Abstract
The viral peptide fusion inhibitor Fuzeon (T-20/DP178/enfuvirtide) is an essential part of the drug combination that has significantly increased the quality of life and life span of many acquired immuno-deficiency syndrome (AIDS) patients. Its development as a drug preceded the elucidation of its precise inhibitory mechanism, as well as its molecular targets. The initial model was that Fuzeon inhibits human immunodeficiency virus (HIV) entry by targeting one site within the viral transmembrane envelope protein. Herein, we describe the emerging discoveries that extend this model towards a multifaceted mechanism for the drug in targeting HIV. This significantly advances the understanding of how viruses enter host cells and opens a new window of opportunity for designing future viral fusion inhibitors.
| Original language | English |
|---|---|
| Pages (from-to) | 2352-2358 |
| Number of pages | 7 |
| Journal | Biochimica et Biophysica Acta - Biomembranes |
| Volume | 1808 |
| Issue number | 10 |
| DOIs | |
| State | Published - 1 Oct 2011 |
| Externally published | Yes |
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
- HIV entry inhibitor
- Membrane fusion
- Transmembrane protein
- Viral envelope protein
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Cell Biology
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