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Tongue-on-a-Chip: Parallel Recording of Sweet and Bitter Receptor Responses to Sequential Injections of Pure and Mixed Sweeteners.
Roelse, Margriet; Krasteva, Nadejda; Pawlizak, Steve; Mai, Michaela K; Jongsma, Maarten A.
Affiliation
  • Roelse M; BU Bioscience, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.
  • Krasteva N; Stuttgart Laboratory 2, Sony Semiconductor Solutions Europe, Sony Europe B.V., Zweigniederlassung Deutschland, Hedelfinger Str. 61, 70327 Stuttgart, Germany.
  • Pawlizak S; Stuttgart Laboratory 2, Sony Semiconductor Solutions Europe, Sony Europe B.V., Zweigniederlassung Deutschland, Hedelfinger Str. 61, 70327 Stuttgart, Germany.
  • Mai MK; Stuttgart Laboratory 2, Sony Semiconductor Solutions Europe, Sony Europe B.V., Zweigniederlassung Deutschland, Hedelfinger Str. 61, 70327 Stuttgart, Germany.
  • Jongsma MA; BU Bioscience, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.
J Agric Food Chem ; 72(28): 15854-15864, 2024 Jul 17.
Article in En | MEDLINE | ID: mdl-38951504
ABSTRACT
A microfluidic tongue-on-a-chip platform has been evaluated relative to the known sensory properties of various sweeteners. Analogous metrics of typical sensory features reported by human panels such as sweet taste thresholds, onset, and lingering, as well as bitter off-flavor and blocking interactions were deduced from the taste receptor activation curves and then compared. To this end, a flow cell containing a receptor cell array bearing the sweet and six bitter taste receptors was transiently exposed to pure and mixed sweetener samples. The sample concentration gradient across time was separately characterized by the injection of fluorescein dye. Subsequently, cellular calcium responses to different doses of advantame, aspartame, saccharine, and sucrose were overlaid with the concentration gradient. Parameters describing the response kinetics compared to the gradient were quantified. Advantame at 15 µM recorded a significantly faster sweetness onset of 5 ± 2 s and a longer lingering time of 39 s relative to sucrose at 100 mM with an onset of 13 ± 2 s and a lingering time of 6 s. Saccharine was shown to activate the bitter receptors TAS2R8, TAS2R31, and TAS2R43, confirming its known off-flavor, whereas addition of cyclamate reduced or blocked this saccharine bitter response. The potential of using this tongue-on-a-chip to bridge the gap with in vitro assays and taste panels is discussed.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sweetening Agents / Taste / Receptors, G-Protein-Coupled Limits: Humans Language: En Journal: J Agric Food Chem Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sweetening Agents / Taste / Receptors, G-Protein-Coupled Limits: Humans Language: En Journal: J Agric Food Chem Year: 2024 Document type: Article