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Protein & Cell, 2017-03, Vol.8 (3), p.169-177
2017

Details

Autor(en) / Beteiligte
Titel
Understand spiciness: mechanism of TRPV1 channel activation by capsaicin
Ist Teil von
  • Protein & Cell, 2017-03, Vol.8 (3), p.169-177
Ort / Verlag
Beijing: Higher Education Press
Erscheinungsjahr
2017
Link zum Volltext
Quelle
Electronic Journals Library
Beschreibungen/Notizen
  • Capsaicin in chili peppers bestows the sensation of spiciness. Since the discovery of its receptor, transient receptor potential vanilloid 1 (TRPV1) ion channel, how capsaicin activates this channel has been under extensive investigation using a variety of experimental techniques including mutagenesis, patch-clamp recording, crystallography, cryo-electron microscopy, computational docking and molecular dynamic simu- lation. A framework of how capsaicin binds and acti- vates TRPV1 has started to merge: capsaicin binds to a pocket formed by the channel's transmembrane seg- ments, where it takes a "tail-up, head-down" configu- ration. Binding is mediated by both hydrogen bonds and van der Waals interactions. Upon binding, cap- saicin stabilizes the open state of TRPV1 by "pull-and- contact" with the $4-$5 linker. Understanding the ligand-host interaction will greatly facilitate pharma- ceutical efforts to develop novel analgesics targeting TRPV1.

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