Evidence map›Paper›PMID 32518162›Full record

ArticleThe Journal of biological chemistry2020

Deciphering site 3 interactions of interleukin 12 and interleukin 23 with their cognate murine and human receptors.

Alessandra Esch, Anna Masiarz, Sofie Mossner, Jens M Moll, Joachim Grötzinger, Jutta Schröder, Jürgen Scheller, Doreen M Floss

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

13 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Alessandra EschInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Anna MasiarzInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Sofie MossnerInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Jens M MollInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Joachim GrötzingerInstitute of Biochemistry, Medical Faculty, Christian Albrechts University, Kiel, Germany.
Jutta SchröderInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Jürgen SchellerInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.ORCID 0000-0001-9932-1055
Doreen M FlossInstitute of Biochemistry and Molecular Biology II, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany doreen.floss@uni-duesseldorf.de.
Heinrich Heine University Düsseldorf · DEChristian-Albrechts-Universität zu Kiel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin (IL)-12 and IL-23 belong to the IL-12 type family and are composite cytokines, consisting of the common β subunit p40 and the specific cytokine α subunit p35 and p19, respectively. IL-12 signals via the IL-12Rβ1·IL-12Rβ2 receptor complex, and IL-23 uses also IL-12Rβ1 but engages IL-23R as second receptor. Importantly, binding of IL-12 and IL-23 to IL-12Rβ1 is mediated by p40, and binding to IL-12Rβ2 and IL-23R is mediated by p35 and p19, respectively. Previously, we have identified a W157A substitution at site 3 of murine IL-23p19 that abrogates binding to murine IL-23R. Here, we demonstrate that the analogous Y185R site 3 substitution in murine and Y189R site 3 substitution in human IL-12p35 abolishes binding to IL-12Rβ2 in a cross-species manner. Although Trp

Indexed as

Interleukin-12 Subunit p40Interleukin-23 Subunit p19Receptors, InterleukinReceptors, Interleukin-12Amino Acid SubstitutionAnimalsChlorocebus aethiopsCHO CellsCOS CellsCricetulusHEK293 CellsHumansMiceMutation, MissenseProtein BindingIL12B protein, humanIl12b protein, mouseIL12RB1 protein, humanIl12rb1 protein, mouseIL12RB2 protein, humanIl12rb2 protein, mouseIL23R protein, humanInterleukin-12 Subunit p40interleukin-23 receptor, mouseInterleukin-23 Subunit p19Receptors, InterleukinReceptors, Interleukin-12ERKIL-12IL-12Rbeta1IL-12Rbeta2IL-23IL-23Rinnate immunityinterleukinmitogen-activated protein kinase (MAPK)protein–protein interactionreceptrsignal transductionSTATSTAT3

Identifiers

PMID32518162
PMCPMC7383385
OpenAlexW3033060654

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.