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Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides

Dissertation (MSc (Genetics))--University of Pretoria, 2010.

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Other Authors: Huismans, H. (Henk), 1942-
Format: Thesis
Published: University of Pretoria 2013
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access_status_str Open Access
author2 Huismans, H. (Henk), 1942-
author_browse Huismans, H. (Henk), 1942-
author_facet Huismans, H. (Henk), 1942-
collection Thesis
dc_rights_str_mv © 2006 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Genetics))--University of Pretoria, 2010.
format Thesis
id oai:repository.up.ac.za:2263/26150
institution University of Pretoria (South Africa)
last_indexed 2026-06-10T12:38:33.924Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2013
publishDateRange 2013
publishDateSort 2013
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/26150 Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides Huismans, H. (Henk), 1942- klacheiner@yahoo.com Lacheiner, Karen African horse sickness (AHS) Ns1 Hydrophobic protein UCTD Dissertation (MSc (Genetics))--University of Pretoria, 2010. Non-structural protein, NS1 of African horse sickness virus is a hydrophobic protein of 63 kDa that spontaneously assembles into highly distinct tubular structures when expressed in mammalian or insect cells. The spontaneous assembly of these proteins into a predictable multimeric structure, high levels of expression and ease of purification make this protein an ideal candidate for the immune display of foreign peptides. The potential of such a display system has been investigated for BTV NS1 that is able to successfully elicit both a humoral and a cellular immune response against inserted peptides. The aims of this study were to investigate both the stability of the AHSV NS1 particulate structure after insertion of peptides as well as the antigenicity and immunogenicity of the peptides presented in this system. Two overlapping regions consisting of 40 and 150 amino acids, and which correspond to a neutralising region identified within the AHSV major neutralising protein VP2, were inserted into an internal site in NS1. This site offered the best surface display of inserted peptides on the tubular structures. An enhanced green fluorescent protein, 240 amino acids long, was also inserted into the NS1 protein. Sucrose gradient analysis of the recombinant proteins indicated that the majority of the baculovirus expressed chimeric proteins formed particulate structures with a sedimentation value similar to that of the native NS1 protein. This was confirmed by transmission electron microscopic analysis, which clearly showed that all the chimeric proteins assembled into tubular structures similar to those observed for AHSV NS1 proteins. Furthermore, fluorescence analysis of sucrose gradients of NS1/eGFP also showed high levels of fluorescence that corresponded directly to particle formation. Not only do the inserts remain functional but are also presented successfully on the surface of the intact NS1 tubule structure. The potential of the NS1 vector to efficiently present peptides to the immune system was subsequently investigated. The serums generated against these chimeric proteins in guinea pigs were tested against chimeric constructs, the baculovirus expressed inserts (for eGFP) and the inserts presented on other presentation vectors. Western blot analysis showed that most of the serums generated against the chimeric proteins contained antibodies not only against the chimeric proteins but antibodies that reacted specifically with the inserted peptides on their own or on another presentation system. Preliminary immune studies seem to indicate that the humoral immune response elicited by the chimeric NS1 proteins is predominantly against the inserts. The inserts are successfully presented to the immune system on the surface of the NS1 vector and are able to elicit the production of antibodies with the potential to provide a protective immune response. Genetics unrestricted 2013-09-07T02:52:36Z 2008-07-16 2013-09-07T02:52:36Z 2007-04-20 2010-07-16 2008-07-09 Dissertation Lacheiner, K 2006, Tubules composed of non-structural protein NS1 of African horsesickness virus as a system for the immune display of foreign peptides, MSc dissertation, University of Pretoria, Pretoria, viewed yymmdd < http://hdl.handle.net/2263/26150 > E545/ag http://hdl.handle.net/2263/26150 http://upetd.up.ac.za/thesis/available/etd-07092008-103908/ © 2006 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle African horse sickness (AHS)
Ns1
Hydrophobic protein
UCTD
Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides
title Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides
title_full Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides
title_fullStr Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides
title_full_unstemmed Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides
title_short Tubules composed of non-structural protein NS1 of african horsesickness virus as system for the immune display of foreign peptides
title_sort tubules composed of non structural protein ns1 of african horsesickness virus as system for the immune display of foreign peptides
topic African horse sickness (AHS)
Ns1
Hydrophobic protein
UCTD
url http://hdl.handle.net/2263/26150
http://upetd.up.ac.za/thesis/available/etd-07092008-103908/