Dimerization inhibitors of HIV-1 reverse transcriptase, protease and integrase:: A single mode of inhibition for the three HIV enzymes?

被引:46
作者
Camarasa, Maria-Jose
Velazquez, Sonsoles
San-Felix, Ana
Perez-Perez, Maria-Jesus
Gago, Federico
机构
[1] CSIC, Inst Quim Med, E-28006 Madrid, Spain
[2] Univ Alcala de Henares, Dept Farmacol, Madrid 28871, Spain
关键词
HIV-1; reverse transcriptase; integrase; protease;
D O I
10.1016/j.antiviral.2006.05.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The genome of human immunodeficiency virus type 1 (HIV-1) encodes 15 distinct proteins, three of which provide essential enzymatic functions: a reverse transcriptase (RT), an integrase (IN), and a protease (PR). Since these enzymes are all homodimers, pseudohomodimers or multimers, disruption of protein-protein interactions in these retroviral enzymes may constitute an alternative way to achieve HIV-1 inhibition. A growing number. of dimerization inhibitors for these enzymes is being reported. This mini review summarizes some approaches that have been followed for the development of compounds that inhibit those three enzymes by interfering with the dimerization interfaces between the enzyme subunits. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 267
页数:8
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