Gating elements for carvacrol activation of the OTOP1 proton channel

• Published in: Communications biology Vol. 7; no. 1; pp. 1106 - 10
• Main Authors: Hu, Jingmei, Han, Yalan, Luo, Anna, Zhang, Hao, Tian, Lifeng, Cai, Huajun, Xue, Beiru, Lai, Ren, Luo, Lei
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 09-09-2024; Nature Publishing Group; Nature Portfolio
• Subjects: 14; 14/34; 38/109; 631/45/269; 631/57; 9/74; Animals; Biology; Biomedical and Life Sciences; Carvacrol; Channel gating; Chimeras; Cymenes - pharmacology; Drug development; Evolution & development; HEK293 Cells; Humans; Hydrogen-Ion Concentration; Investigations; Ion Channel Gating - drug effects; Ion Channels - genetics; Ion Channels - metabolism; Laboratories; Life Sciences; Mice; Peptides; pH effects; Physiology; Point mutation; Protons; Science; Sour taste
• ISSN: 2399-3642; 2399-3642
• DOI: 10.1038/s42003-024-06818-x

Otopetrin 1 (OTOP1) is a proton-activated channel crucial for animals’ perception of sour taste. Despite its significance, the gating mechanism of OTOP1 remains poorly understood. Here, we demonstrate that carvacrol activates the mouse OTOP1 (mOTOP1) channel under neutral and acidic conditions. Functional analysis showed that carvacrol enhances pH fluorescence signals in OTOP1-expressing cells, with reduced efficacy at lower pH levels. Carvacrol selectively activates mOTOP1, while mOTOP2, mOTOP3, and
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OTOP1 (CmOTOP1) are insensitive to carvacrol activation under neutral pH. Through chimera and point mutation experiments, swapping S134 in transmembrane segment 3 (TM3) and T247 in the TM5-6 linker abolished carvacrol activation of mOTOP1 and conferred activation on CmOTOP1, suggesting these two residues are critical for carvacrol sensitivity. These findings highlight TM3 and TM5-6 linker as pivotal gating apparatus of OTOP1 channels and potential docking sites for drug design.
Carvacrol activates mouse OTOP1 (mOTOP1) at neutral and acidic pH, but not other OTOPs. Key residues S134 and T247 are critical for carvacrol sensitivity, highlighting TM3 and TM5-6 linker as crucial for gating and drug design.