Developing an Anion Exchange Chromatography Assay for Determining Empty and Full Capsid Contents in AAV6.2

被引:76
作者
Wang, Chunlei [1 ]
Mulagapati, Sri Hari Raju [1 ]
Chen, Zhongying [1 ]
Du, Jing [1 ]
Zhao, Xiaohui [1 ]
Xi, Guoling [2 ]
Chen, Liyan [2 ]
Linke, Thomas [2 ]
Gao, Cuihua [3 ]
Schmelzer, Albert E. [4 ]
Liu, Dengfeng [1 ]
机构
[1] AstraZeneca, BioPharmaceut R&D, Analyt Sci, Biopharmaceut Dev, One MedImmune Way, Gaithersburg, MD 20878 USA
[2] AstraZeneca, BioPharmaceut R&D, Purificat Proc Sci, Biopharmaceut Dev, One MedImmune Way, Gaithersburg, MD 20878 USA
[3] AstraZeneca, R&D, Antibody Discovery & Prot Engn, One MedImmune Way, Gaithersburg, MD 20878 USA
[4] AstraZeneca, BioPharmaceut R&D, Biopharmaceut Dev, Cell Culture & Fermentat Sci, One MedImmune Way, Gaithersburg, MD 20878 USA
关键词
GENE-THERAPY; VECTORS; PURIFICATION; ULTRACENTRIFUGATION; POLIOVIRUS; PARTICLES; GENOME;
D O I
10.1016/j.omtm.2019.09.006
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Adeno-associated virus (AAV) vectors are clinically proven gene delivery vehicles that are attracting an increasing amount of attention. Non-genome-containing empty AAV capsids are by-products during AAV production that have been reported to potentially impact AAV product safety and efficacy. Therefore, the presence and amount of empty AAV capsids need to be characterized during process development. Multiple methods have been reported to characterize empty AAV capsid levels, including transmission electron microscopy (TEM), analytical ultracentrifugation (AUC), charge detection mass spectrometry (CDMS), UV spectrophotometry, and measuring capsid and genome copies by ELISA and qPCR. However, these methods may lack adequate accuracy and precision or be challenging to transfer to a quality control (QC) lab due to the difficulty of implementation. In this study, we used AAV serotype 6.2 (AAV6.2) as an example to show the development of a QC-friendly anion exchange chromatography (AEX) assay for the determination of empty and full capsid percentages. The reported assay requires several microliters of material with a minimum titer of 5 x 10(11) vg/mL, and it can detect the presence of as low as 2.9% empty capsids in AAV6.2 samples. Additionally, the method is easy to deploy, can be automated, and has been successfully implemented to support testing of various in-process and release samples.
引用
收藏
页码:257 / 263
页数:7
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