Abstract
Background: The recently discovered small-molecule BI-2 potently blocks HIV-1 infection. BI-2 binds to the N-terminal domain of HIV-1 capsid. BI-2 utilizes the same capsid pocket used by the small molecule PF74. Although both drugs bind to the same pocket, it has been proposed that BI-2 uses a different mechanism to block HIV-1 infection when compared to PF74. Findings: This work demonstrates that BI-2 destabilizes the HIV-1 core during infection, and prevents the binding of the cellular factor CPSF6 to the HIV-1 core. Conclusions: Overall this short-form paper suggests that BI-2 is using a similar mechanism to the one used by PF74 to block HIV-1 infection.
| Original language | English (US) |
|---|---|
| Article number | 120 |
| Journal | Retrovirology |
| Volume | 11 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 11 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- BI-2
- CPSF6
- Capsid
- HIV-1
- PF74
- Stability
- Uncoating
ASJC Scopus subject areas
- Virology
- Infectious Diseases
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