Identification of Human Immunodeficiency Virus Type-1 Gag-TSG101 Interaction Inhibitors by High-throughput Screening
Overview
Authors
Affiliations
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.
BK Polyomavirus Hijacks Extracellular Vesicles for Transmission.
Handala L, Blanchard E, Raynal P, Roingeard P, Morel V, Descamps V J Virol. 2020; 94(6).
PMID: 31896595 PMC: 7158717. DOI: 10.1128/JVI.01834-19.
Dendritic Cells, the Double Agent in the War Against HIV-1.
Martin-Moreno A, Munoz-Fernandez M Front Immunol. 2019; 10:2485.
PMID: 31708924 PMC: 6820366. DOI: 10.3389/fimmu.2019.02485.
Hoffman H, Fernandez M, Groves N, Freed E, van Engelenburg S J Biol Chem. 2019; 294(44):16266-16281.
PMID: 31519756 PMC: 6827313. DOI: 10.1074/jbc.RA119.009372.