Optical control of ion channel gating could permit the functional manipulat
ion of excitable cells. We wished to examine the feasibility of using optic
al switching of ion-dipole interactions as a means of switching ion flux in
channels. We prepared an analogue of the ion channel gramicidin A in which
an azobenzene side chain was substituted for a valine side chain at positi
on 1. The dipole moment of the azobenzene group can be reversibly switched
between approximately 3 and 0 D by cis-trans photoisomerization. The observ
ed conductance properties of the modified channels can be understood in ter
ms of (switchable) ion-dipole interactions that control the height of the c
entral barrier for Cs+ and Na+ movement through the pore. The predictable b
ehavior of the system implies that larger dipole changes or changes closer
to the central axis of the pore might effect complete gating.