Molecular structure of human KATP in complex with ATP and ADP

Elife. 2017 Dec 29:6:e32481. doi: 10.7554/eLife.32481.

Abstract

In many excitable cells, KATP channels respond to intracellular adenosine nucleotides: ATP inhibits while ADP activates. We present two structures of the human pancreatic KATP channel, containing the ABC transporter SUR1 and the inward-rectifier K+ channel Kir6.2, in the presence of Mg2+ and nucleotides. These structures, referred to as quatrefoil and propeller forms, were determined by single-particle cryo-EM at 3.9 Å and 5.6 Å, respectively. In both forms, ATP occupies the inhibitory site in Kir6.2. The nucleotide-binding domains of SUR1 are dimerized with Mg2+-ATP in the degenerate site and Mg2+-ADP in the consensus site. A lasso extension forms an interface between SUR1 and Kir6.2 adjacent to the ATP site in the propeller form and is disrupted in the quatrefoil form. These structures support the role of SUR1 as an ADP sensor and highlight the lasso extension as a key regulatory element in ADP's ability to override ATP inhibition.

Keywords: ADP; ATP; KATP; Kir6.2; SUR1; biophysics; cryo-EM; neuroscience; none; structural biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Diphosphate / chemistry*
  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / chemistry*
  • Adenosine Triphosphate / metabolism
  • Cryoelectron Microscopy
  • Humans
  • Magnesium / chemistry
  • Magnesium / metabolism
  • Potassium Channels, Inwardly Rectifying / chemistry*
  • Potassium Channels, Inwardly Rectifying / metabolism
  • Protein Binding
  • Protein Conformation
  • Sulfonylurea Receptors / chemistry*
  • Sulfonylurea Receptors / metabolism

Substances

  • ABCC8 protein, human
  • Kir6.2 channel
  • Potassium Channels, Inwardly Rectifying
  • Sulfonylurea Receptors
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Magnesium