How Do Amphiphiles Form Ion-Conducting Channels in Membranes? Lessons from Linear Oligoesters

THOMAS M. FYLES

ACCOUNTS OF CHEMICAL RESEARCH

The X-ray crystal structures of biological ion channels are exquisitely complex, but not all natural products capable of forming ion-conducting channels are equally elaborate. Examples such as the peptides gramicidin or alamethicin or the polyene antibiotics amphotericin and nystatin clearly form well-defined channels without requiring a massive protein superstructure. These molecules form the starting point for a supramolecular chemistry challenge: how to create synthetic compounds and systems that catalyze the translocation of ionic species across bilayer membranes mimicking naturally occurring channels. Over the past three decades, supramolecular chemists have developed numerous examples of systems with transport rates and efficiencies that rival natural channels. As the field developed, researchers discovered many compounds that are functional for ion transport but bear very little resemblance to any imagined architectures of ion channels. We and others have followed these lead compounds extensively in a quest to focus on the mechanisms such simple compounds use to achieve their function. These compounds show all the hallmarks of ion channels including high activity, ion specificity, regular time-dependent conductance changes, and in some cases higher-order phenomena such as voltage-dependent activity.