Multifaceted action of Fuzeon as virus-cell membrane fusion inhibitor

被引:43
|
作者
Ashkenazi, Avraham [1 ]
Wexler-Cohen, Yael [1 ]
Shai, Yechiel [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2011年 / 1808卷 / 10期
基金
以色列科学基金会;
关键词
HIV entry inhibitor; Membrane fusion; Viral envelope protein; Transmembrane protein; HIV-1 ENVELOPE GLYCOPROTEIN; TYPE-1; GP41; ENTRY INHIBITORS; HEPTAD REPEAT; MULTIFUNCTIONAL DOMAINS; PEPTIDE INHIBITOR; POTENT INHIBITORS; SYNTHETIC PEPTIDE; HELICAL DOMAIN; ANTIBODY; 2F5;
D O I
10.1016/j.bbamem.2011.06.020
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 viral peptide fusion inhibitor Fuzeon (T-20/DP178/enfuvirtide) is an essential part of the drug combination that has significantly increased the quality of life and life span of many acquired immunodeficiency syndrome (AIDS) patients. Its development as a drug preceded the elucidation of its precise inhibitory mechanism, as well as its molecular targets. The initial model was that Fuzeon inhibits human immunodeficiency virus (HIV) entry by targeting one site within the viral transmembrane envelope protein. Herein, we describe the emerging discoveries that extend this model towards a multifaceted mechanism for the drug in targeting HIV. This significantly advances the understanding of how viruses enter host cells and opens a new window of opportunity for designing future viral fusion inhibitors. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2352 / 2358
页数:7
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