The protein network of HIV budding

被引:671
作者
von Schwedler, UK
Stuchell, M
Müller, B
Ward, DM
Chung, HY
Morita, E
Wang, HE
Davis, T
He, GP
Cimbora, DM
Scott, A
Kräusslich, HG
Kaplan, J
Morham, SG
Sundquist, WI [1 ]
机构
[1] Univ Utah, Dept Biochem, Salt Lake City, UT 84132 USA
[2] Univ Utah, Dept Pathol, Salt Lake City, UT 84132 USA
[3] Univ Klinikum Heidelburg, Abt Virol, D-69120 Heidelberg, Germany
[4] Myriad Pharmaceut Inc, Salt Lake City, UT 84108 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(03)00714-1
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
HIV release requires TSG101, a cellular factor that sorts proteins into vesicles that bud into multivesicular bodies (MVB). To test whether other proteins involved in MVB biogenesis (the class E proteins) also participate in HIV release, we identified 22 candidate human class E proteins. These proteins were connected into a coherent network by 43 different protein-protein interactions, with AIP1 playing a key role in linking complexes that act early (TSG101/ESCRT-I) and late (CHMP4/ESCRT-III) in the pathway. AIP1 also binds the HIV-1 p6(Gag) and EIAV p9(Gag) proteins, indicating that it can function directly in virus budding. Human class E proteins were found in HIV-1 particles, and dominant-negative mutants of late-acting human class E proteins arrested HIV-1 budding through plasmal and endosomal membranes. These studies define a protein network required for human MVB biogenesis and indicate that the entire network participates in the release of HIV and probably many other viruses.
引用
收藏
页码:701 / 713
页数:13
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