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Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells

Targeted protein degradation using degrons, such as the mini-Auxin-inducible degron (mAID), has an advantage over genetic silencing/knockout. However, the efficiency of sgRNA, homologous recombination, tedious expansion, and screening single clones makes the process of tagging endogenous proteins lo...

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Detalles Bibliográficos
Autores principales: Adhikari, Bikash, Narain, Ashwin, Wolf, Elmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609061/
https://www.ncbi.nlm.nih.gov/pubmed/34849487
http://dx.doi.org/10.1016/j.xpro.2021.100949
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author Adhikari, Bikash
Narain, Ashwin
Wolf, Elmar
author_facet Adhikari, Bikash
Narain, Ashwin
Wolf, Elmar
author_sort Adhikari, Bikash
collection PubMed
description Targeted protein degradation using degrons, such as the mini-Auxin-inducible degron (mAID), has an advantage over genetic silencing/knockout. However, the efficiency of sgRNA, homologous recombination, tedious expansion, and screening single clones makes the process of tagging endogenous proteins long and laborious. This protocol describes a practical and economical way to obtain AID-tagged endogenous proteins using CRISPR/Cas9-mediated homology-directed repair (HDR). We use the generation of endogenously AID-tagged SPT6 in U2OS cells as an example but provide sufficient details for usage in other cell types. For complete details on the use and execution of this protocol, please refer to Narain et al. (2021).
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spelling pubmed-86090612021-11-29 Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells Adhikari, Bikash Narain, Ashwin Wolf, Elmar STAR Protoc Protocol Targeted protein degradation using degrons, such as the mini-Auxin-inducible degron (mAID), has an advantage over genetic silencing/knockout. However, the efficiency of sgRNA, homologous recombination, tedious expansion, and screening single clones makes the process of tagging endogenous proteins long and laborious. This protocol describes a practical and economical way to obtain AID-tagged endogenous proteins using CRISPR/Cas9-mediated homology-directed repair (HDR). We use the generation of endogenously AID-tagged SPT6 in U2OS cells as an example but provide sufficient details for usage in other cell types. For complete details on the use and execution of this protocol, please refer to Narain et al. (2021). Elsevier 2021-11-19 /pmc/articles/PMC8609061/ /pubmed/34849487 http://dx.doi.org/10.1016/j.xpro.2021.100949 Text en © 2021 The Author(s) 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
Adhikari, Bikash
Narain, Ashwin
Wolf, Elmar
Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells
title Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells
title_full Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells
title_fullStr Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells
title_full_unstemmed Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells
title_short Generation of auxin inducible degron (AID) knock-in cell lines for targeted protein degradation in mammalian cells
title_sort generation of auxin inducible degron (aid) knock-in cell lines for targeted protein degradation in mammalian cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609061/
https://www.ncbi.nlm.nih.gov/pubmed/34849487
http://dx.doi.org/10.1016/j.xpro.2021.100949
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