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Enhancement of anti-HIV-1 activity by hot spot evolution of RANTES-derived peptides.
- Source :
-
Chemistry & biology [Chem Biol] 2012 Dec 21; Vol. 19 (12), pp. 1579-88. - Publication Year :
- 2012
-
Abstract
- CCR5, the major HIV-1 coreceptor, is a primary target for HIV-1 entry inhibition strategies. CCL5/RANTES, a natural CCR5 ligand, is one of the most potent HIV-1 entry inhibitors and, therefore, an ideal candidate to derive HIV-1 blockers. Peptides spanning the RANTES N-loop/β1-strand region act as specific CCR5 antagonists, with their hydrophobic N- and C termini playing a crucial role in virus blockade. Here, hydrophobic surfaces were enhanced by tryptophan substitution of aromatic residues, highlighting position 27 as a critical hot spot for HIV-1 blockade. In a further molecular evolution step, C-terminal engraftment of RANTES 40' loop produced a peptide with the highest solubility and anti-HIV-1 activity. These modified peptides represent leads for the development of effective HIV-1 inhibitors and microbicides.<br /> (Copyright © 2012 Elsevier Ltd. All rights reserved.)
- Subjects :
- Amino Acid Sequence
Amino Acid Substitution
Anti-HIV Agents metabolism
Anti-HIV Agents therapeutic use
CCR5 Receptor Antagonists
CD4-Positive T-Lymphocytes virology
Cells, Cultured
Chemokine CCL5 genetics
Chemokine CCL5 therapeutic use
HIV Infections drug therapy
HIV Infections prevention & control
Humans
Hydrophobic and Hydrophilic Interactions
Macrophages virology
Models, Molecular
Molecular Sequence Data
Peptides genetics
Peptides therapeutic use
Protein Conformation
Recombinant Proteins chemistry
Recombinant Proteins genetics
Recombinant Proteins pharmacology
Virus Internalization drug effects
Anti-HIV Agents chemistry
Anti-HIV Agents pharmacology
Chemokine CCL5 chemistry
Chemokine CCL5 pharmacology
HIV-1 drug effects
Peptides chemistry
Peptides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-1301
- Volume :
- 19
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Chemistry & biology
- Publication Type :
- Academic Journal
- Accession number :
- 23261601
- Full Text :
- https://doi.org/10.1016/j.chembiol.2012.10.007