1meq

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Revision as of 12:13, 8 November 2007

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HIV gp120 C5

Overview

In HIV the viral envelope protein is processed by a host cell protease to, form gp120 and gp41. The C1 and C5 domains of gp120 are thought to, directly interact with gp41 but are largely missing from the available, X-ray structure. Biophysical studies of the HIV gp120 C5 domain (residues, 489-511 of HIV-1 strain HXB2), which corresponds to the carboxy terminal, region of gp120, have been undertaken. CD studies of the C5 domain suggest, that it is unstructured in aqueous solutions but partially helical in, trifluoroethanol/aqueous and hexafluoroisopropanol/aqueous buffers. The, solution structure of the C5 peptide in 40% trifluoroethanol/aqueous, buffer was determined by NMR spectroscopy. The resulting structure is a, turn helix structural motif, consistent with the CD results. Fluorescence, titration experiments suggest that HIV C5 forms a 1 : 1 complex with the, HIV gp41 ectodomain in the presence of cosolvent with an apparent Kd of, approximately 1.0 micro m. The absence of complex formation in the absence, of cosolvent indicates that formation of the turn-helix structural motif, of C5 is necessary for complex formation. Examination of the C5 structure, provides insight into the interaction between gp120 and gp41 and provides, a possible target site for future drug therapies designed to disrupt the, gp120/gp41 complex. In addition, the C5 structure lends insight into the, site of HIV envelope protein maturation by the host enzymes furin and PC7, which provides other possible targets for drug therapies.

About this Structure

1MEQ is a Single protein structure of sequence from [1]. Full crystallographic information is available from OCA.

Reference

Solution structure of the HIV gp120 C5 domain., Guilhaudis L, Jacobs A, Caffrey M, Eur J Biochem. 2002 Oct;269(19):4860-7. PMID:12354117

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