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A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies

Epitope tagging is a versatile approach to study different proteins using a well-defined and established methodology. To date, most epitope tags such as myc, HA, V5 and FLAG tags are recognized by antibodies, which limits their use to fixed cells, tissues or protein samples. Here we introduce a broa...

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Autores principales: Traenkle, Bjoern, Segan, Sören, Fagbadebo, Funmilayo O., Kaiser, Philipp D., Rothbauer, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459311/
https://www.ncbi.nlm.nih.gov/pubmed/32868807
http://dx.doi.org/10.1038/s41598-020-71091-x
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author Traenkle, Bjoern
Segan, Sören
Fagbadebo, Funmilayo O.
Kaiser, Philipp D.
Rothbauer, Ulrich
author_facet Traenkle, Bjoern
Segan, Sören
Fagbadebo, Funmilayo O.
Kaiser, Philipp D.
Rothbauer, Ulrich
author_sort Traenkle, Bjoern
collection PubMed
description Epitope tagging is a versatile approach to study different proteins using a well-defined and established methodology. To date, most epitope tags such as myc, HA, V5 and FLAG tags are recognized by antibodies, which limits their use to fixed cells, tissues or protein samples. Here we introduce a broadly applicable tagging strategy utilizing a short peptide tag (PepTag) which is specifically recognized by a nanobody (PepNB). We demonstrated that the PepNB can be easily functionalized for immunoprecipitation or direct immunofluorescence staining of Pep-tagged proteins in vitro. For in cellulo studies we converted the PepNB into a fluorescently labeled Pep-chromobody (PepCB) which is functionally expressed in living cells. The addition of the small PepTag does not interfere with the examined structures in different cellular compartments and its detection with the PepCB enables optical antigen tracing in real time. By employing the phenomenon of antigen-mediated chromobody stabilization (AMCBS) using a turnover-accelerated PepCB we demonstrated that the system is suitable to visualize and quantify changes in Pep-tagged antigen concentration by quantitative live-cell imaging. We expect that this novel tagging strategy offers new opportunities to study the dynamic regulation of proteins, e.g. during cellular signaling, cell differentiation, or upon drug action.
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spelling pubmed-74593112020-09-01 A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies Traenkle, Bjoern Segan, Sören Fagbadebo, Funmilayo O. Kaiser, Philipp D. Rothbauer, Ulrich Sci Rep Article Epitope tagging is a versatile approach to study different proteins using a well-defined and established methodology. To date, most epitope tags such as myc, HA, V5 and FLAG tags are recognized by antibodies, which limits their use to fixed cells, tissues or protein samples. Here we introduce a broadly applicable tagging strategy utilizing a short peptide tag (PepTag) which is specifically recognized by a nanobody (PepNB). We demonstrated that the PepNB can be easily functionalized for immunoprecipitation or direct immunofluorescence staining of Pep-tagged proteins in vitro. For in cellulo studies we converted the PepNB into a fluorescently labeled Pep-chromobody (PepCB) which is functionally expressed in living cells. The addition of the small PepTag does not interfere with the examined structures in different cellular compartments and its detection with the PepCB enables optical antigen tracing in real time. By employing the phenomenon of antigen-mediated chromobody stabilization (AMCBS) using a turnover-accelerated PepCB we demonstrated that the system is suitable to visualize and quantify changes in Pep-tagged antigen concentration by quantitative live-cell imaging. We expect that this novel tagging strategy offers new opportunities to study the dynamic regulation of proteins, e.g. during cellular signaling, cell differentiation, or upon drug action. Nature Publishing Group UK 2020-08-31 /pmc/articles/PMC7459311/ /pubmed/32868807 http://dx.doi.org/10.1038/s41598-020-71091-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Traenkle, Bjoern
Segan, Sören
Fagbadebo, Funmilayo O.
Kaiser, Philipp D.
Rothbauer, Ulrich
A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
title A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
title_full A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
title_fullStr A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
title_full_unstemmed A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
title_short A novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
title_sort novel epitope tagging system to visualize and monitor antigens in live cells with chromobodies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459311/
https://www.ncbi.nlm.nih.gov/pubmed/32868807
http://dx.doi.org/10.1038/s41598-020-71091-x
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