The structure of human sweetness

Cell. 2025 Jul 24;188(15):4141-4153.e18. doi: 10.1016/j.cell.2025.04.021. Epub 2025 May 7.

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.

Keywords: GPCR; cryo-EM; human; sensory biology; structure; sweet receptor; sweeteners; taste.

MeSH terms

  • Aspartame / chemistry
  • Aspartame / metabolism
  • Cryoelectron Microscopy
  • Humans
  • Models, Molecular
  • Receptors, G-Protein-Coupled* / chemistry
  • Receptors, G-Protein-Coupled* / metabolism
  • Receptors, G-Protein-Coupled* / ultrastructure
  • Sucrose / analogs & derivatives
  • Sucrose / chemistry
  • Sucrose / metabolism
  • Sweetening Agents* / chemistry
  • Sweetening Agents* / metabolism
  • Taste
  • Taste Buds / metabolism
  • Taste Receptors, Type 2

Substances

  • Sweetening Agents
  • Receptors, G-Protein-Coupled
  • Sucrose
  • Aspartame
  • trichlorosucrose
  • Taste Receptors, Type 2