Genome Editing in a Wide Area of the Brain Using Dendrimer-Based Ternary Polyplexes of Cas9 Ribonucleoprotein
A preassembled Cas9/single-guide RNA complex (Cas9 ribonucleoprotein; Cas9 RNP) induces genome editing efficiently, with small off-target effects compared with the conventional techniques, such as plasmid DNA and mRNA systems. However, penetration of Cas9 RNP through the cell membrane is low. In par...
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Veröffentlicht in: | ACS applied materials & interfaces 2020-05, Vol.12 (19), p.21386-21397 |
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creator | Taharabaru, Toru Yokoyama, Ryoma Higashi, Taishi Mohammed, Ahmed Fouad Abdelwahab Inoue, Masamichi Maeda, Yuki Niidome, Takuro Onodera, Risako Motoyama, Keiichi |
description | A preassembled Cas9/single-guide RNA complex (Cas9 ribonucleoprotein; Cas9 RNP) induces genome editing efficiently, with small off-target effects compared with the conventional techniques, such as plasmid DNA and mRNA systems. However, penetration of Cas9 RNP through the cell membrane is low. In particular, the incorporation of Cas9 RNP into neurons and the brain is challenging. In the present study, we have reported the use of a dendrimer (generation 3; G3)/glucuronylglucosyl-β-cyclodextrin conjugate (GUG-β-CDE (G3)) as a carrier of Cas9 RNP and evaluated genome editing activity in the neuron and the brain. A Cas9 RNP ternary complex with GUG-β-CDE (G3) was prepared by only mixing the components. The resulting complex exhibited higher genome editing activity than the complex with the dendrimer (G3), Lipofectamine 3000 or Lipofectamine CRISPRMAX in SH-SY5Y cells, a human neuroblastoma cell line. In addition, GUG-β-CDE (G3) enhanced the genome editing activity of Cas9 RNP in the whole mouse brain after a single intraventricular administration. Thus, GUG-β-CDE (G3) is a useful Cas9 RNP carrier that can induce genome editing in the neuron and brain. |
doi_str_mv | 10.1021/acsami.9b21667 |
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However, penetration of Cas9 RNP through the cell membrane is low. In particular, the incorporation of Cas9 RNP into neurons and the brain is challenging. In the present study, we have reported the use of a dendrimer (generation 3; G3)/glucuronylglucosyl-β-cyclodextrin conjugate (GUG-β-CDE (G3)) as a carrier of Cas9 RNP and evaluated genome editing activity in the neuron and the brain. A Cas9 RNP ternary complex with GUG-β-CDE (G3) was prepared by only mixing the components. The resulting complex exhibited higher genome editing activity than the complex with the dendrimer (G3), Lipofectamine 3000 or Lipofectamine CRISPRMAX in SH-SY5Y cells, a human neuroblastoma cell line. In addition, GUG-β-CDE (G3) enhanced the genome editing activity of Cas9 RNP in the whole mouse brain after a single intraventricular administration. 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Mater. Interfaces</addtitle><description>A preassembled Cas9/single-guide RNA complex (Cas9 ribonucleoprotein; Cas9 RNP) induces genome editing efficiently, with small off-target effects compared with the conventional techniques, such as plasmid DNA and mRNA systems. However, penetration of Cas9 RNP through the cell membrane is low. In particular, the incorporation of Cas9 RNP into neurons and the brain is challenging. In the present study, we have reported the use of a dendrimer (generation 3; G3)/glucuronylglucosyl-β-cyclodextrin conjugate (GUG-β-CDE (G3)) as a carrier of Cas9 RNP and evaluated genome editing activity in the neuron and the brain. A Cas9 RNP ternary complex with GUG-β-CDE (G3) was prepared by only mixing the components. The resulting complex exhibited higher genome editing activity than the complex with the dendrimer (G3), Lipofectamine 3000 or Lipofectamine CRISPRMAX in SH-SY5Y cells, a human neuroblastoma cell line. In addition, GUG-β-CDE (G3) enhanced the genome editing activity of Cas9 RNP in the whole mouse brain after a single intraventricular administration. Thus, GUG-β-CDE (G3) is a useful Cas9 RNP carrier that can induce genome editing in the neuron and brain.</description><subject>Animals</subject><subject>Brain - metabolism</subject><subject>Cell Line, Tumor</subject><subject>CRISPR-Associated Protein 9 - pharmacology</subject><subject>CRISPR-Cas Systems</subject><subject>Dendrimers - chemistry</subject><subject>Drug Carriers - chemistry</subject><subject>Gene Editing - methods</subject><subject>Gene Transfer Techniques</subject><subject>Humans</subject><subject>Mice, Inbred BALB C</subject><subject>Ribonucleoproteins - pharmacology</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1Lw0AQxRdRbK1ePcqehdT9bnLsl1UoKNLiMWySWd2SZMNuCva_NyW1N08zML_3ePMQuqdkTAmjTzoPurLjJGNUqckFGtJEiChmkl2edyEG6CaEHSGKMyKv0YAzTiWVaoiqFdSuArwsbGvrL2xrrPGnLQBPPWjsDG6_Ac-87g7bcCQWUBfeVuCjmQ5Q4A34WvsDfnfloSnhB8JRNdchwR82c_U-L8E13rVg61t0ZXQZ4O40R2j7vNzMX6L12-p1Pl1HmieqjRTkXE7iQiqqDQgjDM1lAYYlmlHItGQkzigkKgZN44TERJhYq5wrwTibMD5C49439y4EDyZtushdypSS9Nhb2veWnnrrBA-9oNlnFRRn_K-oDnjsgU6Y7ty--7kM_7n9Aik-eC8</recordid><startdate>20200513</startdate><enddate>20200513</enddate><creator>Taharabaru, Toru</creator><creator>Yokoyama, Ryoma</creator><creator>Higashi, Taishi</creator><creator>Mohammed, Ahmed Fouad Abdelwahab</creator><creator>Inoue, Masamichi</creator><creator>Maeda, Yuki</creator><creator>Niidome, Takuro</creator><creator>Onodera, Risako</creator><creator>Motoyama, Keiichi</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-8439-5377</orcidid><orcidid>https://orcid.org/0000-0002-8070-8708</orcidid></search><sort><creationdate>20200513</creationdate><title>Genome Editing in a Wide Area of the Brain Using Dendrimer-Based Ternary Polyplexes of Cas9 Ribonucleoprotein</title><author>Taharabaru, Toru ; Yokoyama, Ryoma ; Higashi, Taishi ; Mohammed, Ahmed Fouad Abdelwahab ; Inoue, Masamichi ; Maeda, Yuki ; Niidome, Takuro ; Onodera, Risako ; Motoyama, Keiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a396t-6ec3578d561afe4f4f1c5def29a21eba5208b1e968ea1890804f8a6c364232723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Brain - metabolism</topic><topic>Cell Line, Tumor</topic><topic>CRISPR-Associated Protein 9 - pharmacology</topic><topic>CRISPR-Cas Systems</topic><topic>Dendrimers - chemistry</topic><topic>Drug Carriers - chemistry</topic><topic>Gene Editing - methods</topic><topic>Gene Transfer Techniques</topic><topic>Humans</topic><topic>Mice, Inbred BALB C</topic><topic>Ribonucleoproteins - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Taharabaru, Toru</creatorcontrib><creatorcontrib>Yokoyama, Ryoma</creatorcontrib><creatorcontrib>Higashi, Taishi</creatorcontrib><creatorcontrib>Mohammed, Ahmed Fouad Abdelwahab</creatorcontrib><creatorcontrib>Inoue, Masamichi</creatorcontrib><creatorcontrib>Maeda, Yuki</creatorcontrib><creatorcontrib>Niidome, Takuro</creatorcontrib><creatorcontrib>Onodera, Risako</creatorcontrib><creatorcontrib>Motoyama, Keiichi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Taharabaru, Toru</au><au>Yokoyama, Ryoma</au><au>Higashi, Taishi</au><au>Mohammed, Ahmed Fouad Abdelwahab</au><au>Inoue, Masamichi</au><au>Maeda, Yuki</au><au>Niidome, Takuro</au><au>Onodera, Risako</au><au>Motoyama, Keiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome Editing in a Wide Area of the Brain Using Dendrimer-Based Ternary Polyplexes of Cas9 Ribonucleoprotein</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2020-05-13</date><risdate>2020</risdate><volume>12</volume><issue>19</issue><spage>21386</spage><epage>21397</epage><pages>21386-21397</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>A preassembled Cas9/single-guide RNA complex (Cas9 ribonucleoprotein; Cas9 RNP) induces genome editing efficiently, with small off-target effects compared with the conventional techniques, such as plasmid DNA and mRNA systems. However, penetration of Cas9 RNP through the cell membrane is low. In particular, the incorporation of Cas9 RNP into neurons and the brain is challenging. In the present study, we have reported the use of a dendrimer (generation 3; G3)/glucuronylglucosyl-β-cyclodextrin conjugate (GUG-β-CDE (G3)) as a carrier of Cas9 RNP and evaluated genome editing activity in the neuron and the brain. A Cas9 RNP ternary complex with GUG-β-CDE (G3) was prepared by only mixing the components. The resulting complex exhibited higher genome editing activity than the complex with the dendrimer (G3), Lipofectamine 3000 or Lipofectamine CRISPRMAX in SH-SY5Y cells, a human neuroblastoma cell line. In addition, GUG-β-CDE (G3) enhanced the genome editing activity of Cas9 RNP in the whole mouse brain after a single intraventricular administration. Thus, GUG-β-CDE (G3) is a useful Cas9 RNP carrier that can induce genome editing in the neuron and brain.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>32315156</pmid><doi>10.1021/acsami.9b21667</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8439-5377</orcidid><orcidid>https://orcid.org/0000-0002-8070-8708</orcidid></addata></record> |
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subjects | Animals Brain - metabolism Cell Line, Tumor CRISPR-Associated Protein 9 - pharmacology CRISPR-Cas Systems Dendrimers - chemistry Drug Carriers - chemistry Gene Editing - methods Gene Transfer Techniques Humans Mice, Inbred BALB C Ribonucleoproteins - pharmacology |
title | Genome Editing in a Wide Area of the Brain Using Dendrimer-Based Ternary Polyplexes of Cas9 Ribonucleoprotein |
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