Bioelectronic Tongue for Identifying and Masking Bitterness Based on Bitter Taste Receptor Agonism and Antagonism

Author:

Hwang Jun Young1,Kim Kyung Ho23ORCID,Seo Sung Eun34ORCID,Nam Youngju1,Jwa Sanghee1,Yang Inwoo1,Park Tai Hyun5,Kwon Oh Seok67ORCID,Lee Seung Hwan1ORCID

Affiliation:

1. Department of Bionano Engineering Center for Bionano Intelligence Education and Research Hanyang University 15588 Ansan Republic of Korea

2. Immunotherapy Research Center Korea Research Institute of Bioscience and Biotechnology (KRIBB) Daejeon 34141 Republic of Korea

3. Infectious Disease Research Center Korea Research Institute of Bioscience and Biotechnology (KRIBB) 34141 125 Gwahak‐ro, Yuseong‐gu Daejeon Republic of Korea

4. Department of Civil and Environmental Engineering Yonsei University Seoul 03722 Republic of Korea

5. Department of Nutritional Science and Food Management Ewha Womans University 03760 Seoul Republic of Korea

6. SKKU Advanced Institute of Nanotechnology (SAINT) Department of Nano Engineering Sungkyunkwan University 16419 Suwon Republic of Korea

7. Department of Nano Science and Technology Sungkyunkwan University 16419 Suwon Republic of Korea

Abstract

AbstractBitterness elicits unpleasant sensations in humans, which can hinder the acceptance of foods and medication adherence. Therefore, identifying and masking bitter tastes is crucial for developing palatable foods and promoting medication compliance in the food and pharmaceutical industries. To achieve this, employing agonism and antagonism of bitter taste receptors as effective strategies at the molecular level is essential. In this study, a bioelectronic tongue is developed to characterize the agonism and antagonism of bitter taste receptors. The human bitter taste receptors hTAS2R16 and hTAS2R31 are produced using an Escherichia coli expression system and reconstituted into nanodiscs (NDs). Subsequently, hTAS2R16‐ and hTAS2R31‐NDs are immobilized on the surface of graphene field‐effect transistors (FETs) to construct bioelectronic tongues. The developed system sensitively detected the bitter agonists, salicin and saccharin, at concentrations as low as 100 fM, with high selectivity in real‐time. The dose‐dependent curves shifted and K values decreased by the antagonists of hTAS2R16 and hTAS2R31, indicating antagonism‐based masking of bitter taste. Therefore, the developed bioelectronic tongue holds promise for identifying bitter tastes and evaluating the masking of bitterness based on the agonism and antagonism of hTAS2Rs.

Funder

Ministry of Education

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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