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Record W4403830851 · doi:10.1681/asn.2024d9wqkf8b

Identification of Crb2 Partner Proteins in Podocytes Using BioID

2024· article· en· W4403830851 on OpenAlexaff
Soichiro SUZUKI, Sajida Ibrahim, Lamine Aoudjit, Simon Leclerc, Serge Lemay, Tomoko Takano

Bibliographic record

VenueJournal of the American Society of Nephrology · 2024
Typearticle
Languageen
FieldMedicine
TopicMonoclonal and Polyclonal Antibodies Research
Canadian institutionsMcGill University Health Centre
Fundersnot available
KeywordsIdentification (biology)Computational biologyCell biologyPodocyteBiologyMedicineKidneyGeneticsProteinuria

Abstract

fetched live from OpenAlex

Background: Crb2 is an essential protein expressed at the slit diaphragm of podocytes and its mutations cause hereditary nephrotic syndrome. We also reported that anti-Crb2 antibodies may be causal in idiopathic nephrotic syndrome. However, how Crb2 functions in podocytes is not fully understood. To obtain insight into the signaling pathways of Crb2, we conducted proximity-dependent biotinylation and proteomics (BioID). Methods: BioID is based on the fusion of a promiscuous E.coli biotin ligase (BirA) to a target protein, Crb2. Intracellular domain of human Crb2 (1223-1285aa) was subcloned downstream of the extracellular/transmembrane domain of IL2R, conjugated with BirA, and expressed in human podocytes. As a control, human podocytes expressing GFP-BirA were used. Biotinylated proteins were captured and analyzed by mass spectrometry. Results (n=3) were analyzed using Scaffold 5. Results: Protein identification by BioID revealed 328 proteins exhibiting significant interaction with Crb2 (compared with GFP-control, p<0.05). Identified proteins were analyzed by enrichment analysis using Reactome pathways and gene ontology annotations. The results showed that Crb2 partner proteins are predominantly involved in Rho, Rac and Cdc42 GTPase signaling pathways, covering 20 out of the 25 most significantly enriched Reactome pathways. Furthermore, Crb2 interactors significantly contribute to actin cytoskeleton organization (GO ID 30036, adjusted p-Value 4.70E-08) and cell adhesion (GO ID 7155, adjusted p-Value 1.91E-06). Of interest, ARHGEF26, an upstream activator of Rho family proteins, was identified as one of the Crb2 interactors. We confirmed the interaction by co-immunoprecipitation and immunostaining showed ARHGEF26 and Crb2 colocalization in both immortalized human podocytes and mouse glomeruli. Analysis of public scRNAseq datasets showed that ARHGEF26 expression in the kidney is highly specific to podocytes. CRISPR/Cas9 KO of ARHGEF26 in podocytes reduced RhoA and Rac1 activation as well as cell projection formation in response to EGF. Conclusion: Crb2 plays a crucial role as a cytoskeletal regulatory protein in podocytes, and alterations in Crb2 signaling will likely lead to cytoskeletal changes and subsequent podocyte injury. We are investigating the identified proteins to elucidate their roles in Crb2 signaling, with the goal to identify novel therapeutic targets.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0020.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.041
GPT teacher head0.366
Teacher spread0.325 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2024
Admission routes1
Has abstractyes

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