Quantitation of adenovirus DNA and virus particles with the PicoGreen fluorescent dye

被引:76
作者
Murakami, P [1 ]
McCaman, MT [1 ]
机构
[1] Berlex Biosci, Proc Dev Dept, Richmond, CA 94804 USA
关键词
adenovirus; DNA quantitation; fluorescence particle number; PicoGreen;
D O I
10.1006/abio.1999.4282
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A microplate assay for the rapid quantitation of adenovirus DNA has been developed using the fluorescent dye PicoGreen, which selectively binds double-stranded DNA. The method was first applied to extracted adenoviral DNA and then extended to samples of intact, purified adenovirus after lysis of the viral capsid with the ionic detergent SDS. Utilizing the stoichiometric relationship between adenovirus DNA and intact particles, a physical particle count of intact virus is then derived for the sample. This PicoGreen-based assay has excellent reproducibility, linearity, and sensitivity. In its present form, this assay has a limit of quantitation of 10.3 ng/ml viral DNA, predicted to correspond to 2.6 x 10(8) virus particles/ml. This procedure was compared to a widely utilized spectroscopic method, in which samples are lysed with SDS and absorbance is read at 260 nm, and found to be 10- to 20-fold more sensitive. The dye binding assay also uses considerably less sample volume (<20%) than that needed for the spectroscopic method. Particle count values generated by the PicoGreen procedure are consistently lower (typically 1.5- to 2-fold) than this spectroscopic method. The applications and limitations of this method in the analysis of adenovirus samples are discussed. (C) 1999 Academic Press.
引用
收藏
页码:283 / 288
页数:6
相关论文
共 14 条
  • [1] PicoGreen quantitation of DNA: Effective evaluation of samples pre- or post-PCR
    Ahn, SJ
    Costa, J
    Emanuel, JR
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (13) : 2623 - 2625
  • [2] ADENOVIRUS-MEDIATED IN-VIVO GENE-TRANSFER
    BRODY, SL
    CRYSTAL, RG
    [J]. GENE THERAPY FOR NEOPLASTIC DISEASES, 1994, 716 : 90 - 103
  • [3] IMPROVED MICRO-FLUOROMETRIC DNA DETERMINATION IN BIOLOGICAL-MATERIAL USING 33258-HOECHST
    CESARONE, CF
    BOLOGNESI, C
    SANTI, L
    [J]. ANALYTICAL BIOCHEMISTRY, 1979, 100 (01) : 188 - 197
  • [4] Analytical methods for the characterization of cationic lipid nucleic acid complexes
    Ferrari, ME
    Nguyen, CM
    Zelphati, O
    Tsai, YL
    Felgner, PL
    [J]. HUMAN GENE THERAPY, 1998, 9 (03) : 341 - 351
  • [6] PURIFICATION OF A TYPE-5 RECOMBINANT ADENOVIRUS ENCODING HUMAN P53 BY COLUMN CHROMATOGRAPHY
    HUYGHE, BG
    LIU, XD
    SUTJIPTO, S
    SUGARMAN, BJ
    HORN, MT
    SHEPARD, HM
    SCANDELLA, CJ
    SHABRAM, P
    [J]. HUMAN GENE THERAPY, 1995, 6 (11) : 1403 - 1416
  • [7] LEHMBERG E, 1999, IN PRESS J CHROMATOG
  • [8] Regional angiogenesis induced in nonischemic tissue by an adenoviral vector expressing vascular endothelial growth factor
    Magovern, CJ
    Mack, CA
    Zhang, J
    Rosengart, TK
    Isom, OW
    Crystal, RG
    [J]. HUMAN GENE THERAPY, 1997, 8 (02) : 215 - 227
  • [9] POLYPEPTIDES OF ADENOVIRUS .I. EVIDENCE FOR MULTIPLE PROTEIN COMPONENTS IN VIRION AND A COMPARISON OF TYPES 2 7A AND 12
    MAIZEL, JV
    WHITE, DO
    SCHARFF, MD
    [J]. VIROLOGY, 1968, 36 (01) : 115 - +
  • [10] Evaluation of the concentration and bioactivity of adenovirus vectors for gene therapy
    Mittereder, N
    March, KL
    Trapnell, BC
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (11) : 7498 - 7509