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Secreted trimeric viral envelope proteins as a tool for new vaccine design and biochemical assays
Vladimir Pekařík
Jazyk angličtina Země Česko
Typ dokumentu přehledy
NLK
Open Access Digital Library
od 2014-01-01
- MeSH
- genové produkty env - virus lidské imunodeficience MeSH
- genové produkty env MeSH
- hemaglutininové glykoproteiny viru chřipky MeSH
- imunogenetické jevy MeSH
- lektiny vázající mannosu MeSH
- multimerizace proteinu * MeSH
- neutralizující protilátky MeSH
- proteinové inženýrství MeSH
- proteiny - lokalizační signály MeSH
- proteiny virového obalu * MeSH
- rekombinantní fúzní proteiny chemie MeSH
- rostlinné lektiny MeSH
- Saccharomyces cerevisiae - proteiny MeSH
- transkripční faktory bZIP MeSH
- virové vakcíny * chemie MeSH
- Publikační typ
- přehledy MeSH
Varies viral envelope proteins are formed by trimeric modules that are highly stable while anchored through the transmembrane domain in the virus membrane. Unfortunately, to raise vaccines against the whole viruses could lead to the production of antibodies against hijacked cellular proteins that can cause adverse effects. Therefore, pure protein preparations are used for vaccines production. It was found that the use of monomeric immunogens is insufficient in induction of neutralising antibodies. Protective antibodies were more often produced when trimeric ENV proteins were used. Here, we describe technical aspects of ENV proteins processing in host cells, the way to construct stable trimeric immunogens, and recent progress with construction of soluble trimers of ENV from Ebola, HIV, rabies, and influenza viruses.
Central European Institute of Technology Masaryk University Brno Czech Republic European Union
Department of Physiology Faculty of Medicine Masaryk University Brno Czech Republic European Union
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- $a Secreted trimeric viral envelope proteins as a tool for new vaccine design and biochemical assays / $c Vladimir Pekařík
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- $a Varies viral envelope proteins are formed by trimeric modules that are highly stable while anchored through the transmembrane domain in the virus membrane. Unfortunately, to raise vaccines against the whole viruses could lead to the production of antibodies against hijacked cellular proteins that can cause adverse effects. Therefore, pure protein preparations are used for vaccines production. It was found that the use of monomeric immunogens is insufficient in induction of neutralising antibodies. Protective antibodies were more often produced when trimeric ENV proteins were used. Here, we describe technical aspects of ENV proteins processing in host cells, the way to construct stable trimeric immunogens, and recent progress with construction of soluble trimers of ENV from Ebola, HIV, rabies, and influenza viruses.
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