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Targeting RNA–Protein Interactions within the Human Immunodeficiency Virus Type 1 Lifecycle

[Image: see text] RNA–protein interactions are vital throughout the HIV-1 life cycle for the successful production of infectious virus particles. One such essential RNA–protein interaction occurs between the full-length genomic viral RNA and the major structural protein of the virus. The initial int...

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Detalles Bibliográficos
Autores principales: Bell, Neil M., L’Hernault, Anne, Murat, Pierre, Richards, James E., Lever, Andrew M. L., Balasubramanian, Shankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928988/
https://www.ncbi.nlm.nih.gov/pubmed/24358934
http://dx.doi.org/10.1021/bi401270d
Descripción
Sumario:[Image: see text] RNA–protein interactions are vital throughout the HIV-1 life cycle for the successful production of infectious virus particles. One such essential RNA–protein interaction occurs between the full-length genomic viral RNA and the major structural protein of the virus. The initial interaction is between the Gag polyprotein and the viral RNA packaging signal (psi or Ψ), a highly conserved RNA structural element within the 5′-UTR of the HIV-1 genome, which has gained attention as a potential therapeutic target. Here, we report the application of a target-based assay to identify small molecules, which modulate the interaction between Gag and Ψ. We then demonstrate that one such molecule exhibits potent inhibitory activity in a viral replication assay. The mode of binding of the lead molecules to the RNA target was characterized by (1)H NMR spectroscopy.