Protein stability influences human immunodeficiency virus type 2 Vpr virion incorporation and cell cycle effect

被引:33
作者
Kewalramani, VN
Park, CS
Gallombardo, PA
Emerman, M
机构
[1] FRED HUTCHINSON CANC RES CTR,DIV MOLEC MED,SEATTLE,WA 98104
[2] FRED HUTCHINSON CANC RES CTR,DIV BASIC SCI,SEATTLE,WA 98104
[3] UNIV WASHINGTON,PROGRAM MOLEC & CELLULAR BIOL,SEATTLE,WA 98195
[4] UNIV WASHINGTON,DEPT MICROBIOL,SEATTLE,WA 98195
关键词
D O I
10.1006/viro.1996.0201
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Using recombinant proteins as standards, we calculated the amount of Vpr and Vpx present in HIV-2(ROD) particles. We find 2000-3000 copies of Vpx per particle but only 40-50 copies of Vpr. We investigated the reasons for this discrepancy between Vpx and Vpr and found that viral factors, including HIV-2 Vpx, do not restrict its incorporation. Instead, the accumulation of HIV-2(ROD) Vpr during infection is restricted by a short protein half-life which acts to limit its virion incorporation. The half-life of HIV-2 Vpr was calculated to be about 90 min, while HIV-2 Vpx and HIV-1 Vpr had half-lifes of 36 and 20 hr, respectively. Moreover, while both HIV-1 Vpr and HIV-2 Vpr cause cells to accumulate in G2 of the cell cycle, the effect of HIV-2 Vpr is attenuated relative to HIV-1 Vpr. Thus, protein stability correlates with both the function of Vpr and its Virion incorporation. (C) 1996 Academic Press, Inc.
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收藏
页码:326 / 334
页数:9
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