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Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing

[Image: see text] CRISPR/Cas9 system is a promising approach for gene editing in gene therapy. Effective gene editing requires safe and efficient delivery of CRISPR/Cas9 system in target cells. Several new multifunctional pH-sensitive amino lipids were designed and synthesized with modification of t...

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Autores principales: Sun, Da, Sun, Zhanhu, Jiang, Hongfa, Vaidya, Amita M., Xin, Rui, Ayat, Nadia R., Schilb, Andrew L., Qiao, Peter L., Han, Zheng, Naderi, Amirreza, Lu, Zheng-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429435/
https://www.ncbi.nlm.nih.gov/pubmed/30582790
http://dx.doi.org/10.1021/acs.bioconjchem.8b00856
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author Sun, Da
Sun, Zhanhu
Jiang, Hongfa
Vaidya, Amita M.
Xin, Rui
Ayat, Nadia R.
Schilb, Andrew L.
Qiao, Peter L.
Han, Zheng
Naderi, Amirreza
Lu, Zheng-Rong
author_facet Sun, Da
Sun, Zhanhu
Jiang, Hongfa
Vaidya, Amita M.
Xin, Rui
Ayat, Nadia R.
Schilb, Andrew L.
Qiao, Peter L.
Han, Zheng
Naderi, Amirreza
Lu, Zheng-Rong
author_sort Sun, Da
collection PubMed
description [Image: see text] CRISPR/Cas9 system is a promising approach for gene editing in gene therapy. Effective gene editing requires safe and efficient delivery of CRISPR/Cas9 system in target cells. Several new multifunctional pH-sensitive amino lipids were designed and synthesized with modification of the amino head groups for intracellular delivery of CRISPR/Cas9 system. These multifunctional pH-sensitive amino lipids exhibited structurally dependent formulation of stable nanoparticles with the DNA plasmids of CRISPR/Cas9 system with the sizes ranging from 100 to 200 nm. The amino lipid plasmid DNA nanoparticles showed pH-sensitive hemolysis with minimal hemolytic activity at pH 7.4 and increased hemolysis at acidic pH (pH = 5.5, 6.5). The nanoparticles exhibited low cytotoxicity at an N/P ratio of 10. Expression of both Cas9 and sgRNA of the CRISPR/Cas9 system was in the range from 4.4% to 33%, dependent on the lipid structure in NIH3T3-GFP cells. The amino lipids that formed stable nanoparticles with high expression of both Cas9 and sgRNA mediated high gene editing efficiency. ECO and iECO mediated more efficient gene editing than other tested lipids. ECO mediated up to 50% GFP suppression based on observations with confocal microscopy and nearly 80% reduction of GFP mRNA based on RT-PCR measurement in NIH3T3-GFP cells. The multifunctional pH-sensitive amino lipids have the potential for efficient intracellular delivery of CRISPR/Cas9 for effective gene editing.
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spelling pubmed-64294352019-03-25 Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing Sun, Da Sun, Zhanhu Jiang, Hongfa Vaidya, Amita M. Xin, Rui Ayat, Nadia R. Schilb, Andrew L. Qiao, Peter L. Han, Zheng Naderi, Amirreza Lu, Zheng-Rong Bioconjug Chem [Image: see text] CRISPR/Cas9 system is a promising approach for gene editing in gene therapy. Effective gene editing requires safe and efficient delivery of CRISPR/Cas9 system in target cells. Several new multifunctional pH-sensitive amino lipids were designed and synthesized with modification of the amino head groups for intracellular delivery of CRISPR/Cas9 system. These multifunctional pH-sensitive amino lipids exhibited structurally dependent formulation of stable nanoparticles with the DNA plasmids of CRISPR/Cas9 system with the sizes ranging from 100 to 200 nm. The amino lipid plasmid DNA nanoparticles showed pH-sensitive hemolysis with minimal hemolytic activity at pH 7.4 and increased hemolysis at acidic pH (pH = 5.5, 6.5). The nanoparticles exhibited low cytotoxicity at an N/P ratio of 10. Expression of both Cas9 and sgRNA of the CRISPR/Cas9 system was in the range from 4.4% to 33%, dependent on the lipid structure in NIH3T3-GFP cells. The amino lipids that formed stable nanoparticles with high expression of both Cas9 and sgRNA mediated high gene editing efficiency. ECO and iECO mediated more efficient gene editing than other tested lipids. ECO mediated up to 50% GFP suppression based on observations with confocal microscopy and nearly 80% reduction of GFP mRNA based on RT-PCR measurement in NIH3T3-GFP cells. The multifunctional pH-sensitive amino lipids have the potential for efficient intracellular delivery of CRISPR/Cas9 for effective gene editing. American Chemical Society 2018-12-24 2019-03-20 /pmc/articles/PMC6429435/ /pubmed/30582790 http://dx.doi.org/10.1021/acs.bioconjchem.8b00856 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Sun, Da
Sun, Zhanhu
Jiang, Hongfa
Vaidya, Amita M.
Xin, Rui
Ayat, Nadia R.
Schilb, Andrew L.
Qiao, Peter L.
Han, Zheng
Naderi, Amirreza
Lu, Zheng-Rong
Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing
title Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing
title_full Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing
title_fullStr Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing
title_full_unstemmed Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing
title_short Synthesis and Evaluation of pH-Sensitive Multifunctional Lipids for Efficient Delivery of CRISPR/Cas9 in Gene Editing
title_sort synthesis and evaluation of ph-sensitive multifunctional lipids for efficient delivery of crispr/cas9 in gene editing
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429435/
https://www.ncbi.nlm.nih.gov/pubmed/30582790
http://dx.doi.org/10.1021/acs.bioconjchem.8b00856
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