Rational tuning of temperature sensitivity in TRPM8 channel

ABSTRACT: Detecting temperature is crucial for the survival of living organisms. Although the temperature sensitive Transient Receptor Potential Melastatin 8 (TRPM8) channel has been identified as the prototypical cold sensor, the mechanisms by which it detects temperature remain elusive. In this study, we first identified groups of clustered residues that undergo conformational rearrangements between buried and exposed states during cold activation by hydroxyl radical footprinting-mass spectrometry (HRF-MS). By systematically perturbing water-protein interactions at these residues with point mutations that changes in the side chain hydrophobicity (SCH), we achieved rational tuning of temperature sensitivity in this channel. Specifically, mutations with the clearest impacts on TRPM8 cold sensitivity

SUBMITTER: Lizhen Xu 

PROVIDER: S-SCDT-10_1038-S44319-025-00630-2 | biostudies-other |

REPOSITORIES: biostudies-other