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Identification of Ligands for two human bitter T2R receptors

机译:鉴定两个人类苦味T2R受体的配体

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摘要

Earlier, a family of G protein-coupled receptors, termed T2Rs, was identified in the rodent and human genomes through data mining. It was suggested that these receptors mediate bitter taste perception. Analysis of the human genome revealed that the hT2R family is composed of 25 members. However, bitter ligands have been identified for only three human receptors so far. Here we report identification of two novel ligand-receptor pairs. hT2R61 is activated by 6-nitrosaccharin, a bitter derivative of saccharin. hT2R44 is activated by denatonium and 6-nitrosaccharin. Activation profiles for these receptors correlate with psychophysical data determined for the bitter compounds in human studies. Functional analysis of hT2R chimeras allowed us to identify residues in extracellular loops critical for receptor activation by ligands. The discovery of two novel bitter ligand-receptor pairs provides additional support for the hypothesis that hT2Rs mediate a bitter taste response in humans.
机译:早期,通过数据挖掘在啮齿动物和人类基因组中鉴定了一个称为T2R的G蛋白偶联受体家族。提示这些受体介导苦味觉。对人类基因组的分析表明,hT2R家族由25个成员组成。然而,迄今为止,仅针对三种人类受体鉴定了苦配体。在这里,我们报告鉴定两个新的配体-受体对。 hT2R61被6-亚糖精(糖精的苦味衍生物)激活。 hT2R44被地那铵和6-亚硝基糖精激活。这些受体的激活特征与人类研究中针对苦味化合物确定的心理物理学数据相关。 hT2R嵌合体的功能分析使我们能够识别细胞外环中对配体激活受体至关重要的残基。两个新颖的苦配体-受体对的发现为hT2Rs介导人的苦味反应的假设提供了额外的支持。

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