IF 3.5 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Meg Critcher, Jia Meng Pang, Mia L Huang
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引用次数: 0

摘要

成纤维细胞生长因子 2(FGF2)是一种多能生长因子和信号蛋白,在多种细胞类型中具有广泛的功能。这些功能通常通过与生长因子受体结合而启动,并由称为蛋白聚糖的糖胺聚糖(GAG)修饰蛋白进行微调。FGF2 信号传导和功能的各种输出源于一组动态的、细胞类型特异的结合伙伴。然而,FGF2 的相互作用组尚未得到全面确定。此外,携带 GAG 链的蛋白多糖蛋白的身份往往被忽视,在大多数细胞环境中仍然未知。在这里,我们使用一种工程化的 APEX2-FGF2 融合蛋白进行过氧化物酶催化的活细胞近距离标记,以绘制 FGF2 的相互作用组图。在两个具有已确立的、不同的 FGF2 驱动功能的细胞系中,我们大大扩展了已知的 FGF2 相互作用组,发现了 >600 个新的推定 FGF2 相互作用体。值得注意的是,我们的研究结果证明了 FGF2 的 GAG 结合能力在调节其相互作用组中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping the FGF2 Interactome Identifies a Functional Proteoglycan Coreceptor.

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.

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来源期刊
ACS Chemical Biology
ACS Chemical Biology 生物-生化与分子生物学
CiteScore
7.50
自引率
5.00%
发文量
353
审稿时长
3.3 months
期刊介绍: ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology. The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies. We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.
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