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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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). |
format | Online Article Text |
id | pubmed-8609061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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