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.
Original language | English |
---|---|
Pages (from-to) | 9370-9375 |
Number of pages | 6 |
Journal | J. Am. Chem. Soc. |
Volume | 133 |
Issue number | 24 |
DOIs | |
Publication status | Published - 1 Jun 2011 |