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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
来源:
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.
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页码:121 / 126
页数:6
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