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Suitable transfection methods for single particle tracing in plant suspension cells
BACKGROUND: A multitude of different imaging systems are already available to image genetically altered RNA species; however, only a few of these techniques are actually suitable to visualize endogenous RNA. One possibility is to use fluorescently-labelled and hybridization-sensitive probes. In orde...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076440/ https://www.ncbi.nlm.nih.gov/pubmed/24991230 http://dx.doi.org/10.1186/1746-4811-10-15 |
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author | Göhring, Janett Fulcher, Nick Schilcher, Kurt Barta, Andrea Jacak, Jaroslaw |
author_facet | Göhring, Janett Fulcher, Nick Schilcher, Kurt Barta, Andrea Jacak, Jaroslaw |
author_sort | Göhring, Janett |
collection | PubMed |
description | BACKGROUND: A multitude of different imaging systems are already available to image genetically altered RNA species; however, only a few of these techniques are actually suitable to visualize endogenous RNA. One possibility is to use fluorescently-labelled and hybridization-sensitive probes. In order to yield more information about the exact localization and movement of a single RNA molecule, it is necessary to image such probes with highly sensitive microscope setups. More challenges arise if such experiments are conducted in plant cells due to their high autofluorescence and demanding transfection procedures. RESULTS: Here, we report in planta imaging of single RNA molecules using fluorescently labeled molecular beacons. We tested three different transfection protocols in order to identify optimal conditions for transfection of fluorescent DNA probes and their subsequent detection at the single molecule level. CONCLUSIONS: We found that an optimized heat shock protocol provided a vastly improved transfection method for small DNA molecules which were used for subsequent single RNA molecule detection in living plant suspension cells. |
format | Online Article Text |
id | pubmed-4076440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40764402014-07-02 Suitable transfection methods for single particle tracing in plant suspension cells Göhring, Janett Fulcher, Nick Schilcher, Kurt Barta, Andrea Jacak, Jaroslaw Plant Methods Methodology BACKGROUND: A multitude of different imaging systems are already available to image genetically altered RNA species; however, only a few of these techniques are actually suitable to visualize endogenous RNA. One possibility is to use fluorescently-labelled and hybridization-sensitive probes. In order to yield more information about the exact localization and movement of a single RNA molecule, it is necessary to image such probes with highly sensitive microscope setups. More challenges arise if such experiments are conducted in plant cells due to their high autofluorescence and demanding transfection procedures. RESULTS: Here, we report in planta imaging of single RNA molecules using fluorescently labeled molecular beacons. We tested three different transfection protocols in order to identify optimal conditions for transfection of fluorescent DNA probes and their subsequent detection at the single molecule level. CONCLUSIONS: We found that an optimized heat shock protocol provided a vastly improved transfection method for small DNA molecules which were used for subsequent single RNA molecule detection in living plant suspension cells. BioMed Central 2014-05-31 /pmc/articles/PMC4076440/ /pubmed/24991230 http://dx.doi.org/10.1186/1746-4811-10-15 Text en Copyright © 2014 Göhring et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Göhring, Janett Fulcher, Nick Schilcher, Kurt Barta, Andrea Jacak, Jaroslaw Suitable transfection methods for single particle tracing in plant suspension cells |
title | Suitable transfection methods for single particle tracing in plant suspension cells |
title_full | Suitable transfection methods for single particle tracing in plant suspension cells |
title_fullStr | Suitable transfection methods for single particle tracing in plant suspension cells |
title_full_unstemmed | Suitable transfection methods for single particle tracing in plant suspension cells |
title_short | Suitable transfection methods for single particle tracing in plant suspension cells |
title_sort | suitable transfection methods for single particle tracing in plant suspension cells |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076440/ https://www.ncbi.nlm.nih.gov/pubmed/24991230 http://dx.doi.org/10.1186/1746-4811-10-15 |
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