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

被引:28
|
作者
Ohta, Keisuke [1 ]
Masuda, Tetsuya
Tani, Fumito
Kitabatake, Naofumi
机构
[1] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto 6110011, Japan
关键词
Thaumatin; Sweet-tasting protein; Sweet receptor; Cell-based assay; Chimeric human-mouse sweet receptors; AMINO-ACID-SEQUENCE; BINDING-SITES; BRAZZEIN; RESPONSES; NEOCULIN;
D O I
10.1016/j.bbrc.2011.02.063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thaumatin is an intensely sweet-tasting protein perceived by humans but not rodents. Its threshold value of sweetness in humans is 50 nM, 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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:435 / 438
页数:4
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