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Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates

Bio-imaging is a key technique in tracking and monitoring important biological processes and fundamental biomolecular interactions, however the interference of background autofluorescence with targeted fluorophores is problematic for many bio-imaging applications. This study reports on two novel met...

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Autores principales: Cordina, Nicole M., Sayyadi, Nima, Parker, Lindsay M., Everest-Dass, Arun, Brown, Louise J., Packer, Nicolle H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851999/
https://www.ncbi.nlm.nih.gov/pubmed/29540838
http://dx.doi.org/10.1038/s41598-018-22702-1
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author Cordina, Nicole M.
Sayyadi, Nima
Parker, Lindsay M.
Everest-Dass, Arun
Brown, Louise J.
Packer, Nicolle H.
author_facet Cordina, Nicole M.
Sayyadi, Nima
Parker, Lindsay M.
Everest-Dass, Arun
Brown, Louise J.
Packer, Nicolle H.
author_sort Cordina, Nicole M.
collection PubMed
description Bio-imaging is a key technique in tracking and monitoring important biological processes and fundamental biomolecular interactions, however the interference of background autofluorescence with targeted fluorophores is problematic for many bio-imaging applications. This study reports on two novel methods for reducing interference with cellular autofluorescence for bio-imaging. The first method uses fluorescent nanodiamonds (FNDs), containing nitrogen vacancy centers. FNDs emit at near-infrared wavelengths typically higher than most cellular autofluorescence; and when appropriately functionalized, can be used for background-free imaging of targeted biomolecules. The second method uses europium-chelating tags with long fluorescence lifetimes. These europium-chelating tags enhance background-free imaging due to the short fluorescent lifetimes of cellular autofluorescence. In this study, we used both methods to target E-selectin, a transmembrane glycoprotein that is activated by inflammation, to demonstrate background-free fluorescent staining in fixed endothelial cells. Our findings indicate that both FND and Europium based staining can improve fluorescent bio-imaging capabilities by reducing competition with cellular autofluorescence. 30 nm nanodiamonds coated with the E-selectin antibody was found to enable the most sensitive detective of E-selectin in inflamed cells, with a 40-fold increase in intensity detected.
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spelling pubmed-58519992018-03-21 Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates Cordina, Nicole M. Sayyadi, Nima Parker, Lindsay M. Everest-Dass, Arun Brown, Louise J. Packer, Nicolle H. Sci Rep Article Bio-imaging is a key technique in tracking and monitoring important biological processes and fundamental biomolecular interactions, however the interference of background autofluorescence with targeted fluorophores is problematic for many bio-imaging applications. This study reports on two novel methods for reducing interference with cellular autofluorescence for bio-imaging. The first method uses fluorescent nanodiamonds (FNDs), containing nitrogen vacancy centers. FNDs emit at near-infrared wavelengths typically higher than most cellular autofluorescence; and when appropriately functionalized, can be used for background-free imaging of targeted biomolecules. The second method uses europium-chelating tags with long fluorescence lifetimes. These europium-chelating tags enhance background-free imaging due to the short fluorescent lifetimes of cellular autofluorescence. In this study, we used both methods to target E-selectin, a transmembrane glycoprotein that is activated by inflammation, to demonstrate background-free fluorescent staining in fixed endothelial cells. Our findings indicate that both FND and Europium based staining can improve fluorescent bio-imaging capabilities by reducing competition with cellular autofluorescence. 30 nm nanodiamonds coated with the E-selectin antibody was found to enable the most sensitive detective of E-selectin in inflamed cells, with a 40-fold increase in intensity detected. Nature Publishing Group UK 2018-03-14 /pmc/articles/PMC5851999/ /pubmed/29540838 http://dx.doi.org/10.1038/s41598-018-22702-1 Text en © The Author(s) 2018 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
Cordina, Nicole M.
Sayyadi, Nima
Parker, Lindsay M.
Everest-Dass, Arun
Brown, Louise J.
Packer, Nicolle H.
Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
title Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
title_full Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
title_fullStr Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
title_full_unstemmed Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
title_short Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
title_sort reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851999/
https://www.ncbi.nlm.nih.gov/pubmed/29540838
http://dx.doi.org/10.1038/s41598-018-22702-1
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