Competitive inhibition of human immunodeficiency virus type-1 protease by the Gag-Pol transframe protein

被引:34
作者
Paulus, C
Hellebrand, S
Tessmer, U
Wolf, H
Kräusslich, HG
Wagner, R
机构
[1] Univ Regensburg, Inst Med Mikrobiol & Hyg, D-93053 Regensburg, Germany
[2] Heinrich Pette Inst Expt Virol & Immunol, D-20251 Hamburg, Germany
关键词
D O I
10.1074/jbc.274.31.21539
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
The human immunodeficiency virus type-1 (HIV-1) transframe protein p6* is located between the structural and enzymatic domains of the Gag-Pol polyprotein, Banked by the nucleocapsid (NC) and the protease (PR) domain at its amino and carboxyl termini, respectively. Here, we report that recombinant highly purified HIV-1 p6* specifically inhibits mature HIV-1 PR activity. Kinetic analyses and cross-linking experiments revealed a competitive mechanism for PR inhibition by p6*. We further demonstrate that the four carboxyl-terminal residues of p6* are essential but not sufficient for p6*-mediated inhibition of PR activity. Based on these results, we suggest a role of the transframe protein p6* in regulating HIV-1 PR activity during viral replication.
引用
收藏
页码:21539 / 21543
页数:5
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