In vitro reconstitution of eukaryotic ion channels using droplet interface bilayers.
J Am Chem Soc 133:24 (2011) 9370-9375
Abstract:
The ability to routinely study eukaryotic ion channels in a synthetic lipid environment would have a major impact on our understanding of how different lipids influence ion channel function. Here, we describe a straightforward, detergent-free method for the in vitro reconstitution of eukaryotic ion channels and ionotropic receptors into droplet interface bilayers and measure their electrical activity at both the macroscopic and single-channel level. We explore the general applicability of this method by reconstitution of channels from a wide range of sources including recombinant cell lines and native tissues, as well as preparations that are difficult to study by conventional methods including erythrocytes and mitochondria.Functional Analysis of Mutations in the TRESK K2P Potassium Channel Associated with ‘migraine with Aura’
Biophysical Journal Elsevier 100:3 (2011) 279a
Identification of Gating Mutations in the Trek-1 k2p Potassium Channel by Functional Complementation in K+ uptake Deficient Yeast
Biophysical Journal Elsevier 100:3 (2011) 279a-280a
PIP2-Binding to an Open State Model of Kir1.1 Probed by Multiscale Biomolecular Simulations
Biophysical Journal Elsevier 100:3 (2011) 431a
The Kir5.1 Potassium Channel is an Important Determinant of Neuronal PCO2/pH Sensitivity
Biophysical Journal Elsevier 100:3 (2011) 430a