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

  • Rafik Karaman (Erstautor/-in)
  • , Stefanie Nowak (Co-Autor/-in)
  • , Antonella Di Pizio (Co-Autor/-in)
  • , Hothaifa Kitaneh (Co-Autor/-in)
  • , Alaa Abu-Jaish (Co-Autor/-in)
  • , Wolfgang Meyerhof (Co-Autor/-in)
  • , Masha Y. Niv (Co-Autor/-in)
  • , Maik Behrens* (Letztautor/-in)
  • *Korrespondierende/r Autor/-in für diese Arbeit
  • Al-Quds University
  • DIfE - Deutsches Institut für Ernährungsforschung Potsdam-Rehbrücke
  • Hebräische Universität von Jerusalem

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

55 Zitate (Scopus)

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.

OriginalspracheEnglisch
Seiten (von - bis)66-75
Seitenumfang10
FachzeitschriftChemical Biology and Drug Design
DOIs
PublikationsstatusVeröffentlicht - 1 Juli 2016
Extern publiziertJa

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