Ligand-mediated Structural Dynamics of a Mammalian Pancreatic KATP Channel

J Mol Biol. 2022 Oct 15;434(19):167789. doi: 10.1016/j.jmb.2022.167789. Epub 2022 Aug 11.

Abstract

Regulation of pancreatic KATP channels involves orchestrated interactions of their subunits, Kir6.2 and SUR1, and ligands. Previously we reported KATP channel cryo-EM structures in the presence and absence of pharmacological inhibitors and ATP, focusing on the mechanisms by which inhibitors act as pharmacological chaperones of KATP channels (Martin et al., 2019). Here we analyzed the same cryo-EM datasets with a focus on channel conformational dynamics to elucidate structural correlates pertinent to ligand interactions and channel gating. We found pharmacological inhibitors and ATP enrich a channel conformation in which the Kir6.2 cytoplasmic domain is closely associated with the transmembrane domain, while depleting one where the Kir6.2 cytoplasmic domain is extended away into the cytoplasm. This conformational change remodels a network of intra- and inter-subunit interactions as well as the ATP and PIP2 binding pockets. The structures resolved key contacts between the distal N-terminus of Kir6.2 and SUR1's ABC module involving residues implicated in channel function and showed a SUR1 residue, K134, participates in PIP2 binding. Molecular dynamics simulations revealed two Kir6.2 residues, K39 and R54, that mediate both ATP and PIP2 binding, suggesting a mechanism for competitive gating by ATP and PIP2.

Keywords: ATP-sensitive potassium channel; congenital hyperinsulinism; cryoEM structure; inward rectifying potassium channel; neonatal diabetes; sulfonylurea receptor.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Ligands
  • Mammals / metabolism
  • Potassium Channels, Inwardly Rectifying* / chemistry
  • Potassium Channels, Inwardly Rectifying* / metabolism
  • Sulfonylurea Receptors / chemistry
  • Sulfonylurea Receptors / metabolism

Substances

  • Ligands
  • Potassium Channels, Inwardly Rectifying
  • Sulfonylurea Receptors
  • Adenosine Triphosphate