Enhancement of phage-mediated gene transfer by nuclear localization signal

被引:17
作者
Akuta, T
Eguchi, A
Okuyama, H
Senda, T
Inokuchi, H
Suzuki, Y
Nagoshi, E
Mizuguchi, H
Hayakawa, T
Takeda, K
Hasegawa, M
Nakanishi, M [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Gene Funct Res Lab, Tsukuba, Ibaraki 3058562, Japan
[2] DNAVEC Res Inc, Tsukuba, Ibaraki 3050856, Japan
[3] Japan Soc Promot Sci, Chiyoda Ku, Tokyo 1028471, Japan
[4] Fujita Hlth Univ, Dept Anat 1, Sch Med, Aichi 4701192, Japan
[5] Kyoto Univ, Dept Biophys, Grad Sch Sci, Sakyo Ku, Kyoto 6068502, Japan
[6] Univ Geneva, Dept Mol Biol, Geneva, Switzerland
[7] Natl Inst Hlth Sci, Dept Biochem & Biol, Setagaya Ku, Tokyo 1588501, Japan
关键词
nuclear localization signal; lambda phage; non-viral vector; gene transfer;
D O I
10.1016/S0006-291X(02)02282-9
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
The cell membrane and the nuclear membrane are two major barriers hindering the free movement of various macromolecules through animal cells. Nevertheless, some proteins can actively bypass these barriers by dint of intrinsic peptidic signals, so incorporation of these signals might improve the efficacy of artificial gene delivery vehicles. We examined the role of the nuclear localization signal (NLS) in gene transfer, using recombinant, phage as a model of the polymer/DNA complexes. We prepared a. phage displaying a 32-mer NLS of SV40 T antigen on its surface (NLS phage), and found that this NLS phage, delivered into the cytoplasm by appropriate devices, has higher affinity for the nucleus and induces the expression of encapsulated marker genes more efficiently than does the wild-type phage. This suggests that the 32-mer NLS peptide will become a practical tool for artificial gene delivery vehicles with enhanced nuclear targeting activity. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:779 / 786
页数:8
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