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A low-molecular-weight inhibitor against the chemokine receptor CXCR4: a strong anti-HIV peptide T140.

Authors :
Tamamura H
Xu Y
Hattori T
Zhang X
Arakaki R
Kanbara K
Omagari A
Otaka A
Ibuka T
Yamamoto N
Nakashima H
Fujii N
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.

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