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1.
Mol Biotechnol ; 64(12): 1376-1387, 2022 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-35670994

RESUMEN

The discovery of bacterial-derived Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system has revolutionized genome engineering and gene therapy due to its wide range of applications. One of the major challenging issues in CRISPR/Cas system is the lack of an efficient, safe, and clinically suitable delivery of the system's components into target cells. Here, we describe the development of polyethylenimine coated-bovine serum albumin nanoparticles (BSA-PEI NPs) for efficient delivery of CRISPR/Cas9 system in both DNA (px458 plasmid) and ribonucleoprotein (RNP) forms into MDA-MB-231 human breast cancer cell line. Our data showed that synthesized BSA-PEI (BP) NPs delivered plasmid px458 at concentrations of 0.15, 0.25, and 0.35 µg/µl with efficiencies of approximately 29.7, 54.8, and 84.1% into MDA-MB-231 cells, respectively. Our study demonstrated that Cas9/sgRNA RNP complex efficiently (~ 92.6%) delivered by BSA-PEI NPs into the same cells. Analysis of toxicity and biocompatibility of synthesized NPs on human red blood cells, MDA-MB-231 cells, and mice showed that the selected concentration (28 µg/µl) of BSA-PEI NPs for transfection had no remarkable toxicity effects. Thus, obtained results suggest BSA-PEI NPs as one of the most promising carrier for delivering CRISPR/Cas9 to target cells.


Asunto(s)
Sistemas CRISPR-Cas , Nanopartículas , Animales , Proteína 9 Asociada a CRISPR/genética , Humanos , Ratones , Polietileneimina , Ribonucleoproteínas/genética , Ribonucleoproteínas/metabolismo , Albúmina Sérica Bovina
2.
Folia Histochem Cytobiol ; 58(3): 163-173, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32978771

RESUMEN

Clustered Regulatory Interspaced Short Palindromic Repeats (CRISPR) is one of the major genome editing systems and allows changing DNA levels of an organism. Among several CRISPR categories, the CRISPR-Cas9 system has shown a remarkable progression rate over its lifetime. Recently, other tools including CRISPR-Cas12 and CRISPR-Cas13 have been introduced. CRISPR-Cas9 system has played a key role in the industrial cell factory's production and improved our understanding of genome function. Additionally, this system has been used as one of the major genome editing systems for the diagnosis and treatment of several infectious and non-infectious diseases. In this review, we discuss CRISPR biology, its versatility, and its application in biomedical engineering.


Asunto(s)
Ingeniería Biomédica/métodos , Sistemas CRISPR-Cas , Animales , Ingeniería Celular , Descubrimiento de Drogas , Edición Génica/métodos , Humanos , Modelos Biológicos
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