遗传增强
病毒载体
干细胞
色谱法
化学
离心
细胞
分子生物学
基因
生物
细胞生物学
生物化学
重组DNA
作者
Hazal Banu Olgun,Hale M. Tasyurek,Ahter Dilşad Şanlioğlu,Salih Şanlıoğlu
出处
期刊:Methods in molecular biology
日期:2018-01-01
卷期号:: 347-365
被引量:19
标识
DOI:10.1007/7651_2018_154
摘要
Lentiviral vectors (LVs) have been increasingly used in clinical gene therapy applications particularly due to their efficient gene transfer ability, lack of interference from preexisting viral immunity, and long-term gene expression they provide. Purity of LVs is essential in in vivo applications, for a high therapeutic benefit with minimum toxicity. Accordingly, laboratory scale production of LVs frequently involves transient cotransfection of 293T cells with packaging and transfer plasmids in the presence of CaPO4. After clearance of the cellular debris by low-speed centrifugation and filtration, lentivectors are usually concentrated by high-speed ultracentrifugation in sucrose cushion. Concentrated viral samples are then purified by anion exchange chromatography (AEX) after benzonase treatment to remove the residual cellular DNA. Here, we describe an improved practical method for LV purification using AEX, useful for experimental studies concerning gene and stem cell therapy.
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