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PMID: 15190071 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Solution structure and antibody binding studies of the envelope protein domain III from the New York strain of West Nile virus.

The Journal of biological chemistry ·Vol. 279 ·No. 37 ·2004-09-10 ·Pages 38755-61

Volk DE, Beasley DW, Kallick DA, Holbrook MR, Barrett AD, Gorenstein DG

Abstract

The solution structure of domain III from the New York West Nile virus strain 385-99 (WN-rED3) has been determined by NMR methods. The West Nile domain III structure is a beta-barrel structure formed from seven anti-parallel beta-strands in two beta-sheets. One anti-parallel beta-sheet consists of beta-strands beta1 (Phe(299)-Asp(307)), beta2 (Val(313)-Tyr(319)), beta4 (Arg(354)-Leu(355)), and beta5 (Lys(370)-Glu(376)) arranged so that beta2 is flanked on either side by beta1 and beta5. The short beta4 flanks the end of the remaining side of beta5. The remaining anti-parallel beta-sheet is formed from strands beta3 (Ile(340)-Val(343)), beta6 (Gly(380)-Arg(388)), and beta7 (Gln(391)-Lys(399)) arranged with beta6 at the center. Residues implicated in antigenic differences between different West Nile virus strains (and other flaviviruses) and neutralization are located on the outer surface of the protein. Characterization of the binding of monoclonal antibodies to WN-rED3 mutants, which were identified through neutralization escape experiments, indicate that antibody neutralization directly correlates with binding affinities. These studies provide an insight into theoretical virus-receptor interaction points, structure of immunogenic determinants, and potential targets for antiviral agents against West Nile virus and highlight differences between West Nile virus and other flavivirus structures that may represent critical determinants of virulence.

MeSH Terms
Antibodies, Monoclonal/chemistry Magnetic Resonance Spectroscopy Models, Molecular Mutation Protein Binding Protein Conformation Protein Structure, Secondary Protein Structure, Tertiary Viral Envelope Proteins/chemistry West Nile virus/metabolism,pathogenicity
Chemicals
Antibodies, Monoclonal Viral Envelope Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Volk David E
Sealy Center for Structural Biology, University of Texas Medical Branch, Galveston, Texas 77555-1147, USA.
Beasley David W C
Kallick Deborah A
Holbrook Michael R
Barrett Alan D T
Gorenstein David G
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2004-09-10
Epub
2004-00-09
Pages
38755-61
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIAID NIH HHS · T32 AI007536-06 · United States
PHS HHS · U01 A1054827 · United States
ODCDC CDC HHS · U90CCU618754 · United States
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PDB
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