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9M05

Cryo-EM structure of dVGAC complexed with iodide

Summary for 9M05
Entry DOI10.2210/pdb9m05/pdb
Related8YQ5 8YQ6
EMDB information39496 39497 63538
Descriptorde novo designed ion channel, IODIDE ION (2 entities in total)
Functional Keywordsde novo design, ion channels, de novo protein
Biological sourcesynthetic construct
Total number of polymer chains5
Total formula weight132375.64
Authors
Lu, P.L.,Zhou, C. (deposition date: 2025-02-23, release date: 2025-10-29, Last modification date: 2026-01-07)
Primary citationZhou, C.,Li, H.,Wang, J.,Qian, C.,Xiong, H.,Chu, Z.,Shao, Q.,Li, X.,Sun, S.,Sun, K.,Zhu, A.,Wang, J.,Jin, X.,Yang, F.,Gamal El-Din, T.M.,Li, B.,Huang, J.,Wu, K.,Lu, P.
De novo designed voltage-gated anion channels suppress neuron firing.
Cell, 188:7495-, 2025
Cited by
PubMed Abstract: Design of ion channels responsive to environmental cues has significant implications in modulating cellular activities and sensor development, but it remains a significant challenge due to the complexities involved in designing stimuli-induced conformational changes in proteins. Here, we report the accurate de novo design of voltage-gated anion channels, namely dVGACs. dVGACs adopt a 15-helix pentameric architecture featuring arginine constrictions within the transmembrane span and show voltage-dependent anions currents in patch-clamp experiments. Cryo-electron microscopy (cryo-EM) structures of dVGACs closely align with the design models. Cryo-EM structures and molecular dynamics simulations suggest that the arginine constrictions undergo voltage-induced conformational changes, serving as both a voltage sensor and a selectivity filter as designed. Notably, the anion selectivity and voltage sensitivity of dVGACs can be tuned through targeted mutations for suppressing neuronal firing in situ. The ability to create ion channels with custom-designed conformational changes refreshes our insights into membrane biophysics and unveils diverse potential applications.
PubMed: 41106381
DOI: 10.1016/j.cell.2025.09.023
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.72 Å)
Structure validation

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