机构:
Aaron Diamond AIDS Res Ctr, Howard Hughes Med Inst, New York, NY 10016 USA
Rockefeller Univ, Lab Retrovirol, New York, NY 10065 USAAaron Diamond AIDS Res Ctr, Howard Hughes Med Inst, New York, NY 10016 USA
Bieniasz, Paul D.
[1
,2
]
机构:
[1] Aaron Diamond AIDS Res Ctr, Howard Hughes Med Inst, New York, NY 10016 USA
[2] Rockefeller Univ, Lab Retrovirol, New York, NY 10065 USA
VIRUS TYPE-1 GAG;
ESCRT-III COMPLEX;
PLASMA-MEMBRANE;
VPU PROTEIN;
MATRIX PROTEIN;
PARTICLE RELEASE;
STRUCTURAL BASIS;
INHIBITS HIV-1;
LIVING CELLS;
LIVE CELLS;
D O I:
10.1016/j.chom.2009.05.015
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Recent work has illuminated three critical aspects of the cell biology of HIV-1 particle genesis. First, we have come to understand which cellular membranes are selected as platforms for virus particle assembly and how this occurs. Second, an understanding of how the host ESCRT pathway enables virion budding is accruing. Third, it has become apparent that a host inhibitor can block HIV-1 particle release and that antagonism of this inhibitor underlies the ability of HIV and SIV accessory genes to facilitate particle release. Here, I review recent progress in these three areas.
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页码:550 / 558
页数:9
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