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Biophys J, December 2002, p. 3296-3303, Vol. 83, No. 6





*Division of Medicine and
National Heart and Lung
Institute, Imperial College of Science, Technology and Medicine, MRC
Clinical Sciences Centre, London W12 0NN, United Kingdom;
Department of Physiological Sciences, University of
Newcastle, Newcastle upon Tyne, United Kingdom;
§Department of Pharmacology, University College London,
London, United Kingdom; ¶Department of Development
Genetics and Molecular Physiology, Institute of Biotechnology, National
Autonomous University of Mexico, Cuernavaca, Morelos, Mexico;
Office of Naval Research, Arlington, Virginia USA; and
**Department of Chemistry, Cambridge University, Cambridge, United
Kingdom
We have developed a scanning patch-clamp technique that
facilitates single-channel recording from small cells and submicron cellular structures that are inaccessible by conventional methods. The
scanning patch-clamp technique combines scanning ion conductance microscopy and patch-clamp recording through a single glass nanopipette probe. In this method the nanopipette is first scanned over a cell
surface, using current feedback, to obtain a high-resolution topographic image. This same pipette is then used to make the patch-clamp recording. Because image information is obtained via the
patch electrode it can be used to position the pipette onto a cell with
nanometer precision. The utility of this technique is demonstrated by
obtaining ion channel recordings from the top of epithelial microvilli
and openings of cardiomyocyte T-tubules. Furthermore, for the first
time we have demonstrated that it is possible to record ion channels
from very small cells, such as sperm cells, under physiological
conditions as well as record from cellular microstructures such as
submicron neuronal processes.
Biophys J, December 2002, p. 3296-3303, Vol. 83, No. 6
© 2002 by the Biophysical Society 0006-3495/02/12/3296/08 $2.00
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