Biophysical and structural characterization of polyethylenimine-mediated siRNA delivery in vitro

被引:283
作者
Grayson, Amy C. Richards
Doody, Anne M.
Putnam, David
机构
[1] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Sch Chem & Biomol Engn, Ithaca, NY 14853 USA
关键词
luciferases; polyethylenimine; RNA interference; small interfering RNA; transfection;
D O I
10.1007/s11095-006-9009-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. The goals of this study were as follows: 1) to evaluate the efficacy of different polyethylenimine (PEI) structures for siRNA delivery in a model system, and 2) to determine the biophysical and structural characteristics of PEI that relate to siRNA delivery. Materials and Methods. Biophysical characterization (effective diameter and zeta potential), cytotoxicities, relative binding affinities and in vitro transfection efficiencies were determined using nanocomplexes formed from PEI's of 800, 25,000, (both branched) and 22,000 (linear) molecular weights at varying N:P ratios and siRNA concentrations. The HR5-CL11 cell line stably expressing luciferase was used as a model system in vitro. Results. Successful siRNA delivery was observed within a very narrow window of conditions, and only with the 25,000 branched PEI at an N:P ratio of 6:1 and 8:1 and with 200 nM siRNA. While the zeta potential and size of PEI:siRNA complexes correlated to transfection efficacy in some cases, complex stability may also affect transfection efficacy. Conclusions. The ability of PEI to transfer functionally active siRNA to cells in culture is surprisingly dependent on its biophysical and structural characteristics when compared to its relative success and ease of use for DNA delivery.
引用
收藏
页码:1868 / 1876
页数:9
相关论文
共 51 条
[1]   Delivery of unmodified bioactive ribozymes by an RNA-stabilizing polyethylenimine (LMW-PEI) efficiently down-regulates gene expression [J].
Aigner, A ;
Fischer, D ;
Merdan, T ;
Brus, C ;
Kissel, T ;
Czubayko, F .
GENE THERAPY, 2002, 9 (24) :1700-1707
[2]   Exploring polyethylenimine-mediated DNA transfection and the proton sponge hypothesis [J].
Akinc, A ;
Thomas, M ;
Klibanov, AM ;
Langer, R .
JOURNAL OF GENE MEDICINE, 2005, 7 (05) :657-663
[3]  
Behr JP, 1997, CHIMIA, V51, P34
[4]  
Bishop NE, 1997, REV MED VIROL, V7, P199, DOI 10.1002/(SICI)1099-1654(199712)7:4<199::AID-RMV203>3.0.CO
[5]  
2-F
[6]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[7]   Synthesis of linear polyethylenimine derivatives for DNA transfection [J].
Brissault, B ;
Kichler, A ;
Guis, C ;
Leborgne, C ;
Danos, O ;
Cheradame, H .
BIOCONJUGATE CHEMISTRY, 2003, 14 (03) :581-587
[8]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[9]   Biophysical characterization of PEI/DNA complexes [J].
Choosakoonkriang, S ;
Lobo, BA ;
Koe, GS ;
Koe, JG ;
Middaugh, CR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (08) :1710-1722
[10]   Polyethylenimine but not cationic lipid improves antisense activity of 3'-capped phosphodiester oligonucleolides [J].
Dheur, S ;
Dias, N ;
Van Aerschot, A ;
Herdewijn, P ;
Bettinger, T ;
Rémy, JS ;
Hélène, C ;
Saison-Behmoaras, ET .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1999, 9 (06) :515-525