The design of a specific ligand of HIV gp120

J Pept Sci. 1997 Sep-Oct;3(5):383-90. doi: 10.1002/(SICI)1099-1387(199709)3:5%3C383::AID-PSC123%3E3.0.CO;2-C.

Abstract

The crystal structure of CD4 suggested that the C/G38 and C/L44 replacements with the consequent cystine bridge formation are compatible with the native structure of that molecular moiety. As the NQGSF sequence, corresponding to the 39-43 fragment of human CD4 protein, was found to be involved in the HIV gp120 interaction, it has been synthesized in a cyclic form by adding two cysteine residues at the amino and carboxy termini. 1H-NMR studies show that the predominant solution conformation of cyclo-[CNQGSFC] is a type II beta-turn centred on the NQGS segment. Structural and dynamic properties of the peptide are also analysed in relation to the in vitro activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • CD4 Antigens / chemistry*
  • CD4 Antigens / metabolism
  • Giant Cells / drug effects
  • Giant Cells / virology
  • HIV Envelope Protein gp120 / metabolism*
  • Humans
  • Ligands
  • Magnetic Resonance Spectroscopy
  • Oligopeptides / chemistry*
  • Oligopeptides / pharmacology
  • Peptides, Cyclic / chemistry*
  • Peptides, Cyclic / pharmacology
  • Protein Conformation

Substances

  • CD4 Antigens
  • HIV Envelope Protein gp120
  • Ligands
  • Oligopeptides
  • Peptides, Cyclic