9RGM
SsCl at pH 6.5 - closed
Summary for 9RGM
| Entry DOI | 10.2210/pdb9rgm/pdb |
| EMDB information | 53950 |
| Descriptor | pH gated chloride channel (1 entity in total) |
| Functional Keywords | ion channel, plgic, ph-sensitive channel, membrane protein |
| Biological source | Sarcoptes scabiei |
| Total number of polymer chains | 5 |
| Total formula weight | 200201.33 |
| Authors | Kleiz-Ferreira, J.,Brams, M.,Harrison, P.J.,Gallagher, C.,Nys, M.,Donze, Y.,Quigley, A.,Bertrand, D.,Ulens, C. (deposition date: 2025-06-06, release date: 2026-03-18, Last modification date: 2026-04-22) |
| Primary citation | Kleiz-Ferreira, J.,Brams, M.,Harrison, P.J.,Gallagher, C.I.,Nys, M.,Donze, Y.,Quigley, A.,Bertrand, D.,Ulens, C. Structure of a pH-sensitive pentameric ligand-gated ion channel from the Sarcoptes scabies mite. Nat Commun, 17:-, 2026 Cited by PubMed Abstract: Scabies is a skin infestation caused by the mite Sarcoptes scabiei and represents a substantial global health burden exacerbated by emerging resistance to ivermectin. An anionic pentameric ligand-gated ion channel from the mite, SsCl, shows pH-sensitivity and is significantly modulated by ivermectin. Here, we use cryo-EM and electrophysiology to explore the pH-sensing mechanisms of SsCl and the impact of ivermectin on channel activity. Structures of SsCl were resolved in closed (pH 6.5) and desensitized (pH 9) states, alongside ivermectin-bound conformations. The desensitized structure adopts an unexpected hourglass conformation, suggesting a gating mechanism closer related to cation-selective channels. Structural analysis and mutagenesis identify extracellular histidine and glutamic acid residues that impact the pH-sensitivity, likely contributing to a broader pH-sensing network. Ivermectin-bound structures reveal pH-dependent modulation, enhancing open-state prevalence at pH 9 and enabling atypical activation at pH 6.5. These findings offer initial insights into SsCl's pH-sensitivity and ivermectin's activity, informing next-generation antiparasitic design. PubMed: 41820392DOI: 10.1038/s41467-026-70575-0 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (4.24 Å) |
Structure validation
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