The Gag precursor of HIV-1, formed of the four proteic regions matrix (MA), capsid (CA), nucleocapsid (NC) and p6, orchestrates virus morphogenesis. This complex process relies on three major interactions, NC-RNA acting as a scaffold, CA-CA and MA-membrane that targets assembly to the plasma membrane (PM). The characterization of the molecular mechanism of retroviral assembly has extensively benefited from biochemical studies and more recently an important step forward was achieved with the use of fluorescence-based techniques and fluorescently labeled viral proteins. In this review, we summarize the findings obtained with such techniques, notably quantitative-based approaches, which highlight the role of the NC region in Gag assembly. (C) 2014 Elsevier B.V. All rights reserved.
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Rockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USARockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USA
Tomasini, Michael D.
Johnson, Daniel S.
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Rockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USA
Hofstra Univ, Dept Phys & Astron, 151 Hofstra Univ, Hempstead, NY 11550 USARockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USA
Johnson, Daniel S.
Mincer, Joshua S.
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Rockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USA
Icahn Sch Med Mt Sinai, Dept Anesthesiol, New York, NY 10029 USA
Mem Sloan Kettering Canc Ctr, Dept Anestheosol & Crit Care Med, New York, NY 10021 USARockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USA
Mincer, Joshua S.
Simon, Sanford M.
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Rockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USARockefeller Univ, Lab Cellular Biophys, 1230 York Ave, New York, NY 10021 USA