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J Med Chem. 2004 Jul 15;47(15):3723-9.

A common pharmacophoric footprint for AIDS vaccine design.

Author information

1
Computational Molecular Biophysics, Interdisciplinary Center for Computational Science (IWR), University of Heidelberg, Im Neuenheimer Feld 368, 69120 Heidelberg, Germany.

Abstract

The most promising target antigen for an HIV vaccine designed using the classic antibody strategy has been the viral coat protein gp120. Unfortunately, its high variability has prevented this approach. We examine here a 15-residue peptide derived from the CD4-binding domain of gp120. By use of molecular dynamics computer simulation, it is shown that despite considerable sequence variation, the three-dimensional structure of the peptide is preserved over the full range of clade-specific sequences. Furthermore, sequences threaded onto the structure exhibit common three-dimensional electrostatic and hydrophobic properties. These common physicochemical characteristics constitute a pharmacophoric footprint that promises to be useful in the design of a synthetic antigen for vaccine development.

PMID:
15239651
DOI:
10.1021/jm031125s
[Indexed for MEDLINE]

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