Efficient gene editing via non-viral delivery of CRISPR-Cas9 system using polymeric and hybrid microcarriers; Nanomedicine: Nanotechnology, Biology and Medicine; Vol. 14, iss. 1

Մատենագիտական մանրամասներ
Parent link:Nanomedicine: Nanotechnology, Biology and Medicine
Vol. 14, iss. 1.— 2018.— [P. 97-108]
Համատեղ հեղինակ: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Այլ հեղինակներ: Timin A. S. Aleksandr Sergeevich, Muslimov A. R. Albert Radikovich, Epifanovskaya O. S., Shakirova A. I., Mock U. Ulrike, Riecken K. Kristoffer, Okilova M. V., Sergeev V. S., Afanasyev B. V., Fehse B., Sukhorukov G. B.
Ամփոփում:Title screen
CRISPR-Cas9 is a revolutionary genome-editing technology that has enormous potential for the treatment of genetic diseases. However, the lack of efficient and safe, non-viral delivery systems has hindered its clinical application. Here, we report on the application of polymeric and hybrid microcarriers, made of degradable polymers such as polypeptides and polysaccharides and modified by silica shell, for delivery of all CRISPR-Cas9 components. We found that these microcarriers mediate more efficient transfection than a commercially available liposome-based transfection reagent (>70% vs. <50% for mRNA, >40% vs. 20% for plasmid DNA). For proof-of-concept, we delivered CRISPR-Cas9 components using our capsules to dTomato-expressing HEK293T cells-a model, in which loss of red fluorescence indicates successful gene editing. Notably, transfection of indicator cells translated in high-level dTomato knockout in approx. 70% of transfected cells. In conclusion, we have provided proof-of-principle that our micro-sized containers represent promising non-viral platforms for efficient and safe gene editing.
Режим доступа: по договору с организацией-держателем ресурса
Լեզու:անգլերեն
Հրապարակվել է: 2018
Խորագրեր:
Առցանց հասանելիություն:https://doi.org/10.1016/j.nano.2017.09.001
Ձևաչափ: Էլեկտրոնային Գրքի գլուխ
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667304

MARC

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200 1 |a Efficient gene editing via non-viral delivery of CRISPR-Cas9 system using polymeric and hybrid microcarriers  |f A. S. Timin, A. R. Muslimov, O. S. Epifanovskaya [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 46 tit.] 
330 |a CRISPR-Cas9 is a revolutionary genome-editing technology that has enormous potential for the treatment of genetic diseases. However, the lack of efficient and safe, non-viral delivery systems has hindered its clinical application. Here, we report on the application of polymeric and hybrid microcarriers, made of degradable polymers such as polypeptides and polysaccharides and modified by silica shell, for delivery of all CRISPR-Cas9 components. We found that these microcarriers mediate more efficient transfection than a commercially available liposome-based transfection reagent (>70% vs. <50% for mRNA, >40% vs. 20% for plasmid DNA). For proof-of-concept, we delivered CRISPR-Cas9 components using our capsules to dTomato-expressing HEK293T cells-a model, in which loss of red fluorescence indicates successful gene editing. Notably, transfection of indicator cells translated in high-level dTomato knockout in approx. 70% of transfected cells. In conclusion, we have provided proof-of-principle that our micro-sized containers represent promising non-viral platforms for efficient and safe gene editing. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Nanomedicine: Nanotechnology, Biology and Medicine 
463 |t Vol. 14, iss. 1  |v [P. 97-108]  |d 2018 
610 1 |a электронный ресурс 
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610 1 |a gene delivery 
610 1 |a CRISPR–Cas9 
610 1 |a gene editing 
610 1 |a polyelectrolyte microcapsules 
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610 1 |a гены 
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701 1 |a Muslimov  |b A. R.  |g Albert Radikovich 
701 1 |a Epifanovskaya  |b O. S. 
701 1 |a Shakirova  |b A. I. 
701 1 |a Mock  |b U.  |g Ulrike 
701 1 |a Riecken  |b K.  |g Kristoffer 
701 1 |a Okilova  |b M. V. 
701 1 |a Sergeev  |b V. S. 
701 1 |a Afanasyev  |b B. V. 
701 1 |a Fehse  |b B. 
701 1 |a Sukhorukov  |b G. B. 
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