Different Methods of Delivering CRISPR/Cas9 Into Cells
DC Field | Value | Language |
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dc.contributor.author | Chandrasekaran, Arun Pandian | - |
dc.contributor.author | Song, Minjung | - |
dc.contributor.author | Kim, Kye-Seong | - |
dc.contributor.author | Ramakrishna, Suresh | - |
dc.date.accessioned | 2022-07-12T20:02:41Z | - |
dc.date.available | 2022-07-12T20:02:41Z | - |
dc.date.created | 2021-05-11 | - |
dc.date.issued | 2018 | - |
dc.identifier.issn | 1877-1173 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150909 | - |
dc.description.abstract | Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated system (Cas) is comprised of repetitive bases followed by short fragments of DNA from a previously invading organism that provide immunity to the most prokaryotic organisms. An RNA-dependent spacer is required for CRISPR/Cas9 to recognize the target DNA. Delivery of the CRISPR/Cas9-guide RNA (gRNA) complex to any cell results in modification of the target sequence. The CRISPR/Cas9-mediated genome editing technique is currently in the spotlight and has several research interests, including molecular medicine and agriculture. There are several factors that hinder the delivery of this complex, such as the large size of the plasmid or high dosage of the chemical agent. There are several methods available to deliver CRISPR/Cas9 and its components to the target cells. It includes viral, non-viral and physical methods to deliver plasmid or ribonucleoprotein (RNP) of CRISPR components. But in vivo CRISPR/Cas9 delivery remains challenging to the researchers due to insertional mutagenesis, targeted delivery, immunogenicity, and off-targets. However, studies suggesting that the CRISPR/Cas9-RNP delivery can overcome these hurdles. Here, we review the various methods for delivery of CRISPR/Cas9 and gRNA to several cell lines, highlighting the limitations of each approach, and suggest possible alternative methods. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | ELSEVIER ACADEMIC PRESS INC | - |
dc.title | Different Methods of Delivering CRISPR/Cas9 Into Cells | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Kim, Kye-Seong | - |
dc.contributor.affiliatedAuthor | Ramakrishna, Suresh | - |
dc.identifier.doi | 10.1016/bs.pmbts.2018.05.001 | - |
dc.identifier.scopusid | 2-s2.0-85048347140 | - |
dc.identifier.wosid | 000452376200007 | - |
dc.identifier.bibliographicCitation | PROGRESS IN MOLECULAR BIOLOGY AND TRANSLATIONAL SCIENCE, VOL 159, v.159, pp.157 - 176 | - |
dc.relation.isPartOf | PROGRESS IN MOLECULAR BIOLOGY AND TRANSLATIONAL SCIENCE, VOL 159 | - |
dc.citation.title | PROGRESS IN MOLECULAR BIOLOGY AND TRANSLATIONAL SCIENCE, VOL 159 | - |
dc.citation.volume | 159 | - |
dc.citation.startPage | 157 | - |
dc.citation.endPage | 176 | - |
dc.type.rims | ART | - |
dc.type.docType | Review; Book Chapter | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.subject.keywordPlus | HUMAN HEMATOPOIETIC STEM | - |
dc.subject.keywordPlus | GENE-TRANSFER | - |
dc.subject.keywordPlus | LENTIVIRAL VECTORS | - |
dc.subject.keywordPlus | VIRAL VECTORS | - |
dc.subject.keywordPlus | CAS9 PROTEIN | - |
dc.subject.keywordPlus | MOUSE MODEL | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | GENOME | - |
dc.subject.keywordPlus | RNA | - |
dc.subject.keywordPlus | CRISPR-CAS9 | - |
dc.subject.keywordAuthor | Clustered regularly interspaced short palindromic repeats | - |
dc.subject.keywordAuthor | Delivery methods | - |
dc.subject.keywordAuthor | Gene modification | - |
dc.subject.keywordAuthor | Guide RNA | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/abs/pii/S1877117318300796?via%3Dihub | - |
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