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Patch clamp measurements on Xenopus laevis oocytes: Currents through endogenous channels and implanted acetylcholine receptor and sodium channels

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons95970

Witzemann,  Veit
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;
Working Group Witzemann / Koenen, Max Planck Institute for Medical Research, Max Planck Society;
Molecular anatomy of the neuromuscular junction, Max Planck Institute for Medical Research, Max Planck Society;
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons95089

Sakmann,  Bert
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Methfessel, C., Witzemann, V., Takahashi, T., Mishina, M., Numa, S., & Sakmann, B. (1986). Patch clamp measurements on Xenopus laevis oocytes: Currents through endogenous channels and implanted acetylcholine receptor and sodium channels. Pfluegers Archiv European Journal of Physiology, 407(6), 577-588. Retrieved from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd%3DRetrieve%26db%3DPubMed%26list_uids%3D2432468%26dopt%3DAbstract.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0019-AEEC-E
Abstract
Functional acetylcholine receptor (AChR) and sodium channels were expressed in the membrane of Xenopus laevis oocytes following injection with poly(A)+−mRNA extracted from denervated rat leg muscle. Whole−cell currents, activated by acetylcholine or by depolarizing voltage steps had properties comparable to those observed in rat muscle. Oocytes injected with specific mRNA, transcribed from cDNA templates and coding for the AChR of Torpedo electric organ, expressed functional AChR channels at a much higher density. Single−channel currents were recorded from the oocyte plasma membrane following removal of the follicle cell layer and the vitelline membrane from the oocyte. The follicle cell layer was removed enzymatically with collagenase. The vitelline membrane was removed either mechanically after briefly exposing the oocyte to a hypertonic solution, or by enzyme treatment with pronase. Stretch activated (s.a.) currents were observed in most recordings from cell−attached patches obtained with standard patch pipettes. S.a.−currents were evoked by negative or positive pressure (greater than or equal to 5 mbar) applied to the inside of the pipette, and were observed in both normal and mRNA injected oocytes indicating that they are endogenous to the oocyte membrane. The s.a.−channels are cation selective and their conductance is 28 pS in normal frog Ringers solution (20 +/− 1 degree C). Their gating is voltage dependent, and their open probability increases toward more positive membrane potentials. The density of s.a.−channels is estimated to be 0.5−2 channels per micron 2 of oocyte plasma membrane. In cell−attached patches s.a.−currents are observed much less frequently when current measurement is restricted to smaller patches of 3−5 micron 2 area using thick−walled pipettes with narrow tips. In outside−out patches s.a.−currents occur much less frequently than in cell−attached or inside−out patches. AChR−channel and sodium channel currents were observed only in a minority of patches from oocytes injected with poly(A)+−mRNA from rat muscle. AChR−channel currents were seen in all patches of oocytes injected with specific mRNA coding for Torpedo AChR. In normal frog Ringers solution (20 +/− 2 degrees C) the conductance of implanted rat muscle AChR−channels was 38 pS and that of sodium channels 20 pS. The conductance of implanted Torpedo AChR channels was 40 pS. The conductance of implanted channels was similar in cell−attached and in cell−free patches