Double-labelled HIV-1 particles for study of virus-cell interaction

被引:106
作者
Lampe, Marko
Briggs, John A. G.
Endress, Thomas
Glass, Baerbel
Riegelsberger, Stefan
Kraeusslich, Hans-Georg
Lamb, Don C.
Braeuchle, Christoph
Mueller, Barbara
机构
[1] Univ Klinikum Heidelberg, Dept Virol, D-69120 Heidelberg, Germany
[2] Univ Munich, Dept Chem & Biochem, D-81377 Munich, Germany
[3] Univ Munich, Ctr NanoSci, D-80539 Munich, Germany
[4] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
关键词
HIV-1; single virus tracing; virus entry; fluorescence labelling; heparan sulfate;
D O I
10.1016/j.virol.2006.10.005
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Human immunodeficiency virus (HIV) delivers its genome to a host cell through fusion of the viral envelope with a cellular membrane. While the viral and cellular proteins involved in entry have been analyzed in detail, the dynamics of virus-cell fusion are largely unknown. Single virus tracing (SVT) provides the unique opportunity to visualize viral particles in real time allowing direct observation of the dynamics of this stochastic process. For this purpose, we developed a double-coloured HIV derivative carrying a green fluorescent label attached to the viral matrix protein combined with a red label fused to the viral Vpr protein designed to distinguish between complete virions and subviral particles lacking MA after membrane fusion. We present here a detailed characterization of this novel tool together with exemplary live cell imaging studies, demonstrating its suitability for real-time analyses of HIV-cell interaction. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:92 / 104
页数:13
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