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甜味增强剂的分子机制。

Molecular mechanism of the sweet taste enhancers.

机构信息

Senomyx, Inc, San Diego, CA 92121, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Mar 9;107(10):4752-7. doi: 10.1073/pnas.0911660107. Epub 2010 Feb 19.

Abstract

Positive allosteric modulators of the human sweet taste receptor have been developed as a new way of reducing dietary sugar intake. Besides their potential health benefit, the sweet taste enhancers are also valuable tool molecules to study the general mechanism of positive allosteric modulations of T1R taste receptors. Using chimeric receptors, mutagenesis, and molecular modeling, we reveal how these sweet enhancers work at the molecular level. Our data argue that the sweet enhancers follow a similar mechanism as the natural umami taste enhancer molecules. Whereas the sweeteners bind to the hinge region and induce the closure of the Venus flytrap domain of T1R2, the enhancers bind close to the opening and further stabilize the closed and active conformation of the receptor.

摘要

人类甜味受体的正变构调节剂已被开发为一种减少饮食中糖摄入量的新方法。除了潜在的健康益处外,甜味增强剂还是研究 T1R 味觉受体的正变构调节一般机制的有价值的工具分子。通过嵌合受体、突变和分子建模,我们揭示了这些甜味增强剂在分子水平上的作用机制。我们的数据表明,甜味增强剂遵循与天然鲜味增强剂分子相似的机制。甜味剂结合在铰链区域并诱导 T1R2 的 Venus flytrap 结构域关闭,而增强剂结合在接近开口的位置,并进一步稳定受体的关闭和激活构象。

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