Document Detail


Effects of domain-switching and site-directed mutagenesis on the properties and functions of the VP7 proteins of two orbiviruses.
MedLine Citation:
PMID:  9356334     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Based on the crystal structure of the VP7 major core protein of bluetongue virus serotype 10 (BTV-10) and that of the top domain of the VP7 protein of African horsesickness virus serotype 4 (AHSV-4), chimeras and site-directed mutants of the proteins were constructed and the products analyzed with respect to their properties and functions. Chimeras with the central upper domain of BTV-10 VP7 replaced by that of AHSV-4 VP7 (construct BAB) formed trimers, as did the converse construct (ABA). Further, both proteins exhibited the expected conformational epitopes of the constituent sequences. Using BAB VP7 it was demonstrated that residues of the upper domain of AHSV-4 VP7 contribute to the observed insolubility of the protein. By contrast, ABA VP7 protein was as soluble as wild-type BTV-10 VP7. Replacement of selected amino acid residues in the top domain (e.g., A167 by R; F209 by T) improved the solubility of BAB VP7. Since the trimeric BAB and ABA VP7 proteins did not form core-like particles (CLPs) when coexpressed with BTV VP3, it was concluded that trimerization of chimeric VP7 is not sufficient for CLP formation. When the N-terminal region of the ABA protein (aa 1-120) was replaced by the respective sequences of BTV VP7 (construct BBA), the protein aggregated and did not form CLPs with coexpressed BTV VP3, most likely due to disruption of the required contacts between the N- and C-terminal regions of the bottom domain, leading to incorrect folding of the chimera.
Authors:
K Monastyrskaya; N Staeuber; G Sutton; P Roy
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Virology     Volume:  237     ISSN:  0042-6822     ISO Abbreviation:  Virology     Publication Date:  1997 Oct 
Date Detail:
Created Date:  1997-12-02     Completed Date:  1997-12-02     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0110674     Medline TA:  Virology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  217-27     Citation Subset:  IM    
Copyright Information:
Copyright 1997 Academic Press.
Affiliation:
Department of Biochemistry, University of Oxford, Oxford, OX1 3QU, United Kingdom.
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MeSH Terms
Descriptor/Qualifier:
Amino Acid Substitution
Antigens, Viral / genetics
Capsid / genetics*
Capsid Proteins*
Gene Expression Regulation, Viral*
Mutagenesis, Site-Directed
Orbivirus / genetics*,  metabolism
Recombinant Fusion Proteins / genetics
Transfection
Viral Core Proteins / genetics
Chemical
Reg. No./Substance:
0/Antigens, Viral; 0/Capsid Proteins; 0/Recombinant Fusion Proteins; 0/VP7 protein, Rotavirus; 0/Viral Core Proteins; 138413-77-1/VP7 major core antigen, African horsesickness virus

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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