Probing the Binding Pocket of the Broadly Tuned Human Bitter Taste Receptor TAS2R14 by Chemical Modification of Cognate Agonists

Authors

  • Rafik Karaman,

    1. Bioorganic Chemistry Department, Faculty of Pharmacy, Al-Quds University, Jerusalem, Israel
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  • Stefanie Nowak,

    1. Department of Molecular Genetics, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
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    • Authors contributed equally.
  • Antonella Di Pizio,

    1. The Institute of Biochemistry, Food and Nutrition, The Robert H Smith Faculty of Agriculture, Food and Environment, The Hebrew University, Rehovot, Israel
    2. The Fritz Haber Center for Molecular Dynamics, The Hebrew University, Jerusalem, Israel
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    • Authors contributed equally.
  • Hothaifa Kitaneh,

    1. Bioorganic Chemistry Department, Faculty of Pharmacy, Al-Quds University, Jerusalem, Israel
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  • Alaa Abu-Jaish,

    1. Bioorganic Chemistry Department, Faculty of Pharmacy, Al-Quds University, Jerusalem, Israel
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  • Wolfgang Meyerhof,

    1. Department of Molecular Genetics, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
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  • Masha Y. Niv,

    1. The Institute of Biochemistry, Food and Nutrition, The Robert H Smith Faculty of Agriculture, Food and Environment, The Hebrew University, Rehovot, Israel
    2. The Fritz Haber Center for Molecular Dynamics, The Hebrew University, Jerusalem, Israel
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  • Maik Behrens

    Corresponding author
    1. Department of Molecular Genetics, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany
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Abstract

Sensing potentially harmful bitter substances in the oral cavity is achieved by a group of ˜25 receptors, named TAS2Rs, which are expressed in specialized sensory cells and recognize individual but overlapping sets of bitter compounds. The receptors differ in their tuning breadths ranging from narrowly to broadly tuned receptors. One of the most broadly tuned human bitter taste receptors is the TAS2R14 recognizing an enormous variety of chemically diverse synthetic and natural bitter compounds, including numerous medicinal drugs. This suggests that this receptor possesses a large readily accessible ligand binding pocket. To allow probing the accessibility and size of the ligand binding pocket, we chemically modified cognate agonists and tested receptor responses in functional assays. The addition of large functional groups to agonists was usually possible without abolishing agonistic activity. The newly synthesized agonist derivatives were modeled in the binding site of the receptor, providing comparison to the mother substances and rationalization of the in vitro activities of this series of compounds.

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