相关实验视频
Updated: Jul 9, 2025

07:10
Taste Exam: A Brief and Validated Test
Published on: August 17, 2018
16.5K
作为药物点的苦味受体TAS2R14是一个药物点
Lukas A W Waterloo1, Stefan Löber2, Peter Gmeiner3
1Newcastle University, United Kingdom. lukas.waterloo@ncl.ac.uk.
Chimia
|December 9, 2023
概括
研究人员开发了新的,更强大的苦味受体TAS2R14激动剂. 这一发现有助于对TAS2R14的理解.
科学领域:
- 药理学 药理学是指药理学的学科.
- 分子生物学分子生物学
- 药物发现 药物发现 药物发现
背景情况:
- G蛋白结合受体 (GPCRs) 对于生理反应至关重要,包括味觉感知.
- 苦味受体家族 (TAS2R) 有25个亚型,影响食物接受和药物服药.
- 广泛调节的受体TAS2R14在气道光滑肌中表达,这表明气道疾病治疗的潜力.
研究的目的:
- 为了确定TAS2R14苦味受体的新型,高强度的激动剂.
- 为未来的药物设计完善连接体-TAS2R14相互作用的结构模型.
- 探索TAS2R14作为呼吸道疾病的潜在治疗点.
主要方法:
- 基于结构的分子建模.
- 新型激动剂的化学合成.
- 在体外对联体受体相互作用的分析.
主要成果:
- 鉴定了新的基于胺酸的激动剂,具有增强的TAS2R14强度.
- 开发一种经过验证和完善的连接体-TAS2R14相互作用的结构模型.
- 证明了对TAS2R14的改进联结体功效的证明.
结论:
- 开发了具有强度提高的新型TAS2R14激动剂.
- 一个精细的结构模型促进了未来的药物设计,以TAS2R14为目标.
- TAS2R14代表了新型治疗策略的有希望的目标,特别是在呼吸道疾病中.
相关概念视频
The Physiology of Taste
3.9K
The perception of a salty flavor is facilitated by sodium ions within the oral salivary fluid. Upon consumption of a salty substance, salt crystals disassemble, leading to the liberation of its constituents—Na+ and Cl- ions. These ions subsequently dissolve into the salivary fluid present in the oral cavity. The external environment of the gustatory cells experiences an elevation in Na+ concentration, thereby establishing a potent concentration gradient. This gradient propels the...
3.9K
Gustation
48.1K
Gustation is a chemical sense that, along with olfaction (smell), contributes to our perception of taste. It starts with the activation of receptors by chemical compounds (tastants) dissolved in the saliva. The saliva and filiform papillae on the tongue distribute the tastants and increase their exposure to the taste receptors.
48.1K
Taste Buds and Receptors
2.0K
Gustation, or the sense of taste, is intrinsically linked to the anatomical structures located on the tongue. This organ's surface, along with the entirety of the oral cavity, is adorned with stratified squamous epithelium. Evident on the tongue are elevated structures known as papillae (singular = papilla), which house the mechanisms for the transduction of gustatory stimuli. Four distinct types of papillae exist, each identified by their unique morphological attributes: the circumvallate,...
2.0K
G Protein-coupled Receptors
12.1K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
12.1K
G-Protein Gated Ion Channels
4.6K
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...
4.6K
Drug-Receptor Interaction: Agonist
2.5K
Agonists are drugs that interact with specific receptors in the body to produce a biological response. When an agonist binds to a receptor, it activates or enhances the receptor's function, leading to physiological effects. The interaction between agonist drugs and receptors is crucial for their therapeutic action in various medical treatments.
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous...
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous...
2.5K

