Evidence map›Paper›PMID 39704408›Full record

ArticleACS chemical biology2025

Mapping the FGF2 Interactome Identifies a Functional Proteoglycan Coreceptor.

Meg Critcher, Jia Meng Pang, Mia L Huang

Abstract read
In one paragraph

Article in ACS chemical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

3 authors.

Meg CritcherDepartment of Chemistry, Scripps Research, 10550 N Torrey Pines Rd, La Jolla, California 92037, United States.
Jia Meng PangDepartment of Chemistry, Scripps Research, 10550 N Torrey Pines Rd, La Jolla, California 92037, United States.ORCID 0000-0002-7760-617X
Mia L HuangDepartment of Chemistry, Scripps Research, 10550 N Torrey Pines Rd, La Jolla, California 92037, United States.ORCID 0000-0001-9909-9554

Funding

Bridging the Glycome and Proteome with Chemical BiologyR35GM142462 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI Mia L Huang · 2021 to 2026
$2.9M
NIGMS NIH HHS R35 GM142462
6 · The paper itself

Abstract

Fibroblast growth factor 2 (FGF2) is a multipotent growth factor and signaling protein that exhibits broad functions across multiple cell types. These functions are often initiated by binding to growth factor receptors and fine-tuned by glycosaminoglycan (GAG)-modified proteins called proteoglycans. The various outputs of FGF2 signaling and functions arise from a dynamic and cell type-specific set of binding partners. However, the interactome of FGF2 has yet to be comprehensively determined. Moreover, the identity of the proteoglycan proteins carrying GAG chains is often overlooked and remains unknown in most cell contexts. Here, we perform peroxidase-catalyzed live cell proximity labeling using an engineered APEX2-FGF2 fusion protein to map the interactome of FGF2. Across two cell lines with established and distinct FGF2-driven functions, we greatly expand upon the known FGF2 interactome, identifying >600 new putative FGF2 interactors. Notably, our results demonstrate a key role for the GAG binding capacity of FGF2 in modulating its interactome.

Indexed as

Fibroblast Growth Factor 2ProteoglycansCell LineDNA-(Apurinic or Apyrimidinic Site) LyaseEndonucleasesGlycosaminoglycansHumansMultifunctional EnzymesProtein BindingSignal TransductionAPEX2 protein, humanDNA-(Apurinic or Apyrimidinic Site) LyaseEndonucleasesFibroblast Growth Factor 2GlycosaminoglycansMultifunctional EnzymesProteoglycans

Identifiers

PMID39704408
PMCPMC11858877

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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.