HIV-1 Reverse Transcriptase: A therapeutical target in the spotlight

被引:54
|
作者
Castro, HC
Loureiro, NIV
Pujol-Luz, M
Souza, AMT
Albuquerque, MG
Santos, DO
Cabral, LM
Frugulhetti, IC
Rodrigues, CR
机构
[1] Univ Fed Fluminense, Dept Biol Celular & Mol, IB, Lab Bioquim & Modelagem Mol LaBioMol, BR-24001970 Niteroi, RJ, Brazil
[2] Univ Fed Rio de Janeiro, Dept Quim Organ, IQ, Lab Modelagem Mol LabMMol, BR-21949900 Rio De Janeiro, Brazil
[3] Univ Fed Fluminense, Dept Biol Celular & Mol, IB, Mol Virol Lab, BR-24001970 Niteroi, RJ, Brazil
[4] Univ Fed Rio de Janeiro, Fac Farm, DLab Modelagem Mol & QSAR ModMolQSAR, BR-21941590 Rio De Janeiro, Brazil
关键词
reverse transcriptase; nucleoside; nucleotide; non-nucleoside; DNA; RNA; antiretroviral; AIDS;
D O I
10.2174/092986706775476089
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
Human Immunodeficiency Virus type 1 Reverse Transcriptase (HIV-1 RT) is one of the most important targets for treatment of Acquired Immune Deficiency Syndrome (AIDS). It catalyzes the reverse transcription of HIV-RNA into a double stranded DNA, and the knowledge of its substrate specificity and catalytic mechanism has guided the development of several inhibitors widely used on current HIV/AIDS therapy. However, mutations in HIV-1 RT structure can lead to the emergence of drug-resistant virus strains. The goal of this review is to summarize relevant structural features of HIV-1 RT and its inhibitors in such a way that this cost-effective target in the development of new antiretroviral drugs is particularly highlighted.
引用
收藏
页码:313 / 324
页数:12
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