共 11 条
Green fluorescent protein-tagged retroviral envelope protein for analysis of virus-cell interactions
被引:13
作者:

Spitzer, D
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机构: German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany

Dittmar, KEJ
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机构: German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany

Rohde, M
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机构: German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany

Hauser, H
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机构:
German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany

Wirth, D
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机构: German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany
机构:
[1] German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, D-38124 Braunschweig, Germany
[2] German Res Ctr Biotechnol, Dept Microbial Pathogenesis & Vaccine Res, D-38124 Braunschweig, Germany
关键词:
D O I:
10.1128/JVI.77.10.6070-6075.2003
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Fluorescent retroviral envelope (Env) proteins were developed for direct visualization of viral particles. By fusing the enhanced green fluorescent protein (eGFP) to the N terminus of the amphotropic 4070A envelope protein, extracellular presentation of eGFP was achieved. Viruses incorporated the modified Env protein and efficiently infected cells. We used the GFP-tagged viruses for staining retrovirus receptor-positive cells, thereby circumventing indirect labeling techniques. By generating cells which conditionally expressed the GFP-tagged Env protein, we could confirm an inverse correlation between retroviral Env expression and infectivity (superinfection). eGFP-tagged virus particles are suitable for monitoring the dynamics of virus-cell interactions.
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页码:6070 / 6075
页数:6
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