Detailed Information on Publication Record
2023
Unravelling Tick-Borne Encephalitis Virus Neutralisation Mechanisms with Cryo-EM
NEPOVÍMOVÁ, Lucie, Tibor FÜZIK, Lenka ŠMERDOVÁ and Pavel PLEVKABasic information
Original name
Unravelling Tick-Borne Encephalitis Virus Neutralisation Mechanisms with Cryo-EM
Name in Czech
Odhalení mechanismů neutralizace viru klíšťové encefalitidy pomocí Cryo-EM
Authors
NEPOVÍMOVÁ, Lucie (203 Czech Republic, belonging to the institution), Tibor FÜZIK (703 Slovakia, belonging to the institution), Lenka ŠMERDOVÁ (203 Czech Republic, belonging to the institution) and Pavel PLEVKA (203 Czech Republic, guarantor, belonging to the institution)
Edition
VBC Cryo-EM Symposium, 2023
Other information
Language
English
Type of outcome
Konferenční abstrakt
Field of Study
10607 Virology
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
RIV identification code
RIV/00216224:14740/23:00134306
Organization unit
Central European Institute of Technology
Keywords in English
TBEV; cryo-EM; antibodies
Tags
Tags
International impact, Reviewed
Změněno: 27/3/2024 11:10, Mgr. Eva Dubská
Abstract
V originále
Tick-borne encephalitis (TBE), caused by the tick-borne encephalitis virus (TBEV), is a severe disease that can lead to fatal central nervous system inflammation. Despite the availability of vaccines, vaccination rates in the most affected areas, such as the Czech Republic, are low. With TBE cases on the rise, the need for targeted treatments is growing. Antibodies have shown promise in a mouse model, where intravenous administration of TBEV-specific antibodies served as a treatment. However, our understanding of the molecular mechanisms behind TBEV neutralisation remains limited.To address this gap, we investigated the interactions between the TBEV Neudörfl strain and two neutralising mouse monoclonal antibodies, IC3 and A4, which bind to distinct domains of the TBEV envelope protein. We purified TBEV from infected tissue culture cells, mixed it with Fab fragments derived from the neutralising antibodies, and vitrified the samples on grids for cryo-electron microscopy. Using single-particle analysis, we solved the structures of the TBEV-Fab complexes from the collected micrographs.By deciphering the molecular basis of TBEV neutralisation by antibodies, we aim to gain insights into the significance of different epitopes on the viral surface. This knowledge may pave the way for the tailored design of therapeutic antibodies or more specific vaccines in the future.
Links
GX19-25982X, research and development project |
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