Identification of a novel type of small molecule inhibitor against HIV-1

被引:5
|
作者
Kim, Byung Soo [1 ]
Park, Jung Ae [1 ]
Kim, Min-Jung [1 ]
Kim, Seon Hee [2 ]
Yu, Kyung Lee [2 ]
You, Ji Chang [1 ,2 ]
机构
[1] Avixgen Inc, Seoul 137701, South Korea
[2] Catholic Univ Korea, Sch Med, Dept Pathol, Natl Res Lab Mol Virol, Seoul 137701, South Korea
基金
新加坡国家研究基金会;
关键词
HIV-1; inhibitor; Infectivity; Novel chemical structure; Reverse transcription; Viral protein processing; ANTI-HIV; PROGRESS;
D O I
10.5483/BMBRep.2015.48.2.239
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
Here we report a new chemical inhibitor against HIV-1 with a novel structure and mode of action. The inhibitor, designated as A1836, inhibited HIV-1 replication and virus production with a 50% inhibitory concentration (IC50) of 2.0 mu M in an MT-4 cell-based and cytopathic protection antiviral assay, while its 50% cytotoxic concentration (CC50) was much higher than 50 mu M. Examination of the effect of A1836 on in vitro HIV-1 reverse transcriptase (RT) and integrase showed that neither were molecular targets of A1836. The characterization and re-infection assay of the HIV-1 virions generated in the presence of A1836 showed that the synthesis of early RT products in the cells infected with the virions was inhibited dose-dependently, due in part to abnormal protein formation within the virions, thus resulting in an impaired infectivity. These results suggest that A1836 might be a novel candidate for the development of a new type of HIV-1 inhibitor.
引用
收藏
页码:121 / 126
页数:6
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