生物制造
效价
病毒
转染
腺相关病毒
体内
质粒
生物反应器
分子生物学
重组DNA
共焦
污渍
化学
生物
病毒学
细胞培养
基因
生物技术
载体(分子生物学)
生物化学
遗传学
几何学
有机化学
数学
作者
Kai Chen,Seulhee Kim,Siying Yang,Tanvi Varadkar,Zhuoxin Zhou,Jiashuai Zhang,Lufang Zhou,Margaret Liu
标识
DOI:10.1186/s13036-024-00409-4
摘要
Abstract Recombinant adeno-associated virus (rAAV) has been developed as a safe and effective gene delivery vehicle to treat rare genetic diseases. This study aimed to establish a novel biomanufacturing process to achieve high production and purification of various AAV serotypes (AAV2, 5, DJ, DJ8). First, a robust suspensive production process was developed and optimized using Gibco Viral Production Cell 2.0 in 30–60 mL shaker flask cultures by evaluating host cells, cell density at the time of transfection and plasmid amount, adapted to 60–100 mL spinner flask production, and scaled up to 1.2–2.0-L stirred-tank bioreactor production at 37 °C, pH 7.0, 210 rpm and DO 40%. The optimal process generated AAV titer of 7.52–8.14 × 10 10 vg/mL. Second, a new AAV purification using liquid chromatography was developed and optimized to reach recovery rate of 85–95% of all four serotypes. Post-purification desalting and concentration procedures were also investigated. Then the generated AAVs were evaluated in vitro using Western blotting, transmission electron microscope, confocal microscope and bioluminescence detection. Finally, the in vivo infection and functional gene expression of AAV were confirmed in tumor xenografted mouse model. In conclusion, this study reported a robust, scalable, and universal biomanufacturing platform of AAV production, clarification and purification.
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