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
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.
引用
收藏
页码:973 / 985
页数:13
相关论文
共 38 条
[11]   STABLE IN-VIVO EXPRESSION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR WITH AN ADENOASSOCIATED VIRUS VECTOR [J].
FLOTTE, TR ;
AFIONE, SA ;
CONRAD, C ;
MCGRATH, SA ;
SOLOW, R ;
OKA, H ;
ZEITLIN, PL ;
GUGGINO, WB ;
CARTER, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) :10613-10617
[12]   Novel tools for production and purification of recombinant adenoassociated virus vectors [J].
Grimm, D ;
Kern, A ;
Rittner, K ;
Kleinschmidt, JA .
HUMAN GENE THERAPY, 1998, 9 (18) :2745-2760
[13]   Construction of adenovirus vectors through Cre-lox recombination [J].
Hardy, S ;
Kitamura, M ;
HarrisStansil, T ;
Dai, YM ;
Phipps, ML .
JOURNAL OF VIROLOGY, 1997, 71 (03) :1842-1849
[14]  
HEIM R, 1996, J VIROL, V70, P4646
[15]   USE OF ADENO-ASSOCIATED VIRUS AS A MAMMALIAN DNA CLONING VECTOR - TRANSDUCTION OF NEOMYCIN RESISTANCE INTO MAMMALIAN TISSUE-CULTURE CELLS [J].
HERMONAT, PL ;
MUZYCZKA, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (20) :6466-6470
[16]   GENETICS OF ADENO-ASSOCIATED VIRUS - ISOLATION AND PRELIMINARY CHARACTERIZATION OF ADENO-ASSOCIATED VIRUS TYPE-2 MUTANTS [J].
HERMONAT, PL ;
LABOW, MA ;
WRIGHT, R ;
BERNS, KI ;
MUZYCZKA, N .
JOURNAL OF VIROLOGY, 1984, 51 (02) :329-339
[17]   IDENTIFICATION OF STRUCTURAL FEATURES OF HEPARIN REQUIRED FOR INHIBITION OF HERPES-SIMPLEX VIRUS TYPE-1 BINDING [J].
HEROLD, BC ;
GERBER, SI ;
POLONSKY, T ;
BELVAL, BJ ;
SHAKLEE, PN ;
HOLME, K .
VIROLOGY, 1995, 206 (02) :1108-1116
[18]   Packaging cells based on inducible gene amplification for the production of adeno-associated virus vectors [J].
Inoue, N ;
Russell, DW .
JOURNAL OF VIROLOGY, 1998, 72 (09) :7024-7031
[19]   Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers [J].
Jooss, K ;
Yang, YP ;
Fisher, KJ ;
Wilson, JM .
JOURNAL OF VIROLOGY, 1998, 72 (05) :4212-4223
[20]   Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic protein [J].
Kessler, PD ;
Podsakoff, GM ;
Chen, XJ ;
McQuiston, SA ;
Colosi, PC ;
Matelis, LA ;
Kurtzman, GJ ;
Byrne, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :14082-14087