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Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield
被引:1053
作者:
Zolotukhin, S
Byrne, BJ
Mason, E
Zolotukhin, I
Potter, M
Chesnut, K
Summerford, C
Samulski, RJ
Muzyczka, N
机构:
[1] Univ Florida, Coll Med, Gene Therapy Ctr, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Med, Dept Pediat, Gainesville, FL 32610 USA
[4] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC USA
[5] Univ N Carolina, Gene Therapy Ctr, Chapel Hill, NC USA
来源:
关键词:
adeno-associated virus;
rAAV;
gene therapy;
vector production;
vector purification;
D O I:
10.1038/sj.gt.3300938
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Conventional methods for rAAV purification that are based on cesium chloride ultracentrifugation have often produced vector preparations of variable quality and resulted in significant loss of particle infectivity. We report here several novel purification strategies that involve the use of non-ionic iodixanol gradients followed by ion exchange or heparin affinity chromatography by either conventional or HPLC columns. These methods result in more than 50% recovery of rAAV from a crude lysate and routinely produce vector that is more than 99% pure. More importantly, the new purification procedures consistently produce rAAV stocks with particle-to-infectivity ratios of less than 100, which is significantly better than conventional methods. The new protocol increases the overall yield of infectious rAAV by at least 10-fold and allows for the complete purification of rAAV in 1 working day. Several of these methods should also be useful for large-scale production.
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页码:973 / 985
页数:13
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