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High-Throughput Screening Method of Inhibitors that Block the Interaction between 2 Helical Regions of HIV-1 gp41
- Source :
- SLAS Discovery. 10:13-19
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- The HIV-1 envelope glycoprotein transmembrane subunit, gp41, mediates the fusion of viral and target cell membranes. The 2 helical regions in the ectodomain of gp41, the N-helix and the C-helix, form a helical bundle complex that has been suggested as a fusion-active conformation. Previously, an enzyme-linked immunosorbent assay (ELISA) method had been established to measure the interaction of 2 helical regions of gp41. In this study, the ELISA method was modified to apply high-throughput screening (HTS) of an organic compound library. A few compounds had been identified to prevent the interaction between 2 helical regions of gp41, and they were further shown to inhibit the gp41-mediated viral infection. In addition, they specifically quenched the fluorescence of tryptophan in the N-helix region, indicating that these compounds bound to the N-helix rather than the C-helix of gp41. These results suggested that this assay method targeting gp41 could be used for HTS of HIV fusion inhibitors. (Journal of Biom...
- Subjects :
- 0301 basic medicine
Anti-HIV Agents
viruses
Protein subunit
High-throughput screening
Drug Evaluation, Preclinical
Biology
Gp41
01 natural sciences
Biochemistry
Protein Structure, Secondary
Cell Line
Analytical Chemistry
03 medical and health sciences
Humans
chemistry.chemical_classification
Molecular Structure
Tryptophan
Reproducibility of Results
virus diseases
Lipid bilayer fusion
HIV Envelope Protein gp41
Transmembrane protein
0104 chemical sciences
010404 medicinal & biomolecular chemistry
Spectrometry, Fluorescence
030104 developmental biology
Membrane
Ectodomain
chemistry
HIV-1
Molecular Medicine
Glycoprotein
Protein Binding
Biotechnology
Subjects
Details
- ISSN :
- 24725552
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- SLAS Discovery
- Accession number :
- edsair.doi.dedup.....a4db10e9a1c5285801a51738ac0198d3
- Full Text :
- https://doi.org/10.1177/1087057104269726