Evidence map›Paper›PMID 42397903›Full record

ArticleScience advances2026

Structures of asymmetric particles of tick-borne encephalitis virus provide insight into flavivirus assembly and maturation.

Tibor Füzik, Maria Anastasina, Peter Pajtinka, Ausra Domanska, Lauri I A Pulkkinen, Lenka Šmerdová, Lucie Nepovímová, Petra Formanová-Pokorná, Petra Straková, Jiří Nováček and 4 more

Abstract read
In one paragraph

Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Tibor FüzikCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0002-1190-0210
Maria AnastasinaFaculty of Biological and Environmental Sciences, Department of Molecular and Integrative Biosciences, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-4555-6446
Peter PajtinkaCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0009-0007-8162-4227
Ausra DomanskaFaculty of Biological and Environmental Sciences, Department of Molecular and Integrative Biosciences, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-3772-6003
Lauri I A PulkkinenFaculty of Biological and Environmental Sciences, Department of Molecular and Integrative Biosciences, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-3919-2498
Lenka ŠmerdováCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0001-8043-0921
Lucie NepovímováCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0009-0009-6978-8063
Petra Formanová-PokornáLaboratory of Emerging Viral Infections, Veterinary Research Institute, Brno, Czech Republic.ORCID 0009-0002-6086-1665
Petra StrakováLaboratory of Emerging Viral Infections, Veterinary Research Institute, Brno, Czech Republic.ORCID 0000-0002-3130-933X
Jiří NováčekCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0003-4013-3898
Daniel RůžekLaboratory of Emerging Viral Infections, Veterinary Research Institute, Brno, Czech Republic.ORCID 0000-0003-4655-2380
Robert VáchaCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0001-7610-658X
Sarah J ButcherFaculty of Biological and Environmental Sciences, Department of Molecular and Integrative Biosciences, University of Helsinki, Helsinki, Finland.ORCID 0000-0001-7060-5871
Pavel PlevkaCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.ORCID 0000-0003-4215-3315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flaviviruses are globally distributed human pathogens. However, the mechanisms underlying flavivirus assembly and maturation remain poorly understood. Here, we show that many particles of tick-borne encephalitis virus (TBEV) are asymmetric and lack subsets of surface heterodimers. Immature particles of TBEV contain incomplete spikes, providing evidence that their coats assemble directly from heterodimers of premembrane (prM) and envelope (E) proteins. Exposure of TBEV particles to acidic pH in the Golgi complex promotes maturation. The spikes and herringbone regions in TBEV maturation intermediates are oriented randomly rather than conforming to a common icosahedral symmetry. Consequently, the mature herringbone lattice forms around a randomly oriented nucleation center, expanding by addition of membrane-envelope heterodimers as the spikes disassemble and prMs are cleaved. The observed incompleteness of the protein coats explains, as an alternative to particle breathing, how flaviviruses can be neutralized by antibodies that bind to regions of E proteins normally inaccessible in the spiky or herringbone structures.

Indexed as

Encephalitis Viruses, Tick-BorneVirionVirus AssemblyAnimalsHumansViral Envelope ProteinsViral Envelope Proteins

Identifiers

PMID42397903
PMCPMC13330823

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.