1. Functional molecular switches of mammalian G protein-coupled bitter-taste receptors.
- Author
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Topin J, Bouysset C, Pacalon J, Kim Y, Rhyu MR, Fiorucci S, and Golebiowski J
- Subjects
- Amino Acid Sequence, Humans, Mutagenesis, Site-Directed, Protein Conformation, Receptors, G-Protein-Coupled chemistry, Receptors, G-Protein-Coupled genetics, Mutation, Receptors, G-Protein-Coupled metabolism, Taste physiology
- Abstract
Bitter taste receptors (TAS2Rs) are a poorly understood subgroup of G protein-coupled receptors (GPCRs). The experimental structure of these receptors has yet to be determined, and key-residues controlling their function remain mostly unknown. We designed an integrative approach to improve comparative modeling of TAS2Rs. Using current knowledge on class A GPCRs and existing experimental data in the literature as constraints, we pinpointed conserved motifs to entirely re-align the amino-acid sequences of TAS2Rs. We constructed accurate homology models of human TAS2Rs. As a test case, we examined the accuracy of the TAS2R16 model with site-directed mutagenesis and in vitro functional assays. This combination of in silico and in vitro results clarifies sequence-function relationships and proposes functional molecular switches that encode agonist sensing and downstream signaling mechanisms within mammalian TAS2Rs sequences., (© 2021. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
- Published
- 2021
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