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人源 T1R3 的富含半胱氨酸结构域是甜味蛋白 thaumatin 与人源 T1R2-T1R3 甜味受体相互作用所必需的。

The cysteine-rich domain of human T1R3 is necessary for the interaction between human T1R2-T1R3 sweet receptors and a sweet-tasting protein, thaumatin.

机构信息

Department of Natural Resources, Graduate School of Global and Environmental Studies, Kyoto University, Japan.

出版信息

Biochem Biophys Res Commun. 2011 Mar 18;406(3):435-8. doi: 10.1016/j.bbrc.2011.02.063. Epub 2011 Feb 15.

Abstract

Thaumatin is an intensely sweet-tasting protein perceived by humans but not rodents. Its threshold value of sweetness in humans is 50nM, the lowest of any sweet-tasting protein. In the present study, the sites where sweet receptors interact with thaumatin were investigated using human embryonic kidney 293 (HEK293) cells expressing the sweet receptors T1R2-T1R3. Chimeric human- mouse sweet receptors were constructed and their responses to sweeteners were investigated. The human (h) T1R2- mouse (m) T1R3 combination responded to sucralose but not to thaumatin, clearly indicating that a T1R3 subunit from humans is necessary for the interaction with thaumatin. Furthermore, results obtained from using chimeric T1R3s showed that the cysteine-rich domain (CRD) of human T1R3 is important for the interaction with thaumatin. The CRD of T1R3 would be a prominent target for designing new sweeteners.

摘要

硫氧还蛋白是一种人类能够感知到的强烈甜味蛋白,但啮齿类动物却不能。它在人类中的甜度阈值为 50nM,是所有具有甜味的蛋白质中最低的。在本研究中,使用表达甜味受体 T1R2-T1R3 的人胚肾 293(HEK293)细胞研究了甜味受体与硫氧还蛋白相互作用的部位。构建了人-鼠嵌合甜味受体,并研究了它们对甜味剂的反应。人(h)T1R2-鼠(m)T1R3 组合对三氯蔗糖有反应,但对硫氧还蛋白没有反应,这清楚地表明与硫氧还蛋白相互作用需要来自人类的 T1R3 亚基。此外,使用嵌合 T1R3 获得的结果表明,人 T1R3 的富含半胱氨酸结构域(CRD)对于与硫氧还蛋白的相互作用很重要。T1R3 的 CRD 将是设计新型甜味剂的重要目标。

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