Literature DB >> 12093534

Fluorescent lipid probes in the study of viral membrane fusion.

Robert Blumenthal1, Stephen A Gallo, Mathias Viard, Yossef Raviv, Anu Puri.   

Abstract

Fluorescent lipid probes are widely used in the observation of viral membrane fusion, providing a sensitive method to study fusion mechanism(s). Due to the wealth of data concerning liposome fusion, a variety of fusion assays has been designed including fluorescent probe redistribution, fluorescence dequenching, fluorescence resonance energy transfer and photosensitized labeling. These methods can be tailored for different virus fusion assays. For instance, virions can be loaded with membrane dye which dequenches at the moment of membrane merger. This allows for continuous observation of fusion and therefore kinetic information can be acquired. In the case of cells expressing viral envelope proteins, dye redistribution studies of lipidic and water-soluble fluorophores yield information about fusion intermediates. Lipid probes can be metabolically incorporated into cell membranes, allowing observation of membrane fusion in vitro with minimal chance of flip flop, non-specific transfer and formation of microcrystals. Fluorescent lipid probes have been incorporated into liposomes and/or reconstituted viral envelopes, which provide a well-defined membrane environment for fusion to occur. Interactions of the viral fusion machinery with the membrane can be observed through the photosensitized labeling of the interacting segments of envelope proteins with a hydrophobic probe. Thus, fluorescent lipid probes provide a broad repertoire of fusion assays and powerful tools to produce precise, quantitative data in real time required for the elucidation of the complex process of viral fusion.

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Year:  2002        PMID: 12093534     DOI: 10.1016/s0009-3084(02)00019-1

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  25 in total

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2.  Penetration of enveloped double-stranded RNA bacteriophages phi13 and phi6 into Pseudomonas syringae cells.

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3.  Role of endocytosis and low pH in murine hepatitis virus strain A59 cell entry.

Authors:  Patricia Eifart; Kai Ludwig; Christoph Böttcher; Cornelis A M de Haan; Peter J M Rottier; Thomas Korte; Andreas Herrmann
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4.  Viral envelope protein folding and membrane hemifusion are enhanced by the conserved loop region of HIV-1 gp41.

Authors:  Avraham Ashkenazi; Mathias Viard; Yael Wexler-Cohen; Robert Blumenthal; Yechiel Shai
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5.  Conformational changes of the HIV-1 envelope protein during membrane fusion are inhibited by the replacement of its membrane-spanning domain.

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6.  Engineered lentiviral vectors pseudotyped with a CD4 receptor and a fusogenic protein can target cells expressing HIV-1 envelope proteins.

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Journal:  Virus Res       Date:  2011-07-23       Impact factor: 3.303

7.  Detecting and Controlling Dye Effects in Single-Virus Fusion Experiments.

Authors:  Robert J Rawle; Ana M Villamil Giraldo; Steven G Boxer; Peter M Kasson
Journal:  Biophys J       Date:  2019-07-02       Impact factor: 4.033

8.  Multiphasic effects of cholesterol on influenza fusion kinetics reflect multiple mechanistic roles.

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Journal:  Biophys J       Date:  2013-09-17       Impact factor: 4.033

Review 9.  HIV entry and envelope glycoprotein-mediated fusion.

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Journal:  J Biol Chem       Date:  2012-10-05       Impact factor: 5.157

10.  Single-virus fusion experiments reveal proton influx into vaccinia virions and hemifusion lag times.

Authors:  Florian I Schmidt; Phillip Kuhn; Tom Robinson; Jason Mercer; Petra S Dittrich
Journal:  Biophys J       Date:  2013-07-16       Impact factor: 4.033

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