Green fluorescent protein (GFP) fusion constructs in gene therapy research

被引:66
作者
Wahlfors, J [1 ]
Loimas, S [1 ]
Pasanen, T [1 ]
Hakkarainen, T [1 ]
机构
[1] Univ Kuopio, AI Virtanen Inst Mol Sci, Gen Transfer Technol Grp, Kuopio 70211, Finland
基金
芬兰科学院;
关键词
gene therapy; GFP fusion protein;
D O I
10.1007/s004180000219
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The history of green fluorescent protein (GFP) as a marker is less than 10 years old, but it has already made a major impact on many areas of natural sciences, especially on cell biology and histochemistry. GFP can be detected in living cells without selection or staining and it can be fused to other proteins to yield fluorescent chimeras. The potential of GFP has also been recognised by gene therapy researchers and various GFP-tagged therapeutic proteins have been constructed. These chimeric proteins have been used to determine the expression level, site and time course of the therapeutic gene, or the correlation between gene transfer rate and therapeutic outcome. This review summarises the status of the applications of GFP fusions in gene therapy research.
引用
收藏
页码:59 / 65
页数:7
相关论文
共 49 条
[1]  
Aints A, 1999, J GENE MED, V1, P275
[2]   Polyethylene glycol-mediated infection of non-permissive mammalian cells with semliki forest virus: application to signal transduction studies [J].
Arudchandran, R ;
Brown, MJ ;
Song, JS ;
Wank, SA ;
Haleem-Smith, H ;
Rivera, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 222 (1-2) :197-208
[3]   Evaluation of VP22 spread in tissue culture [J].
Brewis, N ;
Phelan, A ;
Webb, J ;
Drew, J ;
Elliott, G ;
O'Hare, P .
JOURNAL OF VIROLOGY, 2000, 74 (02) :1051-1056
[4]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[5]  
Degreve B, 1998, J VIROL, V72, P9535
[6]   The N-terminal matrix domain of HIV-1 gag is sufficient but not necessary for viral protein U-mediated enhancement of particle release through a membrane-targeting mechanism [J].
Deora, A ;
Spearman, P ;
Ratner, L .
VIROLOGY, 2000, 269 (02) :305-312
[7]   Intercellular delivery of thymidine kinase prodrug activating enzyme by the herpes simplex virus protein, VP22 [J].
Dilber, MS ;
Phelan, A ;
Aints, A ;
Mohamed, AJ ;
Elliott, G ;
Smith, CIE ;
O'Hare, P .
GENE THERAPY, 1999, 6 (01) :12-21
[8]   Intercellular trafficking and protein delivery by a herpesvirus structural protein [J].
Elliott, G ;
OHare, P .
CELL, 1997, 88 (02) :223-233
[9]   Cytoplasm-to-nucleus translocation of a herpesvirus tegument protein during cell division [J].
Elliott, G ;
O'Hare, P .
JOURNAL OF VIROLOGY, 2000, 74 (05) :2131-2141
[10]   Live-cell analysis of a green fluorescent protein-tagged herpes simplex virus infection [J].
Elliott, G ;
O'Hare, P .
JOURNAL OF VIROLOGY, 1999, 73 (05) :4110-4119