Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10954409 | Journal of Molecular and Cellular Cardiology | 2005 | 20 Pages |
Abstract
A multidisciplinary effort over twenty years has provided deep insight into the nature of KATP channels. First discovered in cardiomyocytes and pancreatic β-cells, as ubiquitous sensors of the ADP/ATP ratio they are implicated in multiple disorders characterized by the uncoupling of excitation from metabolism. Composed of two disparate subunits these large octameric channels present a formidable challenge to scientists interested in understanding mechanism in physical, chemical, and structural terms. Post-cloning studies have defined the domains and interactions, within and between the nucleotide-inhibited KIR pore and nucleotide-stimulated, drug-binding core of the ATP-Binding Cassette (ABC) regulatory subunits, that control channel assembly and gating. Determination of the three-dimensional structures of the bacterial prototypes of the channel subunits allowed homology modeling and has provided increasingly detailed mechanistic understanding. Here I review the early electrophysiology and molecular biology of KATP channels, cover biophysical principles governing their single channel kinetics, integrate this with current efforts to understand ligand-recognition and gating within the pore and SUR core, and propose a mechanism of coupling based on recent identification of a SUR gatekeeper module and first composite models of (SUR/KIR 6.0)4 complexes. This mechanism, based on interactions between inter-KIR subunit ATP-binding pockets and a unique bi-directional regulatory apparatus comprised of elements from the gatekeeper and KIR amino terminus, provides a molecular perspective for understanding the biophysical basis underlying the polar effects of pathogenic mutations in KATP channel subunits.
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Authors
Andrey P. Babenko,