Literature DB >> 2448952

Location of a major antigenic site involved in Ross River virus neutralization.

S Vrati1, C A Fernon, L Dalgarno, R C Weir.   

Abstract

The location of a major antigenic domain involved in the neutralization of an alphavirus, Ross River virus, has been defined in terms of its position in the amino acid sequence of the E2 glycoprotein. The domain encompasses three topographically close epitopes which were identified using three E2-specific neutralizing monoclonal antibodies in competitive binding assays. Nucleotide sequencing of the structural protein genes of monoclonal antibody-selected antigenic variants showed that for each variant there was a single nucleotide change in the E2 gene leading to a nonconservative amino acid substitution in E2. Changes were at positions 216, 234, and 246-251 in the amino acid sequence. The epitopes are in a region of E2 which, though not strongly conserved as to sequence among Ross River virus, Semliki Forest virus, and Sindbis virus, is conserved in its hydropathy profile among the three alphaviruses. The epitopes lie between two asparagine-linked glycosylation sites (residues 200 and 262) in E2. They are conserved as to position between the mouse virulent T48 strain and the mouse avirulent NB5092 strain.

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Year:  1988        PMID: 2448952     DOI: 10.1016/0042-6822(88)90474-6

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  33 in total

1.  An amino acid substitution in the coding region of the E2 glycoprotein adapts Ross River virus to utilize heparan sulfate as an attachment moiety.

Authors:  M L Heil; A Albee; J H Strauss; R J Kuhn
Journal:  J Virol       Date:  2001-07       Impact factor: 5.103

2.  Use of a lambda gt11 expression library to localize a neutralizing antibody-binding site in glycoprotein E2 of Sindbis virus.

Authors:  K S Wang; J H Strauss
Journal:  J Virol       Date:  1991-12       Impact factor: 5.103

3.  Identification of antigenically important domains in the glycoproteins of Sindbis virus by analysis of antibody escape variants.

Authors:  E G Strauss; D S Stec; A L Schmaljohn; J H Strauss
Journal:  J Virol       Date:  1991-09       Impact factor: 5.103

4.  The structure of barmah forest virus as revealed by cryo-electron microscopy at a 6-angstrom resolution has detailed transmembrane protein architecture and interactions.

Authors:  Victor A Kostyuchenko; Joanita Jakana; Xiangan Liu; Andrew D Haddow; Myint Aung; Scott C Weaver; Wah Chiu; Shee-Mei Lok
Journal:  J Virol       Date:  2011-07-13       Impact factor: 5.103

5.  Host alternation of chikungunya virus increases fitness while restricting population diversity and adaptability to novel selective pressures.

Authors:  Lark L Coffey; Marco Vignuzzi
Journal:  J Virol       Date:  2010-11-03       Impact factor: 5.103

Review 6.  Structural studies on antibody recognition and neutralization of viruses.

Authors:  Thomas James Smith
Journal:  Curr Opin Virol       Date:  2011-08       Impact factor: 7.090

7.  Suppressors of cleavage-site mutations in the p62 envelope protein of Semliki Forest virus reveal dynamics in spike structure and function.

Authors:  I Tubulekas; P Liljeström
Journal:  J Virol       Date:  1998-04       Impact factor: 5.103

8.  Structural localization of the E3 glycoprotein in attenuated Sindbis virus mutants.

Authors:  A M Paredes; H Heidner; P Thuman-Commike; B V Prasad; R E Johnston; W Chiu
Journal:  J Virol       Date:  1998-02       Impact factor: 5.103

Review 9.  The alphaviruses: gene expression, replication, and evolution.

Authors:  J H Strauss; E G Strauss
Journal:  Microbiol Rev       Date:  1994-09

10.  Genetic determinants of Sindbis virus mosquito infection are associated with a highly conserved alphavirus and flavivirus envelope sequence.

Authors:  Dennis J Pierro; Erik L Powers; Ken E Olson
Journal:  J Virol       Date:  2007-12-26       Impact factor: 5.103

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