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Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes

Here, we present a protocol combining co-immunoprecipitation (Co-IP) and immunofluorescence approaches with cell cycle stage synchronization to detect cell-cycle-specific complexes. We describe steps to synchronize cells at specific cell cycle stages using drugs. We then detail the preparation of ce...

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Detalles Bibliográficos
Autores principales: Habu, Toshiyuki, Kim, Jiyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881401/
https://www.ncbi.nlm.nih.gov/pubmed/36853678
http://dx.doi.org/10.1016/j.xpro.2023.102063
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author Habu, Toshiyuki
Kim, Jiyeong
author_facet Habu, Toshiyuki
Kim, Jiyeong
author_sort Habu, Toshiyuki
collection PubMed
description Here, we present a protocol combining co-immunoprecipitation (Co-IP) and immunofluorescence approaches with cell cycle stage synchronization to detect cell-cycle-specific complexes. We describe steps to synchronize cells at specific cell cycle stages using drugs. We then detail the preparation of cell extracts from synchronized cells and fractionation of the protein complexes with density centrifugation, followed by Co-IP with specific antibodies. Protein-protein interactions are confirmed by localization using immunofluorescence imaging. This protocol is helpful for visualizing the dynamics of protein complex assembly. For complete details on the use and execution of this protocol, please refer to Habu and Kim (2021).(1)
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spelling pubmed-98814012023-01-28 Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes Habu, Toshiyuki Kim, Jiyeong STAR Protoc Protocol Here, we present a protocol combining co-immunoprecipitation (Co-IP) and immunofluorescence approaches with cell cycle stage synchronization to detect cell-cycle-specific complexes. We describe steps to synchronize cells at specific cell cycle stages using drugs. We then detail the preparation of cell extracts from synchronized cells and fractionation of the protein complexes with density centrifugation, followed by Co-IP with specific antibodies. Protein-protein interactions are confirmed by localization using immunofluorescence imaging. This protocol is helpful for visualizing the dynamics of protein complex assembly. For complete details on the use and execution of this protocol, please refer to Habu and Kim (2021).(1) Elsevier 2023-01-24 /pmc/articles/PMC9881401/ /pubmed/36853678 http://dx.doi.org/10.1016/j.xpro.2023.102063 Text en © 2023 The Authors https://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
Habu, Toshiyuki
Kim, Jiyeong
Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
title Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
title_full Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
title_fullStr Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
title_full_unstemmed Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
title_short Protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
title_sort protocol for combining immunological procedures with cell cycle stage synchronization to detect cell-cycle-specific complexes
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881401/
https://www.ncbi.nlm.nih.gov/pubmed/36853678
http://dx.doi.org/10.1016/j.xpro.2023.102063
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