6o72 | pdb_00006o72

Structure of the TRPM8 cold receptor by single particle electron cryo-microscopy, TC-I 2014-bound state

spinqualitylabelsall models 6o72, resolution 3.00Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 6o72 is a 4 chain structure with sequence from Great tit. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: 9PE, NA, T14, UND, Y01 Related: 6o6r, 6o77, 6o6a Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Publication Abstract from PubMed The transient receptor potential melastatin 8 (TRPM8) ion channel is the primary detector of environmental cold and an important target for treating pathological cold hypersensitivity. Here, we present cryo-electron microscopy structures of TRPM8 in ligand-free, antagonist-bound, or calcium-bound forms, revealing how robust conformational changes give rise to two nonconducting states, closed and desensitized. We describe a malleable ligand-binding pocket that accommodates drugs of diverse chemical structures, and we delineate the ion permeation pathway, including the contribution of lipids to pore architecture. Furthermore, we show that direct calcium binding mediates stimulus-evoked desensitization, clarifying this important mechanism of sensory adaptation. We observe large rearrangements within the S4-S5 linker that reposition the S1-S4 and pore domains relative to the TRP helix, leading us to propose a distinct model for modulation of TRPM8 and possibly other TRP channels. Structural insights into TRPM8 inhibition and desensitization.,Diver MM, Cheng Y, Julius D Science. 2019 Sep 27;365(6460):1434-1440. doi: 10.1126/science.aax6672. Epub 2019, Sep 5. PMID:31488702 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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