Scalable purification of adeno-associated virus type 2, 4, or 5 using ion-exchange chromatography

被引:126
作者
Kaludov, N [1 ]
Handelman, B [1 ]
Chiorini, JA [1 ]
机构
[1] Natl Inst Dent & Cranialfacial Res, Gene Therapy & Therapeut Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1089/104303402320139014
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The availability of high-titer, high-purity, adeno-associated virus type 2 (AAV2) stocks has dramatically increased our understanding of this virus and its utility as a gene transfer vector. Current methods of purification take advantage of the stable interaction of AAV2 with heparin sulfate. This affinity chromatography, however, is not useful for purifying AAV4 and AAV5, because these serotypes lack heparin-binding activity. We have developed simple ion exchange high-performance liquid chromatography (HPLC) method for purifying different AAV serotypes that does not rely on the affinity of the viruses for heparin. The protocol is fast, efficient, and yields highly infectious material. Analysis of the highly purified virus indicated that more than 90% of the particles contained genomes and were more active than virus purified by cesium chloride (CsCl) gradient purification. This procedure is scalable and can easily be streamlined for large-scale production of recombinant adeno-associated virus (rAAV), regardless of the serotype. Ultimately, the new purification method will further the characterization of rAAV of different serotypes as vectors for gene therapy applications.
引用
收藏
页码:1235 / 1243
页数:9
相关论文
共 17 条
  • [1] DNA-DAMAGING AGENTS GREATLY INCREASE THE TRANSDUCTION OF NONDIVIDING CELLS BY ADENOASSOCIATED VIRUS VECTORS
    ALEXANDER, IE
    RUSSELL, DW
    MILLER, AD
    [J]. JOURNAL OF VIROLOGY, 1994, 68 (12) : 8282 - 8287
  • [2] Transduction of murine cerebellar neurons with recombinant FIV and AAV5 vectors
    Alisky, JM
    Hughes, SM
    Sauter, SL
    Jolly, D
    Dubensky, TW
    Staber, PD
    Chiorini, JA
    Davidson, BL
    [J]. NEUROREPORT, 2000, 11 (12) : 2669 - 2673
  • [3] A single-step affinity column for purification of serotype-5 based adeno-associated viral vectors
    Auricchio, A
    O'Connor, E
    Hildinger, M
    Wilson, JM
    [J]. MOLECULAR THERAPY, 2001, 4 (04) : 372 - 374
  • [4] Cloning of adeno-associated virus type 4 (AAV4) and generation of recombinant AAV4 particles
    Chiorini, JA
    Yang, L
    Liu, YJ
    Safer, B
    Kotin, RM
    [J]. JOURNAL OF VIROLOGY, 1997, 71 (09) : 6823 - 6833
  • [5] Cloning and characterization of adeno-associated virus type 5
    Chiorini, JA
    Kim, F
    Yang, L
    Kotin, RM
    [J]. JOURNAL OF VIROLOGY, 1999, 73 (02) : 1309 - 1319
  • [6] Highly purified recombinant adeno-associated virus vectors are biologically active and free of detectable helper and wild-type viruses
    Clark, KR
    Liu, XL
    McGrath, JP
    Johnson, PR
    [J]. HUMAN GENE THERAPY, 1999, 10 (06) : 1031 - 1039
  • [7] Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus
    Flannery, JG
    Zolotukhin, S
    Vaquero, MI
    LaVail, MM
    Muzyczka, N
    Hauswirth, WW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) : 6916 - 6921
  • [8] Adeno-associated virus serotype 4 (AAV4) and AAV5 both require sialic acid binding for hemagglutination and efficient transduction but differ in sialic acid linkage specificity
    Kaludov, N
    Brown, KE
    Walters, RW
    Zabner, J
    Chiorini, JA
    [J]. JOURNAL OF VIROLOGY, 2001, 75 (15) : 6884 - 6893
  • [9] LONG-TERM GENE-EXPRESSION AND PHENOTYPIC CORRECTION USING ADENOASSOCIATED VIRUS VECTORS IN THE MAMMALIAN BRAIN
    KAPLITT, MG
    LEONE, P
    SAMULSKI, RJ
    XIAO, X
    PFAFF, DW
    OMALLEY, KL
    DURING, MJ
    [J]. NATURE GENETICS, 1994, 8 (02) : 148 - 154
  • [10] Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector
    McCown, TJ
    Xiao, X
    Li, J
    Breese, GR
    Samulski, RJ
    [J]. BRAIN RESEARCH, 1996, 713 (1-2) : 99 - 107