The structure of human sweetness

In humans, the detection and ultimately the perception of sweetness begin in the oral cavity, where taste receptor cells (TRCs) dedicated to sweet-sensing interact with sugars, artificial sweeteners, and other sweet-tasting chemicals. Human sweet TRCs express on their cell surface a sweet receptor that initiates the cascade of signaling events responsible for our strong attraction to sweet stimuli. Here, we describe the cryo-electron microscopy (cryo-EM) structure of the human sweet receptor bound to two of the most widely used artificial sweeteners-sucralose and aspartame. Our results reveal the structural basis for sweet detection, provide insights into how a single receptor mediates all our responses to such a wide range of sweet-tasting compounds, and open up unique possibilities for designing a generation of taste modulators informed by the structure of the human receptor.

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Publication Details

Journal
Cell
Published
2025-05-07
DOI
https://doi.org/10.1016/j.cell.2025.04.021
Citations
45
Primary Topic
Biochemical Analysis and Sensing Techniques
Type
article
Field-Weighted Citation Impact
50.38
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article

The structure of human sweetness

Zhengyuan Lu, Robert K. Yu, B. Wang, Charles S. Zuker et al.
45 citations
Cell
Biochemical Analysis and Sensing Techniques
50.38
article

The structure of human sweetness

Zhengyuan Lu, Robert K. Yu, B. Wang, Charles S. Zuker, Anthony W. P. Fitzpatrick, Zhang Juen, Andrew Chang
article en
45 citations

Abstract

In humans, the detection and ultimately the perception of sweetness begin in the oral cavity, where taste receptor cells (TRCs) dedicated to sweet-sensing interact with sugars, artificial sweeteners, and other sweet-tasting chemicals. Human sweet TRCs express on their cell surface a sweet receptor that initiates the cascade of signaling events responsible for our strong attraction to sweet stimuli. Here, we describe the cryo-electron microscopy (cryo-EM) structure of the human sweet receptor bound to two of the most widely used artificial sweeteners-sucralose and aspartame. Our results reveal the structural basis for sweet detection, provide insights into how a single receptor mediates all our responses to such a wide range of sweet-tasting compounds, and open up unique possibilities for designing a generation of taste modulators informed by the structure of the human receptor.

CellVol. 188(15)
Columbia University (US)
Zero hunger
Openalex Percentile: Top 0%
Biochemical Analysis and Sensing Techniques
50.38
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