Short Constrained Peptides That Inhibit HIV-1 Entry

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 99; no. 23; pp. 14664 - 14669
• Main Authors: Sia, Samuel K., Carr, Peter A., Cochran, Andrea G., Malashkevich, Vladimir N., Kim, Peter S.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 12.11.2002; National Acad Sciences
• Subjects: Amino Acid Sequence; Amino acids; Anti-HIV Agents - chemical synthesis; Anti-HIV Agents - chemistry; Anti-HIV Agents - pharmacology; Biochemistry; Biological Sciences; Calorimetry - methods; Circular Dichroism; Crystal structure; Crystallography, X-Ray; Enthalpy; Entropy; HIV; HIV 1; HIV Long Terminal Repeat - genetics; HIV-1 - drug effects; HIV-1 - physiology; Human immunodeficiency virus; Humans; Hydrogen Bonding; Inhibitory concentration 50; Oligopeptides - chemical synthesis; Oligopeptides - chemistry; Oligopeptides - pharmacology; Peptides; Radiocarbon; Spectroscopy; Thermodynamics; Titration
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.232566599

Peptides corresponding to the C-terminal heptad repeat of HIV-1 gp41 (C-peptides) are potent inhibitors of HIV-1 entry into cells. Their mechanism of inhibition involves binding in a helical conformation to the central coiled coil of HIV-1 gp41 in a dominant-negative manner. Short C-peptides, however, have low binding affinity for gp41 and poor inhibitory activity, which creates an obstacle to the development of small drug-like C-peptides. To improve the inhibitory potency of short C-peptides that target the hydrophobic pocket region of gp41, we use two strategies to stabilize the C-peptide helix: chemical crosslinking and substitution with unnatural helix-favoring amino acids. In this study, the short linear peptide shows no significant inhibitory activity, but a constrained peptide (C14linkmid) inhibits cell-cell fusion at micromolar potency. Structural studies confirm that the constrained peptides bind to the gp41 hydrophobic pocket. Calorimetry reveals that, of the peptides analyzed, the most potent are those that best balance the changes in binding enthalpy and entropy, and surprisingly not those with the highest helical propensity as measured by circular dichroism spectroscopy. Our study reveals the thermodynamic basis of inhibition of an HIV C-peptide, demonstrates the utility of constraining methods for a short antiviral peptide inhibitor, and has implications for the future design of constrained peptides.