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A low-molecular-weight inhibitor against the chemokine receptor CXCR4: a strong anti-HIV peptide T140.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1998 Dec 30; Vol. 253 (3), pp. 877-82. - Publication Year :
- 1998
-
Abstract
- T22 ([Tyr5,12, Lys7]-polyphemusin II) is an 18-residue peptide amide, which has strong anti-HIV activity. T22 inhibits the T cell line-tropic (T-tropic) HIV-1 infection through its specific binding to a chemokine receptor CXCR4, which serves as a coreceptor for the entry of T-tropic HIV-1 strains. Herein, we report our finding of novel 14-residue CXCR4 inhibitors, T134 and T140, on the basis of the T22 structure. In the assays we examined, T140 showed the highest inhibitory activity against HIV-1 entry and the strongest inhibitory effect on the binding of an anti-CXCR4 monoclonal antibody (12G5) to CXCR4 among all the CXCR4 inhibitors that have been reported up to now.
- Subjects :
- Amino Acid Sequence
Anti-HIV Agents toxicity
Benzylamines
Cells, Cultured
Chemokine CXCL12
Chemokines, CXC pharmacology
Circular Dichroism
Cyclams
DNA-Binding Proteins chemistry
Heterocyclic Compounds pharmacology
Molecular Sequence Data
Oligopeptides chemistry
Oligopeptides toxicity
Peptides chemistry
Peptides pharmacology
Peptides, Cyclic chemistry
Anti-HIV Agents pharmacology
Antimicrobial Cationic Peptides
HIV-1 drug effects
Oligopeptides pharmacology
Receptors, CXCR4 antagonists & inhibitors
T-Lymphocytes virology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 253
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 9918823
- Full Text :
- https://doi.org/10.1006/bbrc.1998.9871