Minimizing Cytosol Dilution in Whole-Cell Patch-Clamp Experiments

During a conventional whole-cell patch clamp experiment, diffusible cytosolic ions or molecules absent in the pipette solution can become diluted by a factor of one million or more, leading to diminished current or fluorescent signals. Existing methods to prevent or limit cytosol diffusion include reducing the diameter of the pipette’s orifice, adding cytosolic extract or physiological entities to the pipette solution, and use of the perforated patch clamp configuration. The first method introduces measurement error in recorded signals from increased series resistance and the latter two are cumbersome to perform. In addition, most perforated patch configurations, prevent investigators from using test compounds in the pipette solution. We present a method to overcome these limitations by minimizing cytosol dilution using a novel pipette holder. After obtaining cell-attached configuration conventionally with a large reservoir of pipette solution, we displace most of the pipette solution with mineral oil before going whole-cell thus minimizing cytosol dilution. To accomplish this requires a suction line and two Ag/AgCl electrodes inside the pipette. Testing our novel pipette holder with Chinese Hamster Ovarian cells, we demonstrate cytosol dilution factors between 76 and 234. For large cells with somas greater than 40 μm, cytosol dilution factors of 10 or less are achievable.