Evidence map›Paper›PMID 40994246›Full record

ArticleFEBS open bio2026

Cloning, expression, purification, and structural modeling of the Chandipura virus matrix protein.

Mariana Grieben

Abstract read
In one paragraph

Article in FEBS open bio, 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

1 author.

Mariana GriebenInstitute of Biochemistry, Center of Structural and Cell Biology in Medicine, University of Lübeck, Germany.ORCID https://orcid.org/0000-0002-0685-6868

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Chandipura virus matrix protein plays a crucial role in virus assembly, budding, and the cytopathic effects observed in infected cells by interacting with several host proteins. The protocol presented here outlines the expression and purification of full-length Chandipura virus matrix protein and two N-terminally truncated constructs produced in Escherichia coli. This protocol results in high yields of monomeric matrix protein, which is suitable for structural studies. Additionally, GFP-fused Chandipura virus matrix protein constructs can be expressed in mammalian cells for examination of intracellular localization. The Chandipura virus matrix protein model, generated using AlphaFold, features an intrinsically disordered N terminus and a structured C-terminal core, similar to other Vesiculovirus matrix proteins.

Indexed as

VesiculovirusViral Matrix ProteinsAnimalsCloning, MolecularEscherichia coliHumansModels, MolecularViral Matrix ProteinsChandipura virusChandipura virus matrix proteincloningencephalitisexpressionpurificationVesiculovirus

Identifiers

PMID40994246
PMCPMC12767760

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.