通过近距离蛋白质学揭示的上腺 CaV1.2刺激的机制
Guoxia Liu1, Arianne Papa2, Alexander N Katchman1
1Division of Cardiology, Department of Medicine, Columbia University, Vagelos College of Physicians and Surgeons, New York, NY, USA.
Nature
|January 24, 2020
概括
研究人员发现蛋白质Rad, 不仅仅是通道本身, 调解战斗或逃跑反应. 蛋白激酶A的酸化缓解了其对CaV1.2通道的抑制,增加了心脏收缩性.
科学领域:
- 分子生物学
- 心血管生理学
- 离子通道规则
背景情况:
- 通过CaV1.2通道增强心脏收缩能力.
- 之前的研究表明非通道因素有助于这种增强.
- 蛋白激酶A (PKA) 是β-上腺体信号的关键媒介.
研究的目的:
- 阐明β-上腺激动剂刺激电压通道的精确机制.
- 为了确定参与CaV的上腺素调节的非通道蛋白因素1.2.
主要方法:
- 使用转基因小鼠心表达甲酸过氧化酶结合的CaV1.2个子单位.
- 采用多重化定量蛋白质学来分析蛋白质与CaV的接近性1.2.
- 研究了PKA酸化对Rad和CaV1. 2之间的相互作用的影响.
主要成果:
- 在CaV1.2微环境中识别了G蛋白Rad.
- 在β-上腺刺激期间观察到Rad耗尽.
- 证明PKA酸化Rad可以降低其对CaV1.2β子单元的亲和力,增加通道开放的概率和缓解抑制.
结论:
- 蛋白质Rad在CaV1.2通道的β-上腺素刺激中起到至关重要的作用.
- 通过PKA调节的Rad酸化对于增加心脏收缩能力至关重要.
- 这种电压通道的上刺激调节机制在进化过程中得到保留,也影响了CaV1.3和CaV2.2.
相关概念视频
GPCRs Regulate Adenylyl Cylase Activity
7.1K
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...
7.1K
Tension Response at Adherens Junctions
3.4K
The adherens junctions that anchor cells together are multi-protein complexes that dynamically adapt to mechanical stimuli such as tensile forces and shear stress. Mechanosensory proteins in these junctions can sense such mechanical stimuli and undergo a shift in their conformation, resulting in an altered function — a process called mechanotransduction.
α-Catenin as a Mechanosensory Protein
The α-catenin of adherens junctions is an allosteric protein with three VH (vinculin...
α-Catenin as a Mechanosensory Protein
The α-catenin of adherens junctions is an allosteric protein with three VH (vinculin...
3.4K
Adrenergic Receptors: β Subtype
3.3K
β-adrenoceptors have varied sensitivities towards adrenaline, noradrenaline, and isoprenaline. The order of agonist potency is as follows:
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors...
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors...
3.3K
G-Protein Gated Ion Channels
5.5K
GPCRs are primarily responsible for our sense of smell, taste, and vision. The binding of a sensory stimulus activates GPCR to stimulate effector proteins, many of which are ion channels in the sensory organs. GPCRs modulate the opening and closing of the target ion channels either directly by binding them, or by releasing second messengers that activate these channels. As ions move across the membrane, the membrane potential is altered, which induces an appropriate response.
Sensory...
Sensory...
5.5K
Adrenergic Receptors: ɑ Subtype
2.6K
Adrenoceptors are classified into α and ꞵ classes based on their potencies to catecholamine agonists. α-adrenoceptors show the following order of catecholamine potency:
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase...
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase...
2.6K
Adrenergic Receptors (Adrenoceptors): Classification
4.4K
Adrenergic receptors, or adrenoceptors, respond to the autonomic neurotransmitter noradrenaline and other endogenous catecholamine agonists. They are classified into two main families, α and β, based on their pharmacological response and are further subdivided depending on their location, elicited response, and affinity to specific agonists or antagonists.
α-Adrenoceptors
α-Adrenoceptors are classified into two main subtypes: α1 and α2. The α1 adrenoceptors,...
α-Adrenoceptors
α-Adrenoceptors are classified into two main subtypes: α1 and α2. The α1 adrenoceptors,...
4.4K


