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CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells

CRISPR-Cas9 genome engineering can be used to functionally investigate the complex mechanisms of immune system regulation. Decades of work have aimed to genetically reprogram innate immunity, but current approaches are inefficient or nonspecific, limiting their use. Here, we detail an optimized stra...

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Detalles Bibliográficos
Autores principales: Hildreth, Andrew D., Riggan, Luke, O’Sullivan, Timothy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756923/
https://www.ncbi.nlm.nih.gov/pubmed/33377009
http://dx.doi.org/10.1016/j.xpro.2020.100113
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author Hildreth, Andrew D.
Riggan, Luke
O’Sullivan, Timothy E.
author_facet Hildreth, Andrew D.
Riggan, Luke
O’Sullivan, Timothy E.
author_sort Hildreth, Andrew D.
collection PubMed
description CRISPR-Cas9 genome engineering can be used to functionally investigate the complex mechanisms of immune system regulation. Decades of work have aimed to genetically reprogram innate immunity, but current approaches are inefficient or nonspecific, limiting their use. Here, we detail an optimized strategy for non-viral CRISPR-Cas9 ribonucleoprotein (cRNP) genomic editing of primary innate lymphocytes (ILCs) and myeloid lineage cells, resulting in high-efficiency editing of target gene expression from a single electroporation. For complete details on the use and execution of this protocol, please refer to Riggan et al. (2020).
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spelling pubmed-77569232020-12-28 CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells Hildreth, Andrew D. Riggan, Luke O’Sullivan, Timothy E. STAR Protoc Protocol CRISPR-Cas9 genome engineering can be used to functionally investigate the complex mechanisms of immune system regulation. Decades of work have aimed to genetically reprogram innate immunity, but current approaches are inefficient or nonspecific, limiting their use. Here, we detail an optimized strategy for non-viral CRISPR-Cas9 ribonucleoprotein (cRNP) genomic editing of primary innate lymphocytes (ILCs) and myeloid lineage cells, resulting in high-efficiency editing of target gene expression from a single electroporation. For complete details on the use and execution of this protocol, please refer to Riggan et al. (2020). Elsevier 2020-09-15 /pmc/articles/PMC7756923/ /pubmed/33377009 http://dx.doi.org/10.1016/j.xpro.2020.100113 Text en © 2020 The Author(s) http://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
Hildreth, Andrew D.
Riggan, Luke
O’Sullivan, Timothy E.
CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells
title CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells
title_full CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells
title_fullStr CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells
title_full_unstemmed CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells
title_short CRISPR-Cas9 Ribonucleoprotein-Mediated Genomic Editing in Primary Innate Immune Cells
title_sort crispr-cas9 ribonucleoprotein-mediated genomic editing in primary innate immune cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756923/
https://www.ncbi.nlm.nih.gov/pubmed/33377009
http://dx.doi.org/10.1016/j.xpro.2020.100113
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