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Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy
Antibody conjugates have taken a great leap forward as tools in basic and applied molecular life sciences that was enabled by the development of chemoselective reactions for the site‐specific modification of proteins. Antibody‐oligonucleotide conjugates combine the antibody's target specificity...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048457/ https://www.ncbi.nlm.nih.gov/pubmed/33207032 http://dx.doi.org/10.1002/cbic.202000727 |
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author | Schwach, Jonathan Kolobynina, Ksenia Brandstetter, Katharina Gerlach, Marcus Ochtrop, Philipp Helma, Jonas Hackenberger, Christian P. R. Harz, Hartmann Cardoso, M. Cristina Leonhardt, Heinrich Stengl, Andreas |
author_facet | Schwach, Jonathan Kolobynina, Ksenia Brandstetter, Katharina Gerlach, Marcus Ochtrop, Philipp Helma, Jonas Hackenberger, Christian P. R. Harz, Hartmann Cardoso, M. Cristina Leonhardt, Heinrich Stengl, Andreas |
author_sort | Schwach, Jonathan |
collection | PubMed |
description | Antibody conjugates have taken a great leap forward as tools in basic and applied molecular life sciences that was enabled by the development of chemoselective reactions for the site‐specific modification of proteins. Antibody‐oligonucleotide conjugates combine the antibody's target specificity with the reversible, sequence‐encoded binding properties of oligonucleotides like DNAs or peptide nucleic acids (PNAs), allowing sequential imaging of large numbers of targets in a single specimen. In this report, we use the Tub‐tag® technology in combination with Cu‐catalyzed azide‐alkyne cycloaddition for the site‐specific conjugation of single DNA and PNA strands to an eGFP‐binding nanobody. We show binding of the conjugate to recombinant eGFP and subsequent sequence‐specific annealing of fluorescently labelled imager strands. Furthermore, we reversibly stain eGFP‐tagged proteins in human cells, thus demonstrating the suitability of our conjugation strategy to generate antibody‐oligonucleotides for reversible immunofluorescence imaging. |
format | Online Article Text |
id | pubmed-8048457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80484572021-04-16 Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy Schwach, Jonathan Kolobynina, Ksenia Brandstetter, Katharina Gerlach, Marcus Ochtrop, Philipp Helma, Jonas Hackenberger, Christian P. R. Harz, Hartmann Cardoso, M. Cristina Leonhardt, Heinrich Stengl, Andreas Chembiochem Communications Antibody conjugates have taken a great leap forward as tools in basic and applied molecular life sciences that was enabled by the development of chemoselective reactions for the site‐specific modification of proteins. Antibody‐oligonucleotide conjugates combine the antibody's target specificity with the reversible, sequence‐encoded binding properties of oligonucleotides like DNAs or peptide nucleic acids (PNAs), allowing sequential imaging of large numbers of targets in a single specimen. In this report, we use the Tub‐tag® technology in combination with Cu‐catalyzed azide‐alkyne cycloaddition for the site‐specific conjugation of single DNA and PNA strands to an eGFP‐binding nanobody. We show binding of the conjugate to recombinant eGFP and subsequent sequence‐specific annealing of fluorescently labelled imager strands. Furthermore, we reversibly stain eGFP‐tagged proteins in human cells, thus demonstrating the suitability of our conjugation strategy to generate antibody‐oligonucleotides for reversible immunofluorescence imaging. John Wiley and Sons Inc. 2020-12-17 2021-04-06 /pmc/articles/PMC8048457/ /pubmed/33207032 http://dx.doi.org/10.1002/cbic.202000727 Text en © 2020 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Schwach, Jonathan Kolobynina, Ksenia Brandstetter, Katharina Gerlach, Marcus Ochtrop, Philipp Helma, Jonas Hackenberger, Christian P. R. Harz, Hartmann Cardoso, M. Cristina Leonhardt, Heinrich Stengl, Andreas Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy |
title | Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy |
title_full | Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy |
title_fullStr | Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy |
title_full_unstemmed | Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy |
title_short | Site‐Specific Antibody Fragment Conjugates for Reversible Staining in Fluorescence Microscopy |
title_sort | site‐specific antibody fragment conjugates for reversible staining in fluorescence microscopy |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048457/ https://www.ncbi.nlm.nih.gov/pubmed/33207032 http://dx.doi.org/10.1002/cbic.202000727 |
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