Evidence map›Paper›PMID 29035299›Full record

ArticleInternational journal of molecular sciences2017

Two Distinct Conformations in Bet v 2 Determine Its Proteolytic Resistance to Cathepsin S.

Wai Tuck Soh, Peter Briza, Elfriede Dall, Claudia Asam, Mario Schubert, Sara Huber, Lorenz Aglas, Barbara Bohle, Fatima Ferreira, Hans Brandstetter

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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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

10 authors.

Wai Tuck SohDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. waituck.soh@sbg.ac.at.ORCID 0000-0003-0082-7983
Peter BrizaDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. Peter.Briza@sbg.ac.at.
Elfriede DallDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. Elfriede.dall@sbg.ac.at.
Claudia AsamDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. claudia.asam@sbg.ac.at.
Mario SchubertDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. mario.schubert@sbg.ac.at.ORCID 0000-0003-0278-4091
Sara HuberDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. Sara.Huber@stud.sbg.ac.at.
Lorenz AglasDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. lorenz.aglas@sbg.ac.at.
Barbara BohleDepartment of Pathophysiology, Medical University of Vienna, Vienna 1090, Austria. barbara.bohle@meduniwien.ac.at.
Fatima FerreiraDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. Fatima.Ferreira@sbg.ac.at.ORCID 0000-0003-0989-2335
Hans BrandstetterDepartment of Molecular Biology, University of Salzburg, Salzburg 5020, Austria. hans.brandstetter@sbg.ac.at.ORCID 0000-0002-6089-3045

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Birch pollen allergy affects more than 20% of the European allergic population. On a molecular level, birch pollen allergy can be linked to the two dominant allergens Bet v 1 and Bet v 2. Bet v 2 belongs to the profilin family, which is abundant in the plant kingdom. Importantly, the homologous plant profilins have a conserved cysteine motif with a currently unknown functional relevance. In particular, it is unknown whether the motif is relevant for disulfide formation and to what extent it would affect the profilins' structural, functional and immunological properties. Here we present crystal structures of Bet v 2 in the reduced and the oxidized state, i.e., without and with a disulfide bridge. Despite overall structural similarity, the two structures distinctly differ at their termini which are stabilized to each other in the oxidized, i.e., disulfide-linked state. These structural differences translate into differences in their proteolytic resistance. Whereas the oxidized Bet v 2 is rather resistant towards the endolysosomal protease cathepsin S, it is rapidly degraded in the reduced form. By contrast, both Bet v 2 forms exhibit similar immunological properties as evidenced by their binding to IgE antibodies from birch pollen allergic patients and by their ability to trigger histamine release in a humanized rat basophilic leukemia cells (RBL) assay, independent of the presence or absence of the disulfide bridge. Taken together our findings suggest that the oxidized Bet v 2 conformation should be the relevant species, with a much longer retention time to trigger immune responses.

Indexed as

Models, MolecularProtein ConformationAntigens, PlantCathepsinsCloning, MolecularEndosomesLysosomesOxidation-ReductionProteolysisSolutionsStructure-Activity RelationshipAntigens, PlantBETV2 protein, Betula pendulacathepsin SCathepsinsSolutionsallergenendolysosomal proteasespanallergenpost-translational modification

Identifiers

PMID29035299
PMCPMC5666837

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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.