The HIV-1 Vif PPLP motif is necessary for human APOBEC3G binding and degradation

被引:63
作者
Donahue, John P. [1 ]
Vetter, Michael L. [2 ]
Mukhtar, Nizar A. [1 ]
D'Aquila, Richard T. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Div Infect Dis, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37232 USA
关键词
HIV-1; Vif; APOBEOG; Vif PPLP motif; Vif multimerization;
D O I
10.1016/j.virol.2008.04.017
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The HIV-1 virion infectivity factor (Vif) is required during viral replication to inactivate the host cell anti-viral factor, APOBEC3G (A3G). Vif binds A3G and a Cullin5-ElonginBC E3 ubiquitin ligase complex which results in the proteasomal degradation of A3G. The Vif PPLP motif (amino acids 161-164) is essential for normal Vif function because mutations in this motif reduce the infectivity of virions produced in T-cells. In this report, we demonstrate that mutation of the Vif PPLP motif reduces Vif binding to A3G without affecting its interaction with ElonginC and Cullin5. We demonstrate that the failure of the Vif mutant to bind A3G resulted in A3G incorporation into assembling virions with loss of viral infectivity. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:49 / 53
页数:5
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