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.
引用
收藏
页码:2970 / 2976
页数:7
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