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8K1Q

Human TWIK-related acid-sensitive potassium channel TASK3 at pH 6.0, 5 mM KCl and 135 mM NaCl

Summary for 8K1Q
Entry DOI10.2210/pdb8k1q/pdb
EMDB information36799
DescriptorPotassium channel subfamily K member 9, CHOLESTEROL HEMISUCCINATE, POTASSIUM ION, ... (4 entities in total)
Functional Keywordsacid-sensitive, potassium ion channel, c-type, gating mechanism, membrane protein
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight65345.03
Authors
Chen, S.,Lin, H. (deposition date: 2023-07-11, release date: 2024-04-17, Last modification date: 2024-05-01)
Primary citationLin, H.,Li, J.,Zhang, Q.,Yang, H.,Chen, S.
C-type inactivation and proton modulation mechanisms of the TASK3 channel.
Proc.Natl.Acad.Sci.USA, 121:e2320345121-e2320345121, 2024
Cited by
PubMed Abstract: The TWIK-related acid-sensitive K channel 3 (TASK3) belongs to the two-pore domain (K2P) potassium channel family, which regulates cell excitability by mediating a constitutive "leak" potassium efflux in the nervous system. Extracellular acidification inhibits TASK3 channel, but the molecular mechanism by which channel inactivation is coupled to pH decrease remains unclear. Here, we report the cryo-electron microscopy structures of human TASK3 at neutral and acidic pH. Structural comparison revealed selectivity filter (SF) rearrangements upon acidification, characteristic of C-type inactivation, but with a unique structural basis. The extracellular mouth of the SF was prominently dilated and simultaneously blocked by a hydrophobic gate. His98 protonation shifted the conformational equilibrium between the conductive and C-type inactivated SF toward the latter by engaging a cation-π interaction with Trp78, consistent with molecular dynamics simulations and electrophysiological experiments. Our work illustrated how TASK3 is gated in response to extracellular pH change and implies how physiological stimuli might directly modulate the C-type gating of K2P channels.
PubMed: 38630723
DOI: 10.1073/pnas.2320345121
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.68 Å)
Structure validation

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數據於2024-11-06公開中

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