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Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging

To optimize live cell fluorescence imaging, the choice of fluorescent substrate is a critical factor. Although genetically encoded fluorescent proteins have been used widely, chemical fluorescent dyes are still useful when conjugated to proteins or ligands. However, little information is available f...

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Autores principales: Hayashi-Takanaka, Yoko, Stasevich, Timothy J., Kurumizaka, Hitoshi, Nozaki, Naohito, Kimura, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153647/
https://www.ncbi.nlm.nih.gov/pubmed/25184362
http://dx.doi.org/10.1371/journal.pone.0106271
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author Hayashi-Takanaka, Yoko
Stasevich, Timothy J.
Kurumizaka, Hitoshi
Nozaki, Naohito
Kimura, Hiroshi
author_facet Hayashi-Takanaka, Yoko
Stasevich, Timothy J.
Kurumizaka, Hitoshi
Nozaki, Naohito
Kimura, Hiroshi
author_sort Hayashi-Takanaka, Yoko
collection PubMed
description To optimize live cell fluorescence imaging, the choice of fluorescent substrate is a critical factor. Although genetically encoded fluorescent proteins have been used widely, chemical fluorescent dyes are still useful when conjugated to proteins or ligands. However, little information is available for the suitability of different fluorescent dyes for live imaging. We here systematically analyzed the property of a number of commercial fluorescent dyes when conjugated with antigen-binding (Fab) fragments directed against specific histone modifications, in particular, phosphorylated H3S28 (H3S28ph) and acetylated H3K9 (H3K9ac). These Fab fragments were conjugated with a fluorescent dye and loaded into living HeLa cells. H3S28ph-specific Fab fragments were expected to be enriched in condensed chromosomes, as H3S28 is phosphorylated during mitosis. However, the degree of Fab fragment enrichment on mitotic chromosomes varied depending on the conjugated dye. In general, green fluorescent dyes showed higher enrichment, compared to red and far-red fluorescent dyes, even when dye∶protein conjugation ratios were similar. These differences are partly explained by an altered affinity of Fab fragment after dye-conjugation; some dyes have less effect on the affinity, while others can affect it more. Moreover, red and far-red fluorescent dyes tended to form aggregates in the cytoplasm. Similar results were observed when H3K9ac-specific Fab fragments were used, suggesting that the properties of each dye affect different Fab fragments similarly. According to our analysis, conjugation with green fluorescent dyes, like Alexa Fluor 488 and Dylight 488, has the least effect on Fab affinity and is the best for live cell imaging, although these dyes are less photostable than red fluorescent dyes. When multicolor imaging is required, we recommend the following dye combinations for optimal results: Alexa Fluor 488 (green), Cy3 (red), and Cy5 or CF640 (far-red).
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spelling pubmed-41536472014-09-05 Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging Hayashi-Takanaka, Yoko Stasevich, Timothy J. Kurumizaka, Hitoshi Nozaki, Naohito Kimura, Hiroshi PLoS One Research Article To optimize live cell fluorescence imaging, the choice of fluorescent substrate is a critical factor. Although genetically encoded fluorescent proteins have been used widely, chemical fluorescent dyes are still useful when conjugated to proteins or ligands. However, little information is available for the suitability of different fluorescent dyes for live imaging. We here systematically analyzed the property of a number of commercial fluorescent dyes when conjugated with antigen-binding (Fab) fragments directed against specific histone modifications, in particular, phosphorylated H3S28 (H3S28ph) and acetylated H3K9 (H3K9ac). These Fab fragments were conjugated with a fluorescent dye and loaded into living HeLa cells. H3S28ph-specific Fab fragments were expected to be enriched in condensed chromosomes, as H3S28 is phosphorylated during mitosis. However, the degree of Fab fragment enrichment on mitotic chromosomes varied depending on the conjugated dye. In general, green fluorescent dyes showed higher enrichment, compared to red and far-red fluorescent dyes, even when dye∶protein conjugation ratios were similar. These differences are partly explained by an altered affinity of Fab fragment after dye-conjugation; some dyes have less effect on the affinity, while others can affect it more. Moreover, red and far-red fluorescent dyes tended to form aggregates in the cytoplasm. Similar results were observed when H3K9ac-specific Fab fragments were used, suggesting that the properties of each dye affect different Fab fragments similarly. According to our analysis, conjugation with green fluorescent dyes, like Alexa Fluor 488 and Dylight 488, has the least effect on Fab affinity and is the best for live cell imaging, although these dyes are less photostable than red fluorescent dyes. When multicolor imaging is required, we recommend the following dye combinations for optimal results: Alexa Fluor 488 (green), Cy3 (red), and Cy5 or CF640 (far-red). Public Library of Science 2014-09-03 /pmc/articles/PMC4153647/ /pubmed/25184362 http://dx.doi.org/10.1371/journal.pone.0106271 Text en © 2014 Hayashi-Takanaka et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hayashi-Takanaka, Yoko
Stasevich, Timothy J.
Kurumizaka, Hitoshi
Nozaki, Naohito
Kimura, Hiroshi
Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
title Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
title_full Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
title_fullStr Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
title_full_unstemmed Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
title_short Evaluation of Chemical Fluorescent Dyes as a Protein Conjugation Partner for Live Cell Imaging
title_sort evaluation of chemical fluorescent dyes as a protein conjugation partner for live cell imaging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153647/
https://www.ncbi.nlm.nih.gov/pubmed/25184362
http://dx.doi.org/10.1371/journal.pone.0106271
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