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Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells

This protocol describes how to image fluorescently tagged proteins, RNA, or DNA inside living Saccharomyces cerevisiae cells at the single-molecule level. Imaging inside living cells, as opposed to fixed materials, gives access to real-time kinetic information. Although various single-molecule imagi...

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Detalles Bibliográficos
Autores principales: Brouwer, Ineke, Patel, Heta Piyush, Meeussen, Joseph Victor Willem, Pomp, Wim, Lenstra, Tineke Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757289/
https://www.ncbi.nlm.nih.gov/pubmed/33377036
http://dx.doi.org/10.1016/j.xpro.2020.100142
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author Brouwer, Ineke
Patel, Heta Piyush
Meeussen, Joseph Victor Willem
Pomp, Wim
Lenstra, Tineke Laura
author_facet Brouwer, Ineke
Patel, Heta Piyush
Meeussen, Joseph Victor Willem
Pomp, Wim
Lenstra, Tineke Laura
author_sort Brouwer, Ineke
collection PubMed
description This protocol describes how to image fluorescently tagged proteins, RNA, or DNA inside living Saccharomyces cerevisiae cells at the single-molecule level. Imaging inside living cells, as opposed to fixed materials, gives access to real-time kinetic information. Although various single-molecule imaging applications are discussed, we focus on imaging of gene transcription at the single-RNA level. To obtain the best possible results, it is important that both imaging parameters and yeast culture conditions are optimized. Here, both aspects are described. For complete details on the use and execution of this protocol, please refer to Lenstra et al. (2015) and Donovan et al. (2019).
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spelling pubmed-77572892020-12-28 Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells Brouwer, Ineke Patel, Heta Piyush Meeussen, Joseph Victor Willem Pomp, Wim Lenstra, Tineke Laura STAR Protoc Protocol This protocol describes how to image fluorescently tagged proteins, RNA, or DNA inside living Saccharomyces cerevisiae cells at the single-molecule level. Imaging inside living cells, as opposed to fixed materials, gives access to real-time kinetic information. Although various single-molecule imaging applications are discussed, we focus on imaging of gene transcription at the single-RNA level. To obtain the best possible results, it is important that both imaging parameters and yeast culture conditions are optimized. Here, both aspects are described. For complete details on the use and execution of this protocol, please refer to Lenstra et al. (2015) and Donovan et al. (2019). Elsevier 2020-10-17 /pmc/articles/PMC7757289/ /pubmed/33377036 http://dx.doi.org/10.1016/j.xpro.2020.100142 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Brouwer, Ineke
Patel, Heta Piyush
Meeussen, Joseph Victor Willem
Pomp, Wim
Lenstra, Tineke Laura
Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells
title Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells
title_full Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells
title_fullStr Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells
title_full_unstemmed Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells
title_short Single-Molecule Fluorescence Imaging in Living Saccharomyces cerevisiae Cells
title_sort single-molecule fluorescence imaging in living saccharomyces cerevisiae cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757289/
https://www.ncbi.nlm.nih.gov/pubmed/33377036
http://dx.doi.org/10.1016/j.xpro.2020.100142
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