素-2的相互作用学揭示了与GAPDH的相互作用以及在糖解中酸化介导的调节作用
Paula Turkki1,2, Iftekhar Chowdhury3, Tiina Öhman3
1Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Scientific reports
|August 27, 2024
概括
素-2是一种对细胞粘附至关重要的蛋白质,与糖分解酶GAPDH相互作用. 它在Y483的酸化调节了细胞能量代谢和粘附.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 集成因子适配蛋白,如素-2,在细胞粘附和信号传递中起着至关重要的作用.
- 除了在焦点粘附处的局部化之外,tensin-2的精确功能尚未完全理解.
研究的目的:
- 为了确定tensin-2的新型相互作用伙伴.
- 研究素-2在细胞代谢和信号传递中的作用.
主要方法:
- 靠近性依赖生物化和Strep-tag亲和蛋白质组学被用来识别张素-2相互作用体.
- 细胞糖解率是作为对素-2酸化的反应而测量的.
主要成果:
- 发现素-2与已知的焦点粘附蛋白,素糖蛋白复合体和糖溶性酶GAPDH相互作用.
- 素-2在氨酸483 (Y483) 的酸化被证明可以调节细胞的糖分分解率.
- 酸化张素-2 (pY483) 被观察到在焦点粘附中得到丰富.
结论:
- 这项研究确定了张素-2的新型相互作用伙伴,扩大了我们对其细胞功能的理解.
- 素-2参与调节细胞能量代谢,将细胞粘附与糖解联系起来.
- 这些发现表明tensin-2是涉及异常细胞粘附和代谢的疾病的潜在治疗标.
更多相关视频
11:02A Functional Assay for Gap Junctional Examination; Electroporation of Adherent Cells on Indium-Tin Oxide
Published on: October 18, 2014
9.9K
08:04Isolation of Primary Mouse Hepatocytes for Nascent Protein Synthesis Analysis by Non-radioactive L-azidohomoalanine Labeling Method
Published on: October 23, 2018
18.8K
相关概念视频
PI3K/mTOR/AKT Signaling Pathway
3.4K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.4K
Interactions Between Signaling Pathways
6.2K
Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
6.2K
The JAK-STAT Signaling Pathway
8.7K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
8.7K
cAMP-dependent Protein Kinase Pathways
6.2K
Cyclic Adenosine Monophosphate (cAMP) is an essential second messenger that activates protein kinase A (PKA) and regulates various biological processes. A single epinephrine molecule binds to GPCR and activates several heterotrimeric G proteins, each stimulating multiple adenylyl cyclase, amplifying the signal, and synthesizing large numbers of cAMP molecules. Small changes in cAMP concentration affect PKA activity. The binding of four cAMP molecules induces a conformational change in PKA,...
6.2K
TGF - β Signaling Pathway
7.3K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
7.3K
Amplifying Signals via Enzymatic Cascade
8.4K
When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
8.4K
