Separation of adeno-associated virus type 2 empty particles from genome containing vectors by anion-exchange column chromatography

被引:121
|
作者
Qu, Guang
Bahr-Davidson, Jennifer
Prado, Joseph
Tai, Alex
Cataniag, Floro
McDonnell, Jennifer
Zhou, Jingmin
Hauck, Bernd
Luna, Jac
Sommer, Jurg M.
Smith, Peter
Zhou, Shangzhen
Colosi, Peter
High, Katherine A.
Pierce, Glenn F.
Wright, J. Fraser
机构
[1] Childrens Hosp Philadelphia, Ctr Cellular & Mol Therapeut, Philadelphia, PA 19104 USA
[2] Avigen Inc, Alameda, CA 94502 USA
[3] Childrens Hosp Philadelphia, Howard Hughes Med Inst, Philadelphia, PA 19104 USA
关键词
adeno-associoted virus; empty capsids; column chromatography;
D O I
10.1016/j.jviromet.2006.11.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Adeno-associated virus (AAV) empty capsids typically co-purify with genome containing AAV2 vectors purified by Column chromatography. This study describes a method to remove empty capsids front genome containing vector particles by anion exchange chromatography. The separation is based on the slightly less anionic character of empty particles compared to vectors. Detailed methods to achieve AAV2 vector purification and particle separation using cation exchange resin POROS 50HS followed by anion exchange resin Q-Sepharose(x1) are described. Chromatographic separation of AAV2 particles was achieved using gradients based on sodium acetate and ammonium acetate, and was optinnal at pH 8.5. Efficient romoval of particle surface nucleic acid impurities was found to be important to achieve good particle, separation. In a large scale experiment performed using partially purified vector containing a Mixture of 1.56 x 10(14) vg and 2.52 x 10(15) empty capsids as a starting material, the optimized containing 0.25 x 10(14) empty capsids, corresponding to 74% anion exchange chrometography method resulted in a vector peak of 1.15 x 10(14) vg vector yield and 86-fold reduction in empty capsids in the vector product. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 192
页数:10
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