# Beef-Derived Peptides Mediated Desensitization of Bitter Taste Receptor T2R14 Through GPCR Kinase 2

**Authors:** Nisha Singh, Julia Drube, Carsten Hoffmann, Rotimi Emmanuel Aluko, Prashen Chelikani

PMC · DOI: 10.3390/nu18060901 · Nutrients · 2026-03-12

## TL;DR

Beef-derived peptides can block bitter taste receptor T2R14 and speed up its signal shutdown via GRK2, potentially improving the taste of bitter foods and medicines.

## Contribution

Discovery that beef peptides inhibit T2R14 and mediate its desensitization through GRK2, expanding their potential use in food and medicine.

## Key findings

- AGDDAPRAVF and ETSARHL peptides significantly inhibit T2R14 activity.
- GRK2 knockout reduces calcium release and delays desensitization in T2R14-expressing cells.
- Beef peptides do not significantly affect cAMP levels in T2R14 signaling.

## Abstract

Background/Objectives: Humans have at least 26 bitter taste receptors (T2Rs), and among these, bitter taste receptor 14 (T2R14) is highly expressed in both oral and extraoral tissues. Over 100 bitter ligands can activate T2R14, including hormones, vitamins, plant compounds, and peptides. Previous studies suggest that bitter tastants such as quinine and caffeine can inhibit G protein-coupled receptor kinases (GRKs) and delay T2R signal termination. Our earlier research showed that peptides from alcalase and chymotrypsin hydrolysates of beef proteins inhibited quinine-dependent calcium release through T2R4, with AGDDAPRAVF and ETSARHL showing the greatest effectiveness. However, the effect of these antagonistic peptides on other T2Rs, such as T2R14 signaling, remains unknown. This study aimed to evaluate the ability of these beef protein-derived peptides to activate or inhibit T2R14 signaling and the involvement of GRK2 in signal termination. Methods and Results: Our results indicate that the above two antagonist peptides significantly inhibit T2R14 activity. Furthermore, GRK2 knockout in HEK cells stably expressing T2R14 decreases intracellular calcium release, as measured by the area under the curve (AUC), and also delays the fall time (indication of desensitization) of the calcium response when exposed to the T2R14 agonist diphenhydramine (DPH) or beef protein-derived agonist peptide TMTL. Next, we measured the effects of these ligands on cAMP accumulation, and our results suggest no significant change in cAMP levels upon treatment with beef protein-derived peptides. Conclusions: Thus, this study showed that beef protein-derived peptides can function as both T2R inhibitors and mediate T2R14 desensitization through GRK2 signaling. These antagonistic food protein-derived peptides inform strategies to enhance nutrition, such as promoting healthier food choices by reducing bitterness and thereby improving the palatability of health-promoting bitter foods, such as fruit and vegetable extracts, as well as bitter medications.

## Linked entities

- **Genes:** TAS2R14 (taste 2 receptor member 14) [NCBI Gene 50840], GRK2 (G protein-coupled receptor kinase 2) [NCBI Gene 156]
- **Chemicals:** quinine (PubChem CID 441073), caffeine (PubChem CID 2519), diphenhydramine (PubChem CID 3100)

## Full-text entities

- **Genes:** TAS2R14 (taste 2 receptor member 14) [NCBI Gene 50840] {aka T2R14, TRB1}, GRK2 (G protein-coupled receptor kinase 2) [NCBI Gene 156] {aka ADRBK1, BARK1, BETA-ARK1}
- **Chemicals:** quinine (MESH:D011803), calcium (MESH:D002118), caffeine (MESH:D002110), TMTL (-), DPH (MESH:D004155)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029621/full.md

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Source: https://tomesphere.com/paper/PMC13029621