ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly

被引:26
作者
Ku, Pei-I [1 ]
Bendjennat, Mourad [1 ]
Ballew, Jeff [1 ]
Landesman, Michael B. [1 ]
Saffarian, Saveez [1 ,2 ,3 ]
机构
[1] Univ Utah, Dept Phys & Astron, Salt Lake City, UT 84112 USA
[2] Univ Utah, Ctr Cell & Genome Sci, Salt Lake City, UT USA
[3] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
基金
美国国家科学基金会;
关键词
LATE-DOMAIN; ESCRT-III; HELICAL STRUCTURES; STRUCTURAL BASIS; BINDING PARTNER; BRO1; DOMAIN; IN-VITRO; PROTEIN; UBIQUITIN; RELEASE;
D O I
10.1371/journal.pone.0096950
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polymerization of Gag on the inner leaflet of the plasma membrane drives the assembly of Human Immunodeficiency Virus 1 (HIV-1). Gag recruits components of the endosomal sorting complexes required for transport (ESCRT) to facilitate membrane fission and virion release. ESCRT assembly is initiated by recruitment of ALIX and TSG101/ESCRT-I, which bind directly to the viral Gag protein and then recruit the downstream ESCRT-III and VPS4 factors to complete the budding process. In contrast to previous models, we show that ALIX is recruited transiently at the end of Gag assembly, and that most ALIX molecules are recycled into the cytosol as the virus buds, although a subset remains within the virion. Our experiments imply that ALIX is recruited to the neck of the assembling virion and is mostly recycled after virion release.
引用
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页数:8
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