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Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues
Talin is a cell adhesion molecule that is indispensable for the development and function of multicellular organisms. Despite its central role for many cell biological processes, suitable methods to investigate the nanoscale organization of talin in its native environment are missing. Here, we overco...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518977/ https://www.ncbi.nlm.nih.gov/pubmed/34286903 http://dx.doi.org/10.1002/cbic.202100301 |
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author | Fischer, Lisa S. Schlichthaerle, Thomas Chrostek‐Grashoff, Anna Grashoff, Carsten |
author_facet | Fischer, Lisa S. Schlichthaerle, Thomas Chrostek‐Grashoff, Anna Grashoff, Carsten |
author_sort | Fischer, Lisa S. |
collection | PubMed |
description | Talin is a cell adhesion molecule that is indispensable for the development and function of multicellular organisms. Despite its central role for many cell biological processes, suitable methods to investigate the nanoscale organization of talin in its native environment are missing. Here, we overcome this limitation by combining single‐molecule resolved PAINT (points accumulation in nanoscale topography) imaging with the IRIS (image reconstruction by integrating exchangeable single‐molecule localization) approach, enabling the quantitative analysis of genetically unmodified talin molecules in cells. We demonstrate that a previously reported peptide can be utilized to specifically label the two major talin isoforms expressed in mammalian tissues with a localization precision of <10 nm. Our experiments show that the methodology performs equally well as state‐of‐the‐art single‐molecule localization techniques, and the first applications reveal a thus far undescribed cell adhesion structure in differentiating stem cells. Furthermore, we demonstrate the applicability of this peptide‐PAINT technique to mouse tissues paving the way to single‐protein imaging of endogenous talin proteins under physiologically relevant conditions. |
format | Online Article Text |
id | pubmed-8518977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85189772021-10-21 Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues Fischer, Lisa S. Schlichthaerle, Thomas Chrostek‐Grashoff, Anna Grashoff, Carsten Chembiochem Full Papers Talin is a cell adhesion molecule that is indispensable for the development and function of multicellular organisms. Despite its central role for many cell biological processes, suitable methods to investigate the nanoscale organization of talin in its native environment are missing. Here, we overcome this limitation by combining single‐molecule resolved PAINT (points accumulation in nanoscale topography) imaging with the IRIS (image reconstruction by integrating exchangeable single‐molecule localization) approach, enabling the quantitative analysis of genetically unmodified talin molecules in cells. We demonstrate that a previously reported peptide can be utilized to specifically label the two major talin isoforms expressed in mammalian tissues with a localization precision of <10 nm. Our experiments show that the methodology performs equally well as state‐of‐the‐art single‐molecule localization techniques, and the first applications reveal a thus far undescribed cell adhesion structure in differentiating stem cells. Furthermore, we demonstrate the applicability of this peptide‐PAINT technique to mouse tissues paving the way to single‐protein imaging of endogenous talin proteins under physiologically relevant conditions. John Wiley and Sons Inc. 2021-07-30 2021-10-01 /pmc/articles/PMC8518977/ /pubmed/34286903 http://dx.doi.org/10.1002/cbic.202100301 Text en © 2021 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Fischer, Lisa S. Schlichthaerle, Thomas Chrostek‐Grashoff, Anna Grashoff, Carsten Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues |
title | Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues |
title_full | Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues |
title_fullStr | Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues |
title_full_unstemmed | Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues |
title_short | Peptide‐PAINT Enables Investigation of Endogenous Talin with Molecular Scale Resolution in Cells and Tissues |
title_sort | peptide‐paint enables investigation of endogenous talin with molecular scale resolution in cells and tissues |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518977/ https://www.ncbi.nlm.nih.gov/pubmed/34286903 http://dx.doi.org/10.1002/cbic.202100301 |
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