共 34 条
Exposure of the membrane-proximal external region of HIV-1 gp41 in the course of HIV-1 envelope glycoprotein-mediated fusion
被引:79
作者:

Dimitrov, Antony S.
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA

Jacobs, Amy
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA

Finnegan, Catherine M.
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h-index: 0
机构: NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA

Stiegler, Gabriela
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA

Katinger, Hermann
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA

Blumenthal, Robert
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h-index: 0
机构:
NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA
机构:
[1] NCI, Ctr Canc Res, Nanobiol Program, NIH, Frederick, MD 21702 USA
[2] Univ Nat Resources & Appl Life Sci Vienna, Inst Appl Microbiol, Vienna, Austria
关键词:
D O I:
10.1021/bi062245f
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 membrane-proximal external region (MPER) of HIV-1 gp41 is highly conserved and critical for the fusogenic ability of the virus. However, little is known about the activity of this region in the context of viral fusion. In this study we investigate the temporal exposure of MPER during the course of HIV-1 Env-mediated fusion. We employed the broadly neutralizing monoclonal antibodies 2F5 and 4E10, whose epitopes localize to this region as indicators for accessibility to this region. Time of addition experiments indicated that escape of HIV-1 infection inhibition by 2F5 and 4E10 occurred concomitantly with that of C34, a peptide that blocks the six-helix bundle formation and fusion, which was about 20 min later than escape of inhibition by the mAb b12 that blocks CD4-gp120 attachment. We also probed accessibility of the MPER region on fusion intermediates by measuring the binding of the monoclonal antibodies at different time points during the fusion reaction. Immunofluorescence and in-cell Western assays showed that binding of 2F5 and 4E10 decreased upon triggering HIV-1 Env-expressing cells with appropriate target cells. Addition of C34 did not counteract the loss of antibody binding, suggesting that changes in exposure of MPER occur independently of six-helix bundle formation.
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页码:1398 / 1401
页数:4
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