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A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag
BACKGROUND: In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal labeling offers an elegant way for direct labeling of proteins in live cells with fluorescent dyes. This labeling approach is currently not broadly used in live-cell applications, partly because it ne...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961407/ https://www.ncbi.nlm.nih.gov/pubmed/31937312 http://dx.doi.org/10.1186/s12915-019-0708-7 |
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author | Segal, Inbar Nachmias, Dikla Konig, Andres Alon, Ariel Arbely, Eyal Elia, Natalie |
author_facet | Segal, Inbar Nachmias, Dikla Konig, Andres Alon, Ariel Arbely, Eyal Elia, Natalie |
author_sort | Segal, Inbar |
collection | PubMed |
description | BACKGROUND: In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal labeling offers an elegant way for direct labeling of proteins in live cells with fluorescent dyes. This labeling approach is currently not broadly used in live-cell applications, partly because it needs to be adjusted to the specific protein under study. RESULTS: We present a generic, 14-residue long, N-terminal tag for GCE-based labeling of proteins in live mammalian cells. Using this tag, we generated a library of GCE-based organelle markers, demonstrating the applicability of the tag for labeling a plethora of proteins and organelles. Finally, we show that the HA epitope, used as a backbone in our tag, may be substituted with other epitopes and, in some cases, can be completely removed, reducing the tag length to 5 residues. CONCLUSIONS: The GCE-tag presented here offers a powerful, easy-to-implement tool for live-cell labeling of cellular proteins with small and bright probes. |
format | Online Article Text |
id | pubmed-6961407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69614072020-01-17 A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag Segal, Inbar Nachmias, Dikla Konig, Andres Alon, Ariel Arbely, Eyal Elia, Natalie BMC Biol Methodology Article BACKGROUND: In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal labeling offers an elegant way for direct labeling of proteins in live cells with fluorescent dyes. This labeling approach is currently not broadly used in live-cell applications, partly because it needs to be adjusted to the specific protein under study. RESULTS: We present a generic, 14-residue long, N-terminal tag for GCE-based labeling of proteins in live mammalian cells. Using this tag, we generated a library of GCE-based organelle markers, demonstrating the applicability of the tag for labeling a plethora of proteins and organelles. Finally, we show that the HA epitope, used as a backbone in our tag, may be substituted with other epitopes and, in some cases, can be completely removed, reducing the tag length to 5 residues. CONCLUSIONS: The GCE-tag presented here offers a powerful, easy-to-implement tool for live-cell labeling of cellular proteins with small and bright probes. BioMed Central 2020-01-14 /pmc/articles/PMC6961407/ /pubmed/31937312 http://dx.doi.org/10.1186/s12915-019-0708-7 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Segal, Inbar Nachmias, Dikla Konig, Andres Alon, Ariel Arbely, Eyal Elia, Natalie A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
title | A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
title_full | A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
title_fullStr | A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
title_full_unstemmed | A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
title_short | A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
title_sort | straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961407/ https://www.ncbi.nlm.nih.gov/pubmed/31937312 http://dx.doi.org/10.1186/s12915-019-0708-7 |
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