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Identification of human immunodeficiency virus type-1 Gag-TSG101 interaction inhibitors by high-throughput screening
被引:5
作者:
Siarot, Lowela
[1
,2
,3
]
Chutiwitoonchai, Nopporn
[1
,2
]
Sato, Hirotaka
[1
,2
]
Chang, Hao
[1
,2
,4
]
Sato, Hironori
[5
]
Fujino, Masayuki
[6
]
Murakami, Tsutomu
[6
]
Aono, Toshihiro
[3
]
Kodama, Eiichi
[7
,8
]
Kuroda, Kazumichi
[9
]
Takei, Masami
[9
]
Aida, Yoko
[1
,2
,4
]
机构:
[1] RIKEN, Nano Med Engn Lab, Cluster Pioneering Res, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[2] RIKEN, Viral Infect Dis Unit, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[3] Univ Tokyo, Biotechnol Res Ctr, Tokyo, Japan
[4] Univ Tokyo, Grad Sch Frontier Sci, Lab Viral Infect Dis, Dept Med Genome Sci, Saitama, Japan
[5] Natl Inst Infect Dis, Pathogen Genom Ctr, Lab Viral Genom, Tokyo, Japan
[6] Natl Inst Infect Dis, AIDS Res Ctr, Tokyo, Japan
[7] Tohoku Univ, Int Inst Disaster Sci, Div Infect Dis, Sendai, Miyagi, Japan
[8] Tohoku Univ, Tohoku Med Megabank Org, Sendai, Miyagi, Japan
[9] Nihon Univ, Sch Med, Tokyo, Japan
关键词:
HIV-1;
Gag;
TSG101;
Gag-TSG101 interaction inhibitors;
inhibitor;
ELISA;
High-throughput screening;
TSG101;
INFECTION;
DOMAIN;
RELEASE;
MOTIFS;
D O I:
10.1016/j.bbrc.2018.08.079
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 interaction between viral protein Gag and cellular protein tumor susceptibility gene 101 (TSG101) is a crucial step in the HIV-1 replication cycle. This interaction initiates the viral assembly/budding via the cellular endosomal sorting complexes required for transport (ESCRT) pathway, making it a potential target for antiviral therapy. Here we developed a simple, robust, and reliable high-throughput screening (HTS) system based on enzyme-linked immunosorbent assay (ELISA) to identify compounds that inhibit HIV-1 replication by targeting Gag-TSG101 interaction. Through screening of the 9600-compound library using the established HTS system, several hit compounds, which inhibited Gag-TSG101 interaction, were identified. Subsequent assays revealed two hit compounds, HSM-9 and HSM-10, which have antiviral activity against CD4(+) T cell-tropic NL4-3 and macrophage-tropic JR-CSF HIV-1 strains. These results suggest that our established HTS system is an indispensable tool for the identification of HIV-1 Gag-TSG101 interaction inhibitors. (C) 2018 Elsevier Inc. All rights reserved.
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页码:2970 / 2976
页数:7
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