Waterloo Lukas A W, Löber Stefan, Gmeiner Peter
Newcastle University, United Kingdom.
Department of Chemistry and Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91058 Erlangen.
Chimia (Aarau). 2022 May 25;76(5):418-424. doi: 10.2533/chimia.2022.418.
G protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants. Besides human senses like vision and olfaction, taste perception is mostly mediated by GPCRs. Hence, the bitter taste receptor family TAS2R comprises 25 distinct receptors and plays a key role in food acceptance and drug compliance. The TAS2R14 subtype is the most broadly tuned bitter taste receptor, recognizing a range of chemically highly diverse agonists. Besides other tissues, it is expressed in human airway smooth muscle and may represent a novel drug target for airway diseases. Several natural products as well as marketed drugs including flufenamic acid have been identified to activate TAS2R14, but higher potency ligands are needed to investigate the ligand-controlled physiological function and to facilitate the targeted modulate for potential future clinical applications. A combination of structure-based molecular modeling with chemical synthesis and in vitro profiling recently resulted in new flufenamic acid agonists with improved TAS2R14 potency and provided a validated and refined structural model of ligand-TAS2R14 interactions, which can be applied for future drug design projects.
G蛋白偶联受体(GPCRs)介导了我们对激素、神经递质和环境刺激的大部分生理反应。除了视觉和嗅觉等人类感官外,味觉感知大多也由GPCRs介导。因此,苦味受体家族TAS2R包含25种不同的受体,在食物接受和药物依从性方面发挥着关键作用。TAS2R14亚型是调谐范围最广的苦味受体,能识别一系列化学性质高度多样的激动剂。除了其他组织外,它还在人气道平滑肌中表达,可能是气道疾病的新型药物靶点。已确定几种天然产物以及包括氟芬那酸在内的上市药物可激活TAS2R14,但需要更高效的配体来研究配体控制的生理功能,并促进针对潜在未来临床应用的靶向调节。基于结构的分子建模与化学合成及体外分析相结合,最近产生了具有更高TAS2R14活性的新型氟芬那酸激动剂,并提供了经过验证和完善的配体-TAS2R14相互作用结构模型,可应用于未来的药物设计项目。