Cai Chenggu, Jiang Hua, Li Lei, Liu Tianming, Song Xuejie, Liu Bo
Department of Bioengineering, Qilu University of Technology, Jinan, Shandong, 250353, P.R. China.
Department of Food Science and Engineering, Qilu University of Technology, Jinan, Shandong, 250353, P.R. China.
PLoS One. 2016 Aug 1;11(8):e0160079. doi: 10.1371/journal.pone.0160079. eCollection 2016.
Sweet state is a basic physiological sensation of humans and other mammals which is mediated by the broadly acting sweet taste receptor-the heterodimer of Tas1r2 (taste receptor type 1 member 2) and Tas1r3 (taste receptor type 1 member 3). Various sweeteners interact with either Tas1r2 or Tas1r3 and then activate the receptor. In this study, we cloned, expressed and functionally characterized the taste receptor Tas1r2 from a species of Old World monkeys, the rhesus monkey. Paired with the human TAS1R3, it was shown that the rhesus monkey Tas1r2 could respond to natural sugars, amino acids and their derivates. Furthermore, similar to human TAS1R2, rhesus monkey Tas1r2 could respond to artificial sweeteners and sweet-tasting proteins. However, the responses induced by rhesus monkey Tas1r2 could not be inhibited by the sweet inhibitor amiloride. Moreover, we found a species-dependent activation of the Tas1r2 monomeric receptors of human, rhesus monkey and squirrel monkey but not mouse by an intense sweetener perillartine. Molecular modeling and sequence analysis indicate that the receptor has the conserved domains and ligand-specific interactive residues, which have been identified in the characterized sweet taste receptors up to now. This is the first report of the functional characterization of sweet taste receptors from an Old World monkey species.
甜味是人类和其他哺乳动物的一种基本生理感觉,它由广泛作用的甜味受体介导,该受体是Tas1r2(味觉受体1型成员2)和Tas1r3(味觉受体1型成员3)的异二聚体。各种甜味剂与Tas1r2或Tas1r3相互作用,进而激活该受体。在本研究中,我们克隆、表达了一种旧世界猴——恒河猴的味觉受体Tas1r2,并对其进行了功能表征。与人类TAS1R3配对时,结果表明恒河猴Tas1r2能够对天然糖类、氨基酸及其衍生物做出反应。此外,与人类TAS1R2相似,恒河猴Tas1r2能够对人工甜味剂和甜味蛋白做出反应。然而,恒河猴Tas1r2诱导的反应不能被甜味抑制剂氨氯吡脒抑制。此外,我们发现一种强效甜味剂紫苏葶能激活人类、恒河猴和松鼠猴的Tas1r单体受体,但不能激活小鼠的。分子建模和序列分析表明,该受体具有保守结构域和配体特异性相互作用残基,这些在目前已表征的甜味受体中已得到确认。这是关于旧世界猴物种甜味受体功能表征的首次报道。