将GAP与激活的PDGF受体结合在一起
A Kazlauskas1, C Ellis, T Pawson
1Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
概括
血小板衍生生长因子 (PDGF) 信号传递涉及Ras GTPase激活蛋白 (GAP). 结合其受体的PDGF招募了GAP,需要受体激酶活性和特定的氨酸酸化位点才能获得最大的关联.
科学领域:
- 细胞信号通道是细胞信号通道.
- 分子生物学分子生物学
- 瘤基因研究研究
背景情况:
- 拉斯原型瘤基因产品是细胞内关键信号转换器.
- 拉斯GTPase激活蛋白 (GAP) 调解了来自拉斯的信号.
- 血小板衍生生长因子 (PDGF) 受体在结合联体时启动信号级联.
研究的目的:
- 为了研究PDGF受体和GAP之间的相互作用.
- 阐明GAP与PDGF受体结合的分子要求.
主要方法:
- 利用狗的上皮细胞进行工程,以表达人类PDGF受体.
- 研究了PDGF结合对GAP复合体形成的影响.
- 使用突变的PDGF受体来识别受体-GAP关联的关键领域和活动.
主要成果:
- 在约10%的总GAP分子中,PDGF结合诱导了GAP和PDGF受体之间的复合形成.
- GAP与受体的最大关联需要活性受体激酶功能.
- 在自酸化部位的特定可酸化的氨酸残留物对于强大的GAP复杂化至关重要.
结论:
- PDGF受体和GAP之间的相互作用是PDGF介导的细胞内信号传递的关键步骤.
- 受体激酶活性和特定的铁酸化位点对于有效招募GAP是不可或缺的.
- 这种相互作用突出了由生长因子受体对Ras信号通路的复杂调节.
相关概念视频
Amplifying Signals via Second Messengers
Many receptor binding ligands are hydrophilic; they do not cross the cell membrane but bind to cell-surface receptors. Thus, their message must be relayed by second messengers present in the cell cytoplasm. There are several second messenger pathways, each with its own way of relaying information. For example, the G protein-coupled receptors can activate both phosphoinositol and cyclic AMP (cAMP) second messenger pathways. The phosphoinositol pathway is active when the receptor induces...
Amplifying Signals via Enzymatic Cascade
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 the...
Activation and Inactivation of G Proteins
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high affinity and are together...
GPCR Desensitization
G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
GPCRs Regulate Adenylyl Cylase Activity
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of cells.
Two...
Two...
IP3/DAG Signaling Pathway
Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and produces two-second...


