Zeta potential of transfection complexes formed in serum-free medium call predict in vitro gene transfer efficiency of transfection reagent

被引:41
作者
Son, KK [1 ]
Tkach, D [1 ]
Patel, DH [1 ]
机构
[1] Rutgers State Univ, Coll Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2000年 / 1468卷 / 1-2期
关键词
zeta potential; liposome-mediated gene transfer; polycation; particle size;
D O I
10.1016/S0005-2736(00)00312-6
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
We have tested the zeta potential (zeta, the surface charge density) of transfection complexes formed in serum-free medium as a rapid and reliable technique for screening transfection efficiency of a new reagent or formulation. The complexes of CAT plasmid DNA (1 mu g) and DC-chol/DOPE liposomes (3-20 nmol) were largely negatively charged (zeta= -15 to -21 mV), which became neutral or positive as 0.5 mu g or a higher amount of poly-L-lysine (PLL, MW 29 300 or MW 204 000) was added (-3.16 +/- 3,47 to +6.04 +/- 2.23 mV). However, the complexes of CAT plasmid DNA (1 mu g) and PLL MW 29 300 (0.5 mu g or higher) were neutral or positively charged (-3.22 +/- 2.3 to +5.55 +/- 0.64 mV), which remained the same as 6.6 nmol of the liposomes was added. The complexes formed between two positively charged compounds, PLL MW 29 300 (0.5 mu g) and the liposomes (3.20 nmol), were as closely positively charged as DNA/PLL or DNA/liposomes/PLL complexes (+3.31 +/- 0.41 to 7.16 +/- 1.0 mV). These results indicate that PLL determined the overall charge of the DNA/liposome/PLL ternary complexes. The complexes formed with histone (0.75 mu g or higher) were also positively charged, whose transfection activity was as high as PLL MW 39 300. However, the complexes formed with protamine or PLL MW 2400 remained negatively charged. These observations are in good agreement with the transfection activity of the formulation containing each polycationic polymer. The presence of PLL MW 29 300 did not change the hydrodynamic diameter of DNA/liposome/PLL complexes (d(H) = 275-312 nm). The complexes made of different sizes of PLL (MW 3400 and 204 000) also did not significantly change their size. This suggests that DNA condensation may not be critical. Therefore, zeta of the transfection complex can predict the transfection efficiency of a new formulation or reagent. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 14
页数:4
相关论文
共 11 条
  • [1] A physicochemical approach for predicting the effectiveness of peptide-based gene delivery systems for use in plasmid-based gene therapy
    Duguid, JG
    Li, C
    Shi, M
    Logan, MJ
    Alila, H
    Rolland, A
    Tomlinson, E
    Sparrow, JT
    Smith, LC
    [J]. BIOPHYSICAL JOURNAL, 1998, 74 (06) : 2802 - 2814
  • [2] Potentiation of cationic liposome-mediated gene delivery by polycations
    Gao, X
    Huang, L
    [J]. BIOCHEMISTRY, 1996, 35 (03) : 1027 - 1036
  • [3] A NOVEL CATIONIC LIPOSOME REAGENT FOR EFFICIENT TRANSFECTION OF MAMMALIAN-CELLS
    GAO, X
    HUANG, L
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (01) : 280 - 285
  • [4] MODE OF FORMATION AND STRUCTURAL FEATURES OF DNA CATIONIC LIPOSOME COMPLEXES USED FOR TRANSFECTION
    GERSHON, H
    GHIRLANDO, R
    GUTTMAN, SB
    MINSKY, A
    [J]. BIOCHEMISTRY, 1993, 32 (28) : 7143 - 7151
  • [5] RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS
    GORMAN, CM
    MOFFAT, LF
    HOWARD, BH
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) : 1044 - 1051
  • [6] Liposomal gene delivery: A complex package
    Huang, L
    Li, S
    [J]. NATURE BIOTECHNOLOGY, 1997, 15 (07) : 620 - 621
  • [7] An inverted hexagonal phase of cationic liposome-DNA complexes related to DNA release and delivery
    Koltover, I
    Salditt, T
    Rädler, JO
    Safinya, CR
    [J]. SCIENCE, 1998, 281 (5373) : 78 - 81
  • [8] DIRECT GENE-TRANSFER WITH DNA LIPOSOME COMPLEXES IN MELANOMA - EXPRESSION, BIOLOGIC ACTIVITY, AND LACK OF TOXICITY IN HUMANS
    NABEL, GJ
    NABEL, EG
    YANG, ZY
    FOX, BA
    PLAUTZ, GE
    GAO, X
    HUANG, L
    SHU, SY
    GORDON, D
    CHANG, AE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) : 11307 - 11311
  • [9] SON KK, 2000, BIOCHIM BIOPHYS ACTA, V1466, P1
  • [10] GENE-TRANSFER INVIVO WITH DNA LIPOSOME COMPLEXES - SAFETY AND ACUTE TOXICITY IN MICE
    STEWART, MJ
    PLAUTZ, GE
    DELBUONO, L
    YANG, ZY
    XU, L
    GAO, X
    HUANG, L
    NABEL, EG
    NABEL, GJ
    [J]. HUMAN GENE THERAPY, 1992, 3 (03) : 267 - 275