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Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a

We recently developed a system to create human chimeric antigen receptor (CAR)-T cells using conjugated Cas12a (cCas12a) in which Cas12a is covalently linked to its CRISPR RNA (crRNA). This protocol describes site-specific modification of Cas12a and the preparation of Cas12a-crRNA complex using bio-...

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Autores principales: Ling, Xinyu, Chang, Liying, Chen, Heqi, Liu, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038777/
https://www.ncbi.nlm.nih.gov/pubmed/35496795
http://dx.doi.org/10.1016/j.xpro.2022.101321
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author Ling, Xinyu
Chang, Liying
Chen, Heqi
Liu, Tao
author_facet Ling, Xinyu
Chang, Liying
Chen, Heqi
Liu, Tao
author_sort Ling, Xinyu
collection PubMed
description We recently developed a system to create human chimeric antigen receptor (CAR)-T cells using conjugated Cas12a (cCas12a) in which Cas12a is covalently linked to its CRISPR RNA (crRNA). This protocol describes site-specific modification of Cas12a and the preparation of Cas12a-crRNA complex using bio-orthogonal chemistry, followed by CAR-T cell generation through electroporation and AAV infection. This system shows robust editing efficiency in human cells and can be used for precisely targeted, highly efficient integration of CAR genes into T cell genome. For complete details on the use and execution of this protocol, please refer to Ling et al. (2021).
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spelling pubmed-90387772022-04-27 Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a Ling, Xinyu Chang, Liying Chen, Heqi Liu, Tao STAR Protoc Protocol We recently developed a system to create human chimeric antigen receptor (CAR)-T cells using conjugated Cas12a (cCas12a) in which Cas12a is covalently linked to its CRISPR RNA (crRNA). This protocol describes site-specific modification of Cas12a and the preparation of Cas12a-crRNA complex using bio-orthogonal chemistry, followed by CAR-T cell generation through electroporation and AAV infection. This system shows robust editing efficiency in human cells and can be used for precisely targeted, highly efficient integration of CAR genes into T cell genome. For complete details on the use and execution of this protocol, please refer to Ling et al. (2021). Elsevier 2022-04-14 /pmc/articles/PMC9038777/ /pubmed/35496795 http://dx.doi.org/10.1016/j.xpro.2022.101321 Text en © 2022 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
Ling, Xinyu
Chang, Liying
Chen, Heqi
Liu, Tao
Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a
title Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a
title_full Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a
title_fullStr Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a
title_full_unstemmed Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a
title_short Efficient generation of locus-specific human CAR-T cells with CRISPR/cCas12a
title_sort efficient generation of locus-specific human car-t cells with crispr/ccas12a
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038777/
https://www.ncbi.nlm.nih.gov/pubmed/35496795
http://dx.doi.org/10.1016/j.xpro.2022.101321
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