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Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast

Chemically induced dimerization (CID) is a useful tool for artificially inducing protein-protein interactions. Although CID has been used extensively for live-cell microscopy applications in mammalian systems, it is rarely utilized in yeast cell biology studies. Here, we present a step-by-step proto...

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Detalles Bibliográficos
Autores principales: Lamb, Andrew K., Di Pietro, Santiago M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038778/
https://www.ncbi.nlm.nih.gov/pubmed/35496798
http://dx.doi.org/10.1016/j.xpro.2022.101323
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author Lamb, Andrew K.
Di Pietro, Santiago M.
author_facet Lamb, Andrew K.
Di Pietro, Santiago M.
author_sort Lamb, Andrew K.
collection PubMed
description Chemically induced dimerization (CID) is a useful tool for artificially inducing protein-protein interactions. Although CID has been used extensively for live-cell microscopy applications in mammalian systems, it is rarely utilized in yeast cell biology studies. Here, we present a step-by-step protocol for the utilization of a CID system in live-cell microscopy experiments of budding yeast endocytosis. While focusing on the study of endocytosis, this protocol framework is adaptable to the study of other cellular processes in Saccharomyces cerevisiae. For complete details on the use and execution of this protocol, please refer to Lamb et al. (2021).
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spelling pubmed-90387782022-04-27 Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast Lamb, Andrew K. Di Pietro, Santiago M. STAR Protoc Protocol Chemically induced dimerization (CID) is a useful tool for artificially inducing protein-protein interactions. Although CID has been used extensively for live-cell microscopy applications in mammalian systems, it is rarely utilized in yeast cell biology studies. Here, we present a step-by-step protocol for the utilization of a CID system in live-cell microscopy experiments of budding yeast endocytosis. While focusing on the study of endocytosis, this protocol framework is adaptable to the study of other cellular processes in Saccharomyces cerevisiae. For complete details on the use and execution of this protocol, please refer to Lamb et al. (2021). Elsevier 2022-04-14 /pmc/articles/PMC9038778/ /pubmed/35496798 http://dx.doi.org/10.1016/j.xpro.2022.101323 Text en © 2022 The Authors 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
Lamb, Andrew K.
Di Pietro, Santiago M.
Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast
title Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast
title_full Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast
title_fullStr Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast
title_full_unstemmed Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast
title_short Utilizing chemically induced dimerization of FKBP to analyze endocytosis by live-cell imaging in budding yeast
title_sort utilizing chemically induced dimerization of fkbp to analyze endocytosis by live-cell imaging in budding yeast
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038778/
https://www.ncbi.nlm.nih.gov/pubmed/35496798
http://dx.doi.org/10.1016/j.xpro.2022.101323
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