Abstract
Full-length soluble HIV-1 Tat protein has been shown to bind the CXCR4 receptor. Occupancy of CXCR4 by Tat inhibits infection of cells by T-tropic HIV-1. To understand if fragments of the Tat protein may have similar anti-HIV activity, we synthesized Tat peptides and tested their activity in tissue culture. Here, we report a sequence-specific contribution of Tat residues 31-35 to anti-HIV-1 activity.
Original language | English (US) |
---|---|
Pages (from-to) | 609-613 |
Number of pages | 5 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 300 |
Issue number | 2 |
DOIs | |
State | Published - Jan 10 2003 |
Externally published | Yes |
Keywords
- Chemokine receptor
- Cyclic peptide
- Human immunodeficiency virus
- Tat protein
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology