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Peptide-poly(L-lysine citramide) conjugates and their in vitro anti-HIV behavior.
- Source :
-
Biomacromolecules [Biomacromolecules] 2009 Apr 13; Vol. 10 (4), pp. 865-76. - Publication Year :
- 2009
-
Abstract
- Poly(L-lysine citramide) is a degradable bioresorbable polyanion whose polyamide chains are composed of citric acid and L-lysine building blocks. Its chemical and physicochemical properties were extensively investigated in the past for its interest as polymeric drug carrier. In this work, 4(S)-amino-3-(S)-hydroxy-5-phenylpentanoyl-isoleucyl-phenylalanine methyl ester, a pseudopeptide active against the HIV protease in vitro, was linked to poly(L-lysine citramide) in attempts to promote solubility and cell penetration. Conjugates were characterized by FTIR, NMR, SEC, DLS, amino-acid analyses, and toxicity in mice. They degraded slowly at pH 7.4 and more rapidly at pH 4.5, two pH values selected to mimic extra-cellular fluids and intralysosome medium, respectively. According to capillary zone electrophoresis, degradation did not release the peptide. The phenylalanyl-isoleucyl-phenylalanine methyl ester peptide, inactive against the protease in vitro, was used as negative control. The anti-HIV activities of the carrier, of the conjugates and of model molecules, including a fluorescence-labeled pseudopeptide conjugate, were evaluated comparatively in vitro using two cell lines, namely, CEM-SS and MT-4 cells, infected with HIV-1 LAI and IIIB isolates, respectively. Unexpectedly, all the conjugates showed in vitro antiviral activity independent of peptide release and of inhibition of the HIV protease. According to FACS analysis, the antiviral activity was related to the presence of peptide moieties along the polymer chains and depended on the order by which cells, viruses, and conjugates were presented to each other. Although it was not possible to determine whether the antiviral activity resulted from interactions between conjugates and cells or conjugates and virus or both, the conjugates appeared able to inhibit the binding of the virus to cells in vitro when introduced before cell infection. None of the conjugates exhibited acute toxicity in mice.
- Subjects :
- Animals
Anti-HIV Agents chemistry
Body Weight drug effects
Cell Line
Chromatography, Thin Layer
Enzyme-Linked Immunosorbent Assay
Female
Flow Cytometry
HIV Protease Inhibitors chemistry
HIV Protease Inhibitors pharmacology
HIV-1 metabolism
Humans
Inhibitory Concentration 50
Lymphocytes cytology
Lymphocytes metabolism
Lysine chemistry
Magnetic Resonance Spectroscopy
Mice
Peptide Fragments chemistry
Polylysine chemistry
Polylysine pharmacology
Polymers
Spectroscopy, Fourier Transform Infrared
Anti-HIV Agents pharmacology
HIV Infections drug therapy
HIV-1 drug effects
Lymphocytes drug effects
Peptide Fragments pharmacology
Polylysine analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1526-4602
- Volume :
- 10
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Biomacromolecules
- Publication Type :
- Academic Journal
- Accession number :
- 19296658
- Full Text :
- https://doi.org/10.1021/bm801376v