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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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). |
format | Online Article Text |
id | pubmed-9038778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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