质粒
载体(分子生物学)
基因表达
生物
分子生物学
遗传增强
细胞生物学
基因
差速器(机械装置)
表达式向量
重组DNA
转染
基因传递
细胞培养
基因表达调控
病毒学
HEK 293细胞
病毒载体
作者
Laura Van Lieshout,Katrina Costa-Grant,Dimpal Lata,Alejo Zacarias,Stacy Ota,Annie Adusei,Devin Schroeder,Diane Golebiowski,Ifeyinwa Iwuchukwu
标识
DOI:10.1038/s41434-026-00637-x
摘要
Helper plasmids that depend on native adenovirus gene expression have long been the standard for transient adeno-associated virus (AAV) production. Here, we demonstrate that engineering the required helper gene expression can greatly increase AAV production relative to the use of native adenovirus gene regulation. Two different engineered helper plasmid designs improved AAV vector genome (VG) titers up to 5-fold compared to a standard helper plasmid. A substantial decrease in adenovirus E4orf6 and an increase in L4 22K and 33K gene expression were associated with the improved engineered helper plasmids. VG titer improvement across capsid serotypes, plasmid transfection platforms and genome designs suggest that engineering helper gene expression is widely suited to improving AAV manufacturing yields while also maintaining consistent vector quality attributes.
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