Novel polyamine-dialkyl phosphate conjugates for gene carriers. Facile synthetic route via an unprecedented dialkyl phosphate

被引:19
作者
Dewa, T [1 ]
Ieda, Y
Morita, K
Wang, L
MacDonald, RC
Iida, K
Yamashita, K
Oku, N
Nango, M
机构
[1] Nagoya Inst Technol, Showa Ku, Nagoya, Aichi 4668555, Japan
[2] Northwestern Univ, PRESTO, JST, Dept Biochem Mol Biol & Cell Biol, Evanston, IL 60208 USA
[3] Nagoya Municipal Ind Res Inst, Atsuta Ku, Nagoya, Aichi 4560058, Japan
[4] Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, Shizuoka, Japan
[5] Univ Shizuoka, Sch Pharmaceut Sci, COE Program 21st Century, Shizuoka, Japan
关键词
D O I
10.1021/bc049925k
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To develop a novel nonviral gene carrier, three types of polyamine-dialky phosphates conjugates were synthesized via an unprecedented synthetic intermediate, dimerized dicetyl phosphate (DCP) anhydride, and the transfection efficiency and the complexation properties of the conjugate-DNA were evaluated. Condensation of DCP by 1,3,5-triisopropylbenzenesulfonyl chloride, TPSCI, gives the dimerized anhydride, which is stable enough to isolate by column chromatography in similar to90% yield. The anhydride is reactive with various amines, i.e., spermidine, spermine, and polyethylenimine (PEI-(1800)), providing corresponding polyamine-DCP conjugates via phosphoramidate linkage. The polyamine-DCP conjugates exhibited moderate transfection efficacy evaluated by P-galactosidase assay. The conjugate-DNA complex was observed by using an atomic force microscope (AFM), revealing that the PEI(1800)-DCP conjugate, which showed the most efficient transfection, enables the formation of the more compact complex with DNA.
引用
收藏
页码:824 / 830
页数:7
相关论文
共 26 条
[1]   GENE-TRANSFER WITH SYNTHETIC CATIONIC AMPHIPHILES - PROSPECTS FOR GENE-THERAPY [J].
BEHR, JP .
BIOCONJUGATE CHEMISTRY, 1994, 5 (05) :382-389
[2]   PLATELET-INDUCED VASCULAR SMOOTH-MUSCLE CELL-PROLIFERATION IS MODULATED BY THE GROWTH AMPLIFICATION FACTORS SEROTONIN AND ADENOSINE-DIPHOSPHATE [J].
CROWLEY, ST ;
DEMPSEY, EC ;
HORWITZ, KB ;
HORWITZ, LD .
CIRCULATION, 1994, 90 (04) :1908-1918
[3]   ON THE MECHANISM OF REACTION OF ACTIVATED PHOSPHORYL COMPOUNDS WITH PHOSPHORYL ANIONS - A REASSESSMENT OF THE ROLE OF DIOXADIPHOSPHETANES [J].
CULLIS, PM ;
KAYE, AD ;
TRIPPETT, S .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (19) :1464-1466
[4]   Intracellular control of gene trafficking using liposomes as drug carriers [J].
Harashima, H ;
Shinohara, Y ;
Kiwada, H .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (01) :85-89
[5]   Gene therapy [J].
Kay, MA ;
Liu, DX ;
Hoogerbrugge, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (24) :12744-12746
[6]   Factors governing the assembly of cationic phospholipid-DNA complexes [J].
Kennedy, MT ;
Pozharski, EV ;
Rakhmanova, VA ;
MacDonald, RC .
BIOPHYSICAL JOURNAL, 2000, 78 (03) :1620-1633
[7]   Influence of membrane-active peptides on lipospermine/DNA complex mediated gene transfer [J].
Kickler, A ;
Mechtler, K ;
Behr, JP ;
Wagner, E .
BIOCONJUGATE CHEMISTRY, 1997, 8 (02) :213-221
[8]   Mixtures of cationic lipid O-ethylphosphatidylcholine with membrane lipids and DNA:: Phase diagrams [J].
Koynova, R ;
MacDonald, RC .
BIOPHYSICAL JOURNAL, 2003, 85 (04) :2449-2465
[9]  
LASIC DD, 1997, LIPOSOMES GENE DELIV
[10]   Physical and biological properties of cationic triesters of phosphatidylcholine [J].
MacDonald, RC ;
Ashley, GW ;
Shida, MM ;
Rakhmanova, VA ;
Tarahovsky, YS ;
Pantazatos, DP ;
Kennedy, MT ;
Pozharski, EV ;
Baker, KA ;
Jones, RD ;
Rosenzweig, HS ;
Choi, KL ;
Qiu, RZ ;
McIntosh, TJ .
BIOPHYSICAL JOURNAL, 1999, 77 (05) :2612-2629