DNA nanoparticles and development of DNA delivery vehicles for gene therapy

被引:314
作者
Vijayanathan, V
Thomas, T
Thomas, TJ
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Med, New Brunswick, NJ 08903 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Environm & Community Med, New Brunswick, NJ 08903 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Inst Occupat Hlth Sci, New Brunswick, NJ 08903 USA
[4] Canc Inst New Jersey, New Brunswick, NJ 08903 USA
关键词
D O I
10.1021/bi0203987
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
DNA transport through the cell membrane is an essential requirement for gene therapy, which utilizes oligonucleotides and plasmid DNA. However, membrane transport of DNA is an inefficient process, and the mechanism(s) by which this process occurs is not clear. Although viral vectors are effective in gene therapy, the immune response elicited by viral proteins poses a major problem. Therefore, several laboratories are involved in the development of nonviral DNA delivery vehicles. These vehicles include polyamines, polycationic lipids, and neutral polymers, capable of condensing DNA to nanoparticles with radii of 20-100 nm. Although the structural and energetic forces involved in DNA condensation have been studied by physical biochemists for the past 25 years, this area has experienced a resurgence of interest in recent years because of the influx of biotechnologists involved in developing gene therapy protocols to combat a variety of human diseases. Despite an intense effort to study the mechanism(s) of DNA condensation using a variety of microscopic, light scattering, fluorescence, and calorimetric techniques, the precise details of the energetics of DNA nanciparticle formation and their packing assembly are not known at present. Future studies aimed at defining the mechanism(s) of DNA compaction and structural features of DNA nanoparticles might aid in the development of novel gene delivery vehicles.
引用
收藏
页码:14085 / 14094
页数:10
相关论文
共 144 条
[41]   Poly(ethylenimine) and its role in gene delivery [J].
Godbey, WT ;
Wu, KK ;
Mikos, AG .
JOURNAL OF CONTROLLED RELEASE, 1999, 60 (2-3) :149-160
[42]   Tracking the intracellular path of poly(ethylenimine)/DNA complexes for gene delivery [J].
Godbey, WT ;
Wu, KK ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5177-5181
[43]   DNA toroids: Stages in condensation [J].
Golan, R ;
Pietrasanta, LI ;
Hsieh, W ;
Hansma, HG .
BIOCHEMISTRY, 1999, 38 (42) :14069-14076
[44]   Nuclear protein import [J].
Gorlich, D .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (03) :412-419
[45]   Efficient gene transfer using reversibly cross-linked low molecular weight polyethylenimine [J].
Gosselin, MA ;
Guo, WJ ;
Lee, RJ .
BIOCONJUGATE CHEMISTRY, 2001, 12 (06) :989-994
[46]  
GOTTSCHALK S, 1994, GENE THER, V1, P185
[47]   Effect of non-pairwise-additive interactions on bundles of rodlike polyelectrolytes [J].
Ha, BY ;
Liu, AJ .
PHYSICAL REVIEW LETTERS, 1998, 81 (05) :1011-1014
[48]  
HAGERMAN PJ, 1988, ANNU REV BIOPHYS BIO, V17, P265
[49]  
He SQ, 2000, BIOPOLYMERS, V53, P329
[50]   EVIDENCE FOR TARGETED GENE-TRANSFER BY RECEPTOR-MEDIATED ENDOCYTOSIS - STABLE EXPRESSION FOLLOWING INSULIN-DIRECTED ENTRY OF NEO INTO HEPG2 CELLS [J].
HUCKETT, B ;
ARIATTI, M ;
HAWTREY, AO .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (02) :253-263