| Literature DB >> 26192705 |
Liang Xu1, Tao Zhang1, Xiaoyu Xu1, Huihui Chong2, Wenqing Lai1, Xifeng Jiang1, Chao Wang1, Yuxian He2, Keliang Liu1.
Abstract
DNA triplexes with hydrophobic modifications were designed and evaluated for their activity as inhibitors of the cell fusion of human immunodeficiency virus type 1 (HIV-1). Triplex inhibitors displayed low micromolar activities in the cell-cell fusion assay and nanomolar activities in the anti-HIV-1 pseudovirus test. Helix structure and the presence of sufficient numbers of hydrophobic regions were essential for the antifusion activity. Results from native polyacrylamide gel electrophoresis and a fluorescent resonance energy transfer-based inhibitory assay indicated that these triplexes may interact with the primary pocket at the glycoprotein 41 (gp41) N-heptad repeat, thereby inhibiting formation of the HIV-1 gp41 6-helical bundle. Triplex-based complexes may represent a novel category of HIV-1 inhibitors in anti-HIV-1 drug discovery.Entities:
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Year: 2015 PMID: 26192705 PMCID: PMC4507350 DOI: 10.1089/nat.2015.0535
Source DB: PubMed Journal: Nucleic Acid Ther ISSN: 2159-3337 Impact factor: 5.486