The gramicidin-perforated patch-clamp technique is indispensable for recording neuronal activities without changing the intracellular Cl concentration. Conventionally, gramicidin contained in the pipette fluid is delivered to the cell membrane by passive diffusion. Gramicidin deposited on the pipette orifice sometimes hampers giga-seal formation, and perforation progresses only slowly. These problems may be circumvented by delivering a high concentration of gramicidin from an intra-pipette capillary after a giga-seal is formed. We herein describe the detailed protocol of this improved method. This protocol would greatly facilitate the investigation of Cl gradient-dependent neuronal activities.
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http://dx.doi.org/10.1016/j.neures.2024.05.002 | DOI Listing |
Neurosci Res
October 2024
Laboratory for Biological Information Processing, Faculty of Engineering, University of Toyama, 3190 Gofuku, Toyama, Toyama 930-8555, Japan. Electronic address:
The gramicidin-perforated patch-clamp technique is indispensable for recording neuronal activities without changing the intracellular Cl concentration. Conventionally, gramicidin contained in the pipette fluid is delivered to the cell membrane by passive diffusion. Gramicidin deposited on the pipette orifice sometimes hampers giga-seal formation, and perforation progresses only slowly.
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