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Biological Chemistry

Smell Receptors Sniff Out An Aldehyde In Its Hydrated Form

Olfaction: Some odorant receptors bind to aldehydes as geminal diols, a structure found in a nose’s moist environment

by Louisa Dalton
September 17, 2014

Wet Aldehydes
Equilibration scheme between octanal and its geminal diol.
In water, octanal (left) equilibrates with its gem-diol form, octane-1,1-diol (right). Some aldehyde-specific odorant receptors may bind similar scent molecules in the hydrated form.

A rat cruising for dinner will undoubtedly sniff out aldehydes, common odorant molecules in foods and fragrances. But the chemical details of how rodent or other mammalian odorant receptors bind aldehydes are not well understood. Now scientists have discovered a new aspect of this process: Some odorant receptors recognize an aldehyde via its hydrated geminal diol form, which is different from the volatile carbonyl form (ACS Chem. Biol. 2014, DOI: 10.1021/cb400290u). The work suggests that some mammalian olfactory receptors depend on a watery carbonyl-to-diol conversion to sense aldehydes.

When an odorous aldehyde wafts through the air and lands in the nose’s watery mucus, it starts to waffle. In water, an aldehyde equilibrates between its carbonyl form and its hydrated, double hydroxyl version—a gem-diol. The two structures, says Kevin Ryan of the City College of New York, differ dramatically in shape and hydrogen-bonding capability. Yet both forms exist in moist mucus, so he wondered if any of the numerous aldehyde odorant receptors detected the hydrated form.

Ryan and his colleagues, including Stuart Firestein of Columbia University, suspected the answer would vary from one receptor to another. Odorant receptors that bind a diverse range of molecules probably wouldn’t discriminate on the basis of such a structural difference. But the researchers thought that receptors narrowly tuned to recognize only aldehydes might prefer the diol form.

To investigate the question, Ryan and Firestein decided to look at the gem-diol form of octanal, a citrusy aldehyde found in butter, oranges, and rice. However, octanal in water converts from the carbonyl to the diol form and back again, making it difficult to study the diol form on its own. So they made a fluorinated version, 2,2-difluorooctanal. This fluorinated aldehyde strongly favors the diol form when in water because of the electron withdrawing fluorines.

Then they tested the fluorinated compound on 24 odorant receptors that were activated only by aldehydes. About 40% of those receptors responded to 2,2-difluorooctanal, demonstrating that the gem-diol structure is one way that olfactory neurons respond to aldehydes, Ryan says.

Ryan’s group also collaborated with computational chemists at Hebrew University, in Jerusalem, to model a well-studied rodent odorant receptor called OR-I7. When they docked the gem-diol of octanal inside the receptor’s binding site, they found two tyrosines that could simultaneously hydrogen-bond with the gem-diol but not the carbonyl form. “It’s a structural hypothesis for future work,” Ryan says.

The experimental finding is especially important for computational modelers, says Hanns Hatt of Ruhr University Bochum, in Germany. With no hard structural data from X-ray crystallography yet available, many of the models of aldehyde odorant receptors created in the past few years have not considered the gem-diol as a ligand; he thinks future studies likely will.



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