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Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide
Lifeact is a 17-residue peptide that can be employed in cell microscopy as a probe for F-actin when fused to fluorescent proteins, but therefore is not suitable for all cell types. We have conjugated fluorescently labelled Lifeact to three different cell-penetrating systems (a myristoylated carrier...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524417/ https://www.ncbi.nlm.nih.gov/pubmed/26062886 http://dx.doi.org/10.1002/cbic.201500120 |
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author | Cardo, Lucia Thomas, Steve G Mazharian, Alexandra Pikramenou, Zoe Rappoport, Joshua Z Hannon, Michael J Watson, Stephen P |
author_facet | Cardo, Lucia Thomas, Steve G Mazharian, Alexandra Pikramenou, Zoe Rappoport, Joshua Z Hannon, Michael J Watson, Stephen P |
author_sort | Cardo, Lucia |
collection | PubMed |
description | Lifeact is a 17-residue peptide that can be employed in cell microscopy as a probe for F-actin when fused to fluorescent proteins, but therefore is not suitable for all cell types. We have conjugated fluorescently labelled Lifeact to three different cell-penetrating systems (a myristoylated carrier (myr), the pH low insertion peptide (pHLIP) and the cationic peptide TAT) as a strategy to deliver Lifeact into cells and developed new tools for actin staining with improved synthetic accessibility and low toxicity, focusing on their suitability in platelets and megakaryocytes. Using confocal microscopy, we characterised the cell distribution of the new hybrids in fixed cells, and found that both myr– and pHLIP–Lifeact conjugates provide efficient actin staining upon cleavage of Lifeact from the carriers, without affecting cell spreading. This new approach could facilitate the design of new tools for actin visualisation. |
format | Online Article Text |
id | pubmed-4524417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-45244172015-08-12 Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide Cardo, Lucia Thomas, Steve G Mazharian, Alexandra Pikramenou, Zoe Rappoport, Joshua Z Hannon, Michael J Watson, Stephen P Chembiochem Full Papers Lifeact is a 17-residue peptide that can be employed in cell microscopy as a probe for F-actin when fused to fluorescent proteins, but therefore is not suitable for all cell types. We have conjugated fluorescently labelled Lifeact to three different cell-penetrating systems (a myristoylated carrier (myr), the pH low insertion peptide (pHLIP) and the cationic peptide TAT) as a strategy to deliver Lifeact into cells and developed new tools for actin staining with improved synthetic accessibility and low toxicity, focusing on their suitability in platelets and megakaryocytes. Using confocal microscopy, we characterised the cell distribution of the new hybrids in fixed cells, and found that both myr– and pHLIP–Lifeact conjugates provide efficient actin staining upon cleavage of Lifeact from the carriers, without affecting cell spreading. This new approach could facilitate the design of new tools for actin visualisation. WILEY-VCH Verlag 2015-07-27 2015-06-15 /pmc/articles/PMC4524417/ /pubmed/26062886 http://dx.doi.org/10.1002/cbic.201500120 Text en © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. https://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Cardo, Lucia Thomas, Steve G Mazharian, Alexandra Pikramenou, Zoe Rappoport, Joshua Z Hannon, Michael J Watson, Stephen P Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide |
title | Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide |
title_full | Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide |
title_fullStr | Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide |
title_full_unstemmed | Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide |
title_short | Accessible Synthetic Probes for Staining Actin inside Platelets and Megakaryocytes by Employing Lifeact Peptide |
title_sort | accessible synthetic probes for staining actin inside platelets and megakaryocytes by employing lifeact peptide |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524417/ https://www.ncbi.nlm.nih.gov/pubmed/26062886 http://dx.doi.org/10.1002/cbic.201500120 |
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