A new class of HIV-1 inhibitors and the target identification via proteomic profiling

Autor: Hu Zhou, Xiao-Jing Yuan, Mark A. Wainberg, Jian-Min Yue, Ying-Zi Ge, Yechun Xu, Bin Zhou, Ruo-Xuan Xiao, Ying-Shan Han
Rok vydání: 2018
Předmět:
Zdroj: Science China Chemistry. 61:1430-1439
ISSN: 1869-1870
1674-7291
DOI: 10.1007/s11426-018-9283-3
Popis: Anti-HIV screening with the MT-4/MTT assay on a focused library of structurally diverse natural products has led to the discovery of a group of steroids with potent activities, which include four new ergostane-type steroids, named amotsterols A-D (1-4), together with two known analogs. Among them, the most potent amotsterol D (4) exhibited anti-HIV activity against wildtype and some clinically relevant multidrug resistant HIV-1 strains. Subsequent studies on its target identification through a proteomic approach found that compound 4 might target PKM2, a rate limiting enzyme of glycolysis, in host cells to restrict HIV replication. The docking model of compound 4 to PKM2 showed that the two hydroxyl groups of 4 form hydrogen bonds with the two parallel Y390 in each subunit of PKM2 separately, and the ring C of 4 is sandwiched between the two parallel aromatic rings of F26. The identified hit compound may have the potential to be further developed as a novel anti-HIV agent. These results demonstrated that an integrated approach, which combines new chemical structures and phenotypic screening with a proteomic approach, could not only identify novel HIV-1 inhibitors, but also elucidate the unknown targets of compound interactions in antiviral drug discovery.
Databáze: OpenAIRE
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