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Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems

Microscopy-based analysis of protein accumulation at a given subcellular location in real time provides invaluable insights into the function of a protein in a specific process. Here, we describe a detailed protocol for determining protein accumulation kinetics at the division site in the budding ye...

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Detalles Bibliográficos
Autores principales: Okada, Hiroki, MacTaggart, Brittany, Bi, Erfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379524/
https://www.ncbi.nlm.nih.gov/pubmed/34458867
http://dx.doi.org/10.1016/j.xpro.2021.100733
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author Okada, Hiroki
MacTaggart, Brittany
Bi, Erfei
author_facet Okada, Hiroki
MacTaggart, Brittany
Bi, Erfei
author_sort Okada, Hiroki
collection PubMed
description Microscopy-based analysis of protein accumulation at a given subcellular location in real time provides invaluable insights into the function of a protein in a specific process. Here, we describe a detailed protocol for determining protein accumulation kinetics at the division site in the budding yeast Saccharomyces cerevisiae and fission yeast Schizosaccharomyces pombe. This protocol can be adapted for the analysis of any protein involved in any process as long as the protein is localized to a discrete region of the cell. For complete details on the use and execution of this protocol, please refer to Okada et al. (2021) and Okada et al. (2019).
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spelling pubmed-83795242021-08-27 Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems Okada, Hiroki MacTaggart, Brittany Bi, Erfei STAR Protoc Protocol Microscopy-based analysis of protein accumulation at a given subcellular location in real time provides invaluable insights into the function of a protein in a specific process. Here, we describe a detailed protocol for determining protein accumulation kinetics at the division site in the budding yeast Saccharomyces cerevisiae and fission yeast Schizosaccharomyces pombe. This protocol can be adapted for the analysis of any protein involved in any process as long as the protein is localized to a discrete region of the cell. For complete details on the use and execution of this protocol, please refer to Okada et al. (2021) and Okada et al. (2019). Elsevier 2021-08-17 /pmc/articles/PMC8379524/ /pubmed/34458867 http://dx.doi.org/10.1016/j.xpro.2021.100733 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Okada, Hiroki
MacTaggart, Brittany
Bi, Erfei
Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
title Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
title_full Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
title_fullStr Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
title_full_unstemmed Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
title_short Analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
title_sort analysis of local protein accumulation kinetics by live-cell imaging in yeast systems
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379524/
https://www.ncbi.nlm.nih.gov/pubmed/34458867
http://dx.doi.org/10.1016/j.xpro.2021.100733
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