Whether olfaction recognizes odorants by their shape, their molecular vibrations, or both remains an open and controversial question. A convenient way to address it is to test for odor character differences between deuterated and undeuterated odorant isotopomers, since these have identical ground-state conformations but different vibrational modes. In a previous paper (Franco et al. (2011) Proc Natl Acad Sci USA 108:9, 3797-802) we showed that fruit flies can recognize the presence of deuterium in odorants by a vibrational mechanism. Here we address the question of whether humans too can distinguish deuterated and undeuterated odorants. A previous report (Keller and Vosshall (2004) Nat Neurosci 7:4, 337-8) indicated that naive subjects are incapable of distinguishing acetophenone and d-8 acetophenone. Here we confirm and extend those results to trained subjects and gas-chromatography [GC]-pure odorants. However, we also show that subjects easily distinguish deuterated and undeuterated musk odorants purified to GC-pure standard. These results are consistent with a vibrational component in human olfaction.
Block et al. (1) have written a critique of the vibrational theory of olfaction that rests on two main points: (i) they report negative results (i.e., identical responses to normal and deuterated musk isotopomers) in a cultured human embryonic kidney cell derivative line expressing heterologous olfactory receptors; and (ii) they claim that our previous report (2) that humans can smell the difference between undeuterated and deuterated musk isotopomers is in error because of a contaminating impurity they suggest is responsible for the smell difference. We wish to answer these points.Block et al. (1) graciously made the primary data of the musk receptor screen (depicted in figure S3.1 of ref. 1) available to us. We ran an unpaired t test on the entire receptor repertoire and found two (296 and 173 in their numbering) that showed differences between H and D isotopomers. Receptor 296 is their OR51E1, which "was determined to be a nonresponsive OR [odorant receptor] in the follow-up confirmation experiments due to a high receptor background" (1). Its larger response to deuterated isotopomers was not mentioned. Receptor 173 was not described in Block et al.'s paper at all. Its response ( Fig. 1) to D24 and D28 musks was smaller (P < 0.02) than to H and the response to D4 was intermediate. We urge Block et al. to publish the identity of receptor 173 and to reexamine these two receptors that potentially invalidate the main conclusion of their paper.Block et al. (1) assert that an impurity may have affected the odor of our deuterated musks. The peak in our NMR spectra, which they point to, is likely to be caused by a small fraction of cyclopentadecane. Block et al. describe the same impurity in their synthesis, and it is visible in their NMR spectra (figure S2.6 of ref. 1) at 0.87. This impurity does not coelute with the musk and is shown and correctly labeled in figure 2 of ref. 2. Furthermore, our sham deuteration protocol controlled for this. We therefore remain entirely confident that the difference in smell between isotopomers revealed by our doubleblind trials is because of the pure peak of deuterated musk.We are struck by the omission of any description of odor character of the deuterated musks Block et al.(1) synthesized and tested. One assumes that a paper entitled "Implausibility of the vibrational theory of olfaction" would have made use of this information if the isotopes smelled identical.Block et al. (1) assert that deuteration affects many physicochemical properties of odorants. This assertion should be contrasted with their report that in all 14 dose-response curves shown, the affinity of the receptors for deuterated odorants was indistinguishable from that of the hydrogen counterparts. Their results show convincingly that those properties of odorants that are involved in molecular recognition (and therefore in shape theories of olfaction) are left unaltered by deuteration. How then do flies (3), humans (2), and possibly their receptors 173 and 296 detect isotopes?On balance, we feel that Block et al.'s ...
Whether olfaction recognizes odorants by their shape, their molecular vibrations, or both remains an open and controversial question. A convenient way to address it is to test for odor character differences between deuterated and undeuterated odorant isotopomers, since these have identical ground-state conformations but different vibrational modes. In a previous paper Proc Natl Acad Sci USA 108:9, 3797-802) we showed that fruit flies can recognize the presence of deuterium in odorants by a vibrational mechanism. Here we address the question of whether humans too can distinguish deuterated and undeuterated odorants. A previous report (Keller and Vosshall (2004) Nat Neurosci 7:4, 337-8) indicated that naive subjects are incapable of distinguishing acetophenone and d-8 acetophenone. Here we confirm and extend those results to trained subjects and gas-chromatography [GC]-pure odorants. However, we also show that subjects easily distinguish deuterated and undeuterated musk odorants purified to GC-pure standard. These results are consistent with a vibrational component in human olfaction.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.