Understand spiciness: mechanism of TRPV1 channel activation by capsaicin

Fan Yang, Jie Zheng

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Protein Cell ›› 2017, Vol. 8 ›› Issue (3) : 169-177. DOI: 10.1007/s13238-016-0353-7
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Understand spiciness: mechanism of TRPV1 channel activation by capsaicin

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Abstract

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 simulation. A framework of how capsaicin binds and activates TRPV1 has started to merge: capsaicin binds to a pocket formed by the channel’s transmembrane segments, where it takes a “tail-up, head-down” configuration. Binding is mediated by both hydrogen bonds and van der Waals interactions. Upon binding, capsaicin stabilizes the open state of TRPV1 by “pull-andcontact” with the S4-S5 linker. Understanding the ligand-host interaction will greatly facilitate pharmaceutical efforts to develop novel analgesics targeting TRPV1.

Keywords

capsaicin / TRPV1 / ligand gating / cryo-EM / computation / spiciness

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Fan Yang, Jie Zheng. Understand spiciness: mechanism of TRPV1 channel activation by capsaicin. Protein Cell, 2017, 8(3): 169‒177 https://doi.org/10.1007/s13238-016-0353-7

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