Standard

Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing. / Amirkhanov, R. N.; Stepanov, G. A.

в: Russian Journal of Bioorganic Chemistry, Том 45, № 6, 01.11.2019, стр. 431-437.

Результаты исследований: Научные публикации в периодических изданияхобзорная статьяРецензирование

Harvard

Amirkhanov, RN & Stepanov, GA 2019, 'Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing', Russian Journal of Bioorganic Chemistry, Том. 45, № 6, стр. 431-437. https://doi.org/10.1134/S1068162019060025

APA

Amirkhanov, R. N., & Stepanov, G. A. (2019). Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing. Russian Journal of Bioorganic Chemistry, 45(6), 431-437. https://doi.org/10.1134/S1068162019060025

Vancouver

Amirkhanov RN, Stepanov GA. Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing. Russian Journal of Bioorganic Chemistry. 2019 нояб. 1;45(6):431-437. doi: 10.1134/S1068162019060025

Author

Amirkhanov, R. N. ; Stepanov, G. A. / Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing. в: Russian Journal of Bioorganic Chemistry. 2019 ; Том 45, № 6. стр. 431-437.

BibTeX

@article{66d46134083c4a318a0cc7121a3f9370,
title = "Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing",
abstract = "The discovery of RNA-guided nucleases have enabled to leap forward in genome editing of cells and organisms. These nucleases can be delivered into cells as plasmid DNA, mRNA or ribonucleoprotein complexes (RNPs). The delivery in the form of RNP has some advantages because the target gene editing begins immediately without the process of intracellular synthesis of components and CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9 (CRISPR associated protein 9) system assembly. This strategy makes it possible to directly control RNP concentration and to decrease the number of off-targets due to rapid degradation of the complex in the cell. However, the task to develop RNP delivery systems remains unsolved. This review is devoted to RNP delivery into cells and tissues using physical approaches and different carriers. Special attention is paid to novel approaches that improve the RNP delivery efficiency.",
keywords = "CRISPR/Cas9, delivery, genome editing, ribonucleoprotein complexes",
author = "Amirkhanov, {R. N.} and Stepanov, {G. A.}",
year = "2019",
month = nov,
day = "1",
doi = "10.1134/S1068162019060025",
language = "English",
volume = "45",
pages = "431--437",
journal = "Russian Journal of Bioorganic Chemistry",
issn = "1068-1620",
publisher = "MAIK NAUKA/INTERPERIODICA/SPRINGER",
number = "6",

}

RIS

TY - JOUR

T1 - Systems of Delivery of CRISPR/Cas9 Ribonucleoprotein Complexes for Genome Editing

AU - Amirkhanov, R. N.

AU - Stepanov, G. A.

PY - 2019/11/1

Y1 - 2019/11/1

N2 - The discovery of RNA-guided nucleases have enabled to leap forward in genome editing of cells and organisms. These nucleases can be delivered into cells as plasmid DNA, mRNA or ribonucleoprotein complexes (RNPs). The delivery in the form of RNP has some advantages because the target gene editing begins immediately without the process of intracellular synthesis of components and CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9 (CRISPR associated protein 9) system assembly. This strategy makes it possible to directly control RNP concentration and to decrease the number of off-targets due to rapid degradation of the complex in the cell. However, the task to develop RNP delivery systems remains unsolved. This review is devoted to RNP delivery into cells and tissues using physical approaches and different carriers. Special attention is paid to novel approaches that improve the RNP delivery efficiency.

AB - The discovery of RNA-guided nucleases have enabled to leap forward in genome editing of cells and organisms. These nucleases can be delivered into cells as plasmid DNA, mRNA or ribonucleoprotein complexes (RNPs). The delivery in the form of RNP has some advantages because the target gene editing begins immediately without the process of intracellular synthesis of components and CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9 (CRISPR associated protein 9) system assembly. This strategy makes it possible to directly control RNP concentration and to decrease the number of off-targets due to rapid degradation of the complex in the cell. However, the task to develop RNP delivery systems remains unsolved. This review is devoted to RNP delivery into cells and tissues using physical approaches and different carriers. Special attention is paid to novel approaches that improve the RNP delivery efficiency.

KW - CRISPR/Cas9

KW - delivery

KW - genome editing

KW - ribonucleoprotein complexes

UR - http://www.scopus.com/inward/record.url?scp=85078604527&partnerID=8YFLogxK

U2 - 10.1134/S1068162019060025

DO - 10.1134/S1068162019060025

M3 - Review article

AN - SCOPUS:85078604527

VL - 45

SP - 431

EP - 437

JO - Russian Journal of Bioorganic Chemistry

JF - Russian Journal of Bioorganic Chemistry

SN - 1068-1620

IS - 6

ER -

ID: 23570221