Comparison of different commercially available cationic lipid-based transfection kits

被引:34
作者
Simberg, D [1 ]
Hirsch-Lerner, D [1 ]
Nissim, R [1 ]
Barenholz, Y [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Lab Membrane & Liposome, Res Dept Biochem, IL-91120 Jerusalem, Israel
关键词
cationic lipids; gene delivery; commercial transfection kits; stability;
D O I
10.3109/08982100009031091
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
Cationic lipid-containing nonviral vectors for intracellular DNA delivery (lipoplexes) are becoming an important tool in a number of applications in life sciences, biotechnology, agriculture, and medicine. They became a biotechnology industry product on their own, being marketed as transfection kits. Their number on the market, now exceeding 50, is growing steadily. Life science researchers could face a problem having such a large choice of products. In such a situation, a straightforward comparison of existing transfection kits is useful. Therefore, several new proprietary transfection kits (Effectene, FuGENE 6, GeneSHUTTLE-20, GeneSHUTTLE-40, and GenePORTER Transfection Reagents), as well as well-established ones of known composition (Lipofectin, LipofectAmine, DOSPER, and DOTAP Transfection Reagents) were chosen for simultaneous comparison of their in vitro activity and shelf stability. Using expression of human growth hormone in NIH 3T3 cells, it was shown that most of the kits show roughly the same order of magnitude of transfection, with FuGENE 6 and GeneSHUTTLE-40 being somewhat better. In parallel, stability tests were performed to assess the degree of lipid hydrolysis in different kits. It was shown that in all kits, level of non-esterified fatty acids increased upon storage at 4 degrees C in aqueous dispersion, suggesting base-catalyzed hydrolysis of the ester lipids. The pattern of degradation was also clearly visible when lipid kit components were analyzed on TLC plates.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 18 条
[1]   Green fluorescent protein as a real time quantitative reporter of heterologous protein production [J].
Albano, CR ;
Randers-Eichhorn, L ;
Bentley, WE ;
Rao, G .
BIOTECHNOLOGY PROGRESS, 1998, 14 (02) :351-354
[2]   Biophysical characterization of cationic lipid:DNA complexes [J].
Eastman, SJ ;
Siegel, C ;
Tousignant, J ;
Smith, AE ;
Cheng, SH ;
Scheule, RK .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1997, 1325 (01) :41-62
[3]   Analytical methods for the characterization of cationic lipid nucleic acid complexes [J].
Ferrari, ME ;
Nguyen, CM ;
Zelphati, O ;
Tsai, YL ;
Felgner, PL .
HUMAN GENE THERAPY, 1998, 9 (03) :341-351
[4]   MODE OF FORMATION AND STRUCTURAL FEATURES OF DNA CATIONIC LIPOSOME COMPLEXES USED FOR TRANSFECTION [J].
GERSHON, H ;
GHIRLANDO, R ;
GUTTMAN, SB ;
MINSKY, A .
BIOCHEMISTRY, 1993, 32 (28) :7143-7151
[5]  
Kao MC, 1998, ONCOL REP, V5, P625
[6]   Atomic force microscopy for studying gene transfection mediated by cationic liposomes with a cationic cholesterol derivative [J].
Kawaura, C ;
Noguchi, A ;
Furuno, T ;
Nakanishi, M .
FEBS LETTERS, 1998, 421 (01) :69-72
[7]  
LASIC DD, 1997, LIPOSOMES GENE DELIV
[8]   OLIGOPYRIMIDINE TRACT AT THE 5' END OF MAMMALIAN RIBOSOMAL-PROTEIN MESSENGER-RNAS IS REQUIRED FOR THEIR TRANSLATIONAL CONTROL [J].
LEVY, S ;
AVNI, D ;
HARIHARAN, N ;
PERRY, RP ;
MEYUHAS, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (08) :3319-3323
[9]   Cationic lipid-mediated transfection of cells in culture requires mitotic activity [J].
Mortimer, I ;
Tam, P ;
MacLachlan, I ;
Graham, RW ;
Saravolac, EG ;
Joshi, PB .
GENE THERAPY, 1999, 6 (03) :403-411
[10]   Novel cationic liposomes for DNA-transfection with high efficiency and low toxicity [J].
Paukku, T ;
Lauraeus, S ;
Huhtaniemi, I ;
Kinnunen, PKJ .
CHEMISTRY AND PHYSICS OF LIPIDS, 1997, 87 (01) :23-29