Intracellular localization of Herpes simplex virus type 1 thymidine kinase fused to different fluorescent proteins depends on choice of fluorescent tag

被引:21
作者
Söling, A
Simm, A
Rainov, NG
机构
[1] Univ Halle Wittenberg, Mol Neurooncol Lab, Dept Neurosurg, D-06097 Halle Saale, Germany
[2] Univ Halle Wittenberg, Dept Cardiothorac Surg, D-06097 Halle Saale, Germany
[3] Univ Liverpool, Dept Neurol Sci, Liverpool 9L 7LJ, Merseyside, England
关键词
brain tumor; gene therapy; red fluorescent protein; green fluorescent protein; Herpes simplex virus type 1 thymidine kinase;
D O I
10.1016/S0014-5793(02)03201-5
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
Gene therapy employing the suicide gene/prodrug activating system Herpes simplex virus type 1 thymidine kinase (HSV-TK)/ganciclovir (GCV) is effective in killing malignant tumor cells. Labeling of the HSV-TK enzyme with fluorescent proteins makes possible the non-invasive imaging of transduction efficiency, enzyme localization and activity in cell culture and in animal models of human cancers. Here we report the expression of HSV-TK tagged with different fluorescent proteins (EGFP, DSRed1, DsRed2, dsdrFP616) and show that intracellular localization of the fusion products depends on the nature of the fluorescent tag despite the presence of several nuclear targeting signals within the enzyme itself. Coexpression of red fluorescent HSV-TK fusion proteins with TK-EGFP or untagged HSV-TK allowed these proteins to enter the nucleus by inhibiting formation of red fluorescent protein oligomers. As enzyme localization may influence HSV-TK activity, this observation is of potential importance to gene therapy studies. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 158
页数:6
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