Patch clamp

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Patch clamp technique is technique in electrophysiology that allows the study of individual ion channels in cells. The technique is used to study excitable cells such as neurons, muscle fibers and the beta cells of the pancreas. In classical patch clamp technique, the electrode used is a glass pipette, but planar patch clamp uses a flat surface punctured with tiny holes.

Patch clamp technique is a refinement of the voltage clamp. Erwin Neher and Bert Sakmann developed the patch clamp in the late 1970s and early 1980s. They received the Nobel Prize in Physiology or Medicine in 1991 for this work.

1 Basic technique
2 Variations
3 See also
4 References

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Basic technique

Image:Patchclamp1.png Patch clamp traditionally uses a glass pipette with a tip diameter of about one micrometre, and made such that the tip forms a smooth surfaced circle, rather than a sharp point. This style of electrode is known as a "patch clamp electrode" as distinct from a "sharp microelectrode" used to impale cells in traditional intracellular recordings. The interior of the pipette is filled with a solution that approximates the extracellular fluid. A metal electrode in contact with this solution conducts the electrical changes to a voltage clamp amplifier. During the experiment, the researcher can manipulate the contents of this solution or add drugs to study the ion channels under different condtions. The patch clamp electrode is pressed against a cell membrane and suction is applied to the inside of the electrode to pull the cell's membrane inside the tip of the electrode. The suction causes the cell to form a tight seal with the electrode (a so-called "gigaohm seal", since the electrical resistance of that seal is in excess of a gigaohm).

Unlike traditional voltage clamp recordings, patch clamp recording uses a single electrode to voltage clamp a cell. This allows a researcher to keep the voltage constant while observing changes in current. Alternately, the cell can be current clamped, keeping current constant while observing changes in membrane voltage.

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Variations

Several variations of the basic technique can be applied, depending on what the researcher wants to study. The inside-out and outside-out techniques are called "excised patch" techniques, because the patch is excised (removed) from the main body of the cell. Cell-attached and both excised patch techniques are used to study the behavior of ion channels on the section of membrane attached to the electrode, while whole-cell patch and perforated patch allow the researcher to study the electrical behavior of the entire cell.

Cell-attached patch: The electrode remains sealed to the patch of membrane. This allows for the recording of currents through single ion channels in that patch of membrane.
"Inside-out" patch: The electrode is quickly withdrawn from the cell, thus ripping the patch of membrane off the cell, leaving the patch of membrane attached to the electrode exposing the [[intracellular] surface of the membrane to the external media. This is useful when an experimenter wishes to manipulate the environment affecting the inside of ion channels.
"Outside-out" patch: The electrode is slowly withdrawn from the cell, allowing a bulb of membrane to bleb out from the cell. When the electrode is pulled far enough away, this bleb will part from the cell and reform as a ball of membrane on the end of the electrode, with the outside of the membrane being the surface of the ball. Outside-out patching gives the experimenter the opportunity to examine the properties of an ion channel when it is protected from the outside environment, but not in contact with its usual environment.
Whole-cell recording or whole-cell patch: The electrode is left in place, but more suction is applied to rupture the portion of the cell's membrane that is inside the electrode, thus providing access to the intracellular space of the cell. The advantage of whole-cell patch clamp recording over sharp microelectrode recording in that larger opening at the tip of the patch clamp electrode provides lower resisitance and thus better electrical access to the inside of the cell. A disadvantage of this technique is that the volume of the electrode is larger than the cell, so the soluble contents of the cell's interior will slowly be replaced by the contents of the electrode. This is referred to as the electrode "dialyzing" the cell's contents. Thus, any properties of the cell that depend soluble intracellular contents will be altered. Generally speaking, there is a "grace period" at the beginning of a whole-cell recording, lasting approximately 10 minutes, when one can take measurements before the cell has been dialyzed. Whole-cell recordings involve recording currents through multiple channels at once.
Perforated patch: In this variation of whole-cell recording, the experimenter forms the gigaohm seal, then adds a new solution to the electrode containing small amounts of an antibiotic, such as Amphothericin-B or Gramicidin into the electrode solution to punch small perforations on the bit of membrane attached to the electrode. This has the advantage of reducing the dialysis of the cell that occurs in whole cell recordings, but also has several disadvantages. First, the access resistance is higher (access resistance being the sum of the electrode resistance and the resistance at the electrode-cell junction). This will decrease current resolution, increase recording noise, and magnify any series resistance error. Second, it can take a significant amount of time (10-30 minutes) for the antibiotic to perforate the membrane. Third, the membrane under the electrode tip is weakened by the perforations formed by the antibiotic and tends to rupture. When the patch ruptures, the recording is essentially in whole-cell mode, except with antibiotic inside the cell. All of these problems tend to limit the time-length of experiments, and so this technique is most appropriate for short-duration experiments of about an hour.