Abstract
ATP-sensitive potassium channels (KATP) couple intracellular ATP levels with membrane excitability. These channels play crucial roles in many essential physiological processes and have been implicated extensively in a spectrum of metabolic diseases and disorders. To gain insight into the mechanism of KATP, we elucidated the structure of a hetero-octameric pancreatic KATP channel in complex with a non-competitive inhibitor glibenclamide by single-particle cryoelectron microscopy to 5.6-Å resolution. The structure shows that four SUR1 regulatory subunits locate peripherally and dock onto the central Kir6.2 channel tetramer through the SUR1 TMD0-L0 fragment. Glibenclamide-bound SUR1 uses TMD0-L0 fragment to stabilize Kir6.2 channel in a closed conformation. In another structural population, a putative co-purified phosphatidylinositol 4,5-bisphosphate (PIP2) molecule uncouples Kir6.2 from glibenclamide-bound SUR1. These structural observations suggest a molecular mechanism for KATP regulation by anti-diabetic sulfonylurea drugs, intracellular adenosine nucleotide concentrations, and PIP2 lipid.
Keywords
ABCC
K(ATP)
Kir
PIP(2)
SUR
glibenclamide
sulfonylurea
MeSH Terms
ATP Binding Cassette Transporter, Subfamily B/chemistry,metabolism
Animals
Cryoelectron Microscopy
Humans
Hydrolases/chemistry,metabolism
KATP Channels/chemistry,metabolism
Mammals/metabolism
Mesocricetus
Mice
Models, Molecular
Phosphoinositide Phospholipase C/chemistry,metabolism
Potassium Channels, Inwardly Rectifying/chemistry,metabolism
Sulfonylurea Receptors/chemistry,metabolism
Chemicals
ATP Binding Cassette Transporter, Subfamily B
KATP Channels
Kir6.2 channel
Potassium Channels, Inwardly Rectifying
Sulfonylurea Receptors
Hydrolases
Phosphoinositide Phospholipase C
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Li Ningning
State Key Laboratory of Membrane Biology, Institute of Molecular Medicine, Peking-Tsinghua Center for Life Sciences, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking University, Beijing 100871, China; School of Life Sciences, Peking University, Beijing 100871, China.
Wu Jing-Xiang
State Key Laboratory of Membrane Biology, Institute of Molecular Medicine, Peking-Tsinghua Center for Life Sciences, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking University, Beijing 100871, China.
Ding Dian
State Key Laboratory of Membrane Biology, Institute of Molecular Medicine, Peking-Tsinghua Center for Life Sciences, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking University, Beijing 100871, China.
Cheng Jiaxuan
Ministry of Education Key Laboratory of Protein Sciences, Beijing Advanced Innovation Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Gao Ning
Ministry of Education Key Laboratory of Protein Sciences, Beijing Advanced Innovation Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China. Electronic address:
[email protected].
Chen Lei
State Key Laboratory of Membrane Biology, Institute of Molecular Medicine, Peking-Tsinghua Center for Life Sciences, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Peking University, Beijing 100871, China. Electronic address:
[email protected].