning PIFE into a quantitative assay. We provide an overview of its current applications to different biomolecules and discuss potential future uses, including the study of protein-protein interactions, protein-ligand interactions and conformational changes in biomolecules. |
format | Online Article Text |
id | pubmed-10570931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2024 |
publisher | IOP Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-105709312023-10-14 A new twist on PIFE: photoisomerisation-related fluorescence enhancement Ploetz, Evelyn Ambrose, Benjamin Barth, Anders Börner, Richard Erichson, Felix Kapanidis, Achillefs N Kim, Harold D Levitus, Marcia Lohman, Timothy M Mazumder, Abhishek Rueda, David S Steffen, Fabio D Cordes, Thorben Magennis, Steven W Lerner, Eitan Methods Appl Fluoresc Topical Review PIFE was first used as an acronym for protein-induced fluorescence enhancement, which refers to the increase in fluorescence observed upon the interaction of a fluorophore, such as a cyanine, with a protein. This fluorescence enhancement is due to changes in the rate of cis/trans photoisomerisation. It is clear now that this mechanism is generally applicable to interactions with any biomolecule. In this review, we propose that PIFE is thereby renamed according to its fundamental working principle as photoisomerisation-related fluorescence enhancement, keeping the PIFE acronym intact. We discuss the photochemistry of cyanine fluorophores, the mechanism of PIFE, its advantages and limitations, and recent approaches to turning PIFE into a quantitative assay. We provide an overview of its current applications to different biomolecules and discuss potential future uses, including the study of protein-protein interactions, protein-ligand interactions and conformational changes in biomolecules. IOP Publishing 2024-01-01 2023-10-12 /pmc/articles/PMC10570931/ /pubmed/37726007 http://dx.doi.org/10.1088/2050-6120/acfb58 Text en © 2023 The Author(s). Published by IOP Publishing Ltd https://creativecommons.org/licenses/by/4.0/Original content from this work may be used under the terms of the Creative Commons Attribution 4.0 licence (https://creativecommons.org/licenses/by/4.0/) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI. |
spellingShingle | Topical Review Ploetz, Evelyn Ambrose, Benjamin Barth, Anders Börner, Richard Erichson, Felix Kapanidis, Achillefs N Kim, Harold D Levitus, Marcia Lohman, Timothy M Mazumder, Abhishek Rueda, David S Steffen, Fabio D Cordes, Thorben Magennis, Steven W Lerner, Eitan A new twist on PIFE: photoisomerisation-related fluorescence enhancement |
title | A new twist on PIFE: photoisomerisation-related fluorescence enhancement |
title_full | A new twist on PIFE: photoisomerisation-related fluorescence enhancement |
title_fullStr | A new twist on PIFE: photoisomerisation-related fluorescence enhancement |
title_full_unstemmed | A new twist on PIFE: photoisomerisation-related fluorescence enhancement |
title_short | A new twist on PIFE: photoisomerisation-related fluorescence enhancement |
title_sort | new twist on pife: photoisomerisation-related fluorescence enhancement |
topic | Topical Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570931/ https://www.ncbi.nlm.nih.gov/pubmed/37726007 http://dx.doi.org/10.1088/2050-6120/acfb58 |
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