Plasma membrane is the site of productive HIV-1 particle assembly
被引:276
作者:
Jouvenet, Nolwenn
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Jouvenet, Nolwenn
Neil, Stuart J. D.
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Neil, Stuart J. D.
Bess, Cameron
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Bess, Cameron
Johnson, Marc C.
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Johnson, Marc C.
Virgen, Cesar A.
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Virgen, Cesar A.
Simon, Sanford M.
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Simon, Sanford M.
Bieniasz, Paul D.
论文数: 0引用数: 0
h-index: 0
机构:Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
Bieniasz, Paul D.
机构:
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10021 USA
[2] Rockefeller Univ, Lab Retrovirol, New York, NY 10021 USA
[3] Rockefeller Univ, Lab Cellular Biophys, New York, NY 10021 USA
[4] Univ Missouri, Dept Mol Microbiol & Immunol, Columbia, MO 65211 USA
来源:
PLOS BIOLOGY
|
2006年
/
4卷
/
12期
关键词:
D O I:
10.1371/journal.pbio.0040435
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:
Recently proposed models that have gained wide acceptance posit that HIV-1 virion morphogenesis is initiated by targeting the major structural protein (Gag) to late endosomal membranes. Thereafter, late endosome-based secretory pathways are thought to deliver Gag or assembled virions to the plasma membrane (PM) and extracellular milieu. We present several findings that are inconsistent with this model. Specifically, we demonstrate that HIV-1 Gag is delivered to the PM, and virions are efficiently released into the extracellular medium, when late endosome motility is abolished. Furthermore, we show that HIV-1 virions are efficiently released when assembly is rationally targeted to the PM, but not when targeted to late endosomes. Recently synthesized Gag first accumulates and assembles at the PM, but a proportion is subsequently internalized via endocytosis or phagocytosis, thus accounting for observations of endosomal localization. We conclude that HIV-1 assembly is initiated and completed at the PM, and not at endosomal membranes.